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  #161  
Old Saturday, October 17, 2009
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Default Sex-Linked Inheritance

Sex-Linked Inheritance

In humans, sex is determined by the twenty-third pair of chromosomes known as the sex chromosomes. If at conception you have two X-shaped (XX) chromosomes you are destined to be a female. If you have an X and a Y-shaped chromosome (XY) you are destined to be male. Since the X and the Y chromosomes differ in the information they carry, any gene found on the X chromosome is referred to as a sex-linked gene. Women will have two alleles for sex-linked genes while men will only have one.






Example:
Hemophilia is a sex-linked trait. A person with hemophilia is lacking certain proteins that are necessary for normal blood clotting. Since hemophilia is a recessive trait, use N for normal and n for hemophilia. A woman who is heterozygous for hemophilia (a carrier) marries a normal man. What are the possible genotypes of their offspring?

Example:
Examine the following pedigree chart of colorblindness. In humans, color blindness is caused by a recessive sex-linked allele. On the diagram, label the genotypes of the individuals.



In humans, there are hundreds of genes located on the X chromosome that have no counterpart on the Y chromosome. The traits governed by these genes thus show sex-linked inheritance. This type of inheritance has certain unique characteristics, which include the following: (1) There is no male-to-male (father-to-son) transmission, since sons will, by definition, inherit the Y rather than the X chromosome. (2) The carrier female (heterozygote) has a 50 percent chance of passing the mutant gene to each of her children; sons who inherit the mutant gene will be hemizygotes and will manifest the trait, while daughters who receive the mutant gene will be unaffected carriers. (3) Males with the trait will pass the gene on to all of their daughters, who will be carriers. (4) Most sex-linked traits are recessively inherited, so that heterozygous females generally do not display the trait. The table lists some sex-linked conditions.


The figure shows a pedigree of a family in which a mutant gene for hemophilia A, a sex-linked recessive disease, is segregating. Hemophilia A gained notoriety in early studies of human genetics because it affected at least 10 males among the descendants of Queen Victoria, who was a carrier Hemophilia A, the most widespread form of hemophilia, results from a mutation in the gene encoding clotting factor VIII. Because of this mutation, affected males cannot produce functional factor VIII, so that their blood fails to clot properly, leading to significant and potentially life-threatening loss of blood after even minor injuries. Bleeding into joints commonly occurs as well and may be crippling. Therapy consists of avoiding trauma and of administering injections of purified factor VIII, which was once isolated from outdated human blood donations but can now be made in large amounts through recombinant DNA technology.
Although heterozygous female carriers of X-linked recessive mutations generally do not exhibit traits characteristic of the disorder, cases of mild or partial phenotypic expression in female carriers have been reported, resulting from nonrandom X inactivation.



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  #162  
Old Sunday, October 18, 2009
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Default Test Cross

Test cross

Mendel devised a system of conducting verification for the results obtained by him. It is known as test cross. It is a cross between F1 plant and the recessive parent. A test cross-conducted for the monohybrid inheritance results in the two opposite characters expressing in a ratio of 1:1.

Similarly, a test cross-conducted for the dihybrid inheritance results in the expression of the two parental combinations and the two recombinations appear in the ratio 1:1:1:1.





Significance of Test Cross

  • Test cross can be used to determine the genotype of the F1 plant.
  • The test cross can be used to support the idea that the reappearance of the recessive character in the F2 generation is due to the heterozygous condition of the F1 plant.
  • The test can be used to verify whether any given pair of characters can be alleles (contrasting characters).
Back Cross

If an F1 individual or an individual of F2 or F3 generations is crossed with any one of the parents it is called a back cross.
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  #163  
Old Monday, October 19, 2009
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Default Rh-Factor

Rh factor

The Rh factor is an antigen (a protein) that is found on the surface of the red blood cell. Along with the A and B antigens it comprises the major scheme we use for "typing" or classifying human blood for compatibility for transfusion.

The term "Rh factor" is short for Rhesus factor. It seems we share this antigen with our relatives in the primate world, the rhesus monkeys.

The antigen is either there, or it is not. This is determined by the presence or absence of a single gene. We can test for the presence of the antigen by adding artificially produced antibodies to a mixture of the patient's red cells. If they form clumps, we know that the antibody is present on the red cells. We term this blood Rh positive. If the antigen is not present (and the cells don't clump), we designate the blood type as Rh negative.

About the Rh Factor


People with different blood types have proteins specific to that blood type on the surfaces of their red blood cells (RBCs). There are four blood types — A, B, AB, and O.

Each of the four blood types is additionally classified according to the presence of another protein on the surface of RBCs that indicates the Rh factor. If you carry this protein, you are Rh positive. If you don't carry the protein, you are Rh negative.

Most people — about 85% — are Rh positive. But if a woman who is Rh negative and a man who is Rh positive conceive a baby, there is the potential for a baby to have a health problem. The baby growing inside the Rh-negative mother may have Rh-positive blood, inherited from the father. Approximately half of the children born to an Rh-negative mother and Rh-positive father will be Rh positive.

Rh incompatibility usually isn't a problem if it's the mother's first pregnancy because, unless there's some sort of abnormality, the fetus's blood does not normally enter the mother's circulatory system during the course of the pregnancy.

However, during delivery, the mother's and baby's blood can intermingle. If this happens, the mother's body recognizes the Rh protein as a foreign substance and can begin producing antibodies (protein molecules in the immune system that recognize, and later work to destroy, foreign substances) against the Rh proteins introduced into her blood.

Other ways Rh-negative pregnant women can be exposed to the Rh protein that might cause antibody production include blood transfusions with Rh-positive blood, miscarriage, and ectopic pregnancy.

Rh antibodies are harmless until the mother's second or later pregnancies. If she is ever carrying another Rh-positive child, her Rh antibodies will recognize the Rh proteins on the surface of the baby's blood cells as foreign, and pass into the baby's bloodstream and attack those cells. This can lead to swelling and rupture of the baby's RBCs. A baby's blood count can get dangerously low when this condition, known as hemolytic or Rh disease of the newborn, occurs.


An antigen present on the red blood cells of about 85% of people. Called Rh because it was first identified in the blood of rhesus monkeys. Persons with the factor are designated Rh-positive, those lacking the factor are designated Rh-negative.

Protein on surface of red blood cells in some blood types (Rh+) and absent in others (Rh-). Can cause erythroblastosis fetalis in second pregnancy if fetal/maternal blood of opposite groups mix on first pregnancy.

An additional blood factor found in the red blood cells. When it is absent, the person is said to be Rh negative.

A group of antigens found on the surface of red blood cells.

-----------------------
The two most important classifications to describe blood types in humans are ABO and the Rhesus factor (Rh factor). There are 46 other known antigens in humans, most of which are much rarer than ABO and Rh. Blood transfusions from incompatible groups can cause an immunological transfusion reaction, resulting in hemolytic anemia, renal failure, shock, and death. The ABO blood types also exist among chimpanzees and bonobos.

The phrases "blood group" and "blood type" are often used interchangeably, although this is not technically correct. "Blood group" is used to refer specifically to a person's ABO status, while "blood type" refers to both ABO and Rh factors. When typing blood, 'positive' and 'negative' refer to Rh status, not ABO status; thus, for instance, an "A-neg" person is somebody who has the A antigen but does not have the Rh antigen.

Blood type is determined by the antigens (epitopes) on the surface of a red blood cell. Some of these are proteins, while others are proteins with polysaccharides attached. The absence of some of these markers leads to production of antibodies against this marker. The exact reason why this happens is poorly understood, as generally an antigen needs to be present to elicit an immune response. Administration of the wrong blood type would lead to immediate destruction of the infused blood. The breakdown products cause acute medical illness; hence it is of vital importance that the blood types of the donor and receptor be properly matched.
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  #164  
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Default Polyploidy

Polyploidy

Polyploidy is the condition whereby a biological cell or organism has more than two homologous sets of chromosomes, with each set essentially coding for all the biological traits of the organism. A haploid (n) only has one set of chromosomes. A diploid cell (2n) has two sets of chromosomes. Polyploidy involves three or more times the haploid number of chromosomes. Polyploid types are termed according to the number of chromosome sets in the nucleus: triploid (three sets; 3n), tetraploid (four sets; 4n), pentaploid (five sets; 5n), hexaploid (six sets; 6n), and so on.

To define this further, homologous chromosomes are those non-identical chromosomes that contain information for the same biological features and contain the same genes at the same loci, but possibly different genetic information, called alleles, at those genes. For example, two chromosomes may have genes encoding eye color, but one may code for brown eyes, the other for blue. Non-homologous chromosomes, representing all the biological features of an organism, form one set, and the number of sets in a cell is called ploidy. In diploid organisms (most plants and animals), each homologous chromosome is inherited from a different parent. But polyploid organisms have more than two homologous chromosomes.

Typically, a gamete or reproductive cell is haploid, while the somatic or body cell of the organism is diploid. That is, a somatic cell has a paired set of chromosomes; the haploid reproductive cell has a single set of unpaired chromosomes, or one half the number of chromosomes of a somatic cell. In diploid organisms, sexual reproduction involves alternating haploid (n) and diploid (2n) phases, with fusion of haploid cells to produce a diploid organism. (See life cycle.) Some organisms, however, exhibit polyploidy, whereby there are more than two homologous sets of chromosomes.

In addition to being a natural phenomena, human beings have used polyploidy creatively to create seedless bananas, hybrids of different species (triticale, a hybrid of wheat and rye), and other desirable or more robust plants.

Note that haploidy is not restricted to sexual reproduction involving meiosis, but may also occur as a normal stage in an organism's life cycle, such as in ferns and fungi. In some instances not all the chromosomes are duplicated and the condition is called aneuploidy. Where an organism is normally diploid, some spontaneous aberrations may occur that are usually caused by a hampered cell division.



Polyploidy in animals and plants

Polyploidy occurs in some animals, such as goldfish, salmon, and salamanders.

However, polyploidy is especially common among ferns and flowering plants, including both wild and cultivated species. Wheat, for example, after millennia of hybridization and modification by humans, has strains that are diploid (two sets of chromosomes); tetraploid (four sets of chromosomes), with the common name of durum or macaroni wheat; and hexaploid (six sets of chromosomes), with the common name of bread wheat.

Many agriculturally important plants of the genus Brassica are also tetraploids. This genus, known as cabbages or mustards, includes turnips, brussels sprouts, cabbage, cauliflower, broccoli, mustard seed and other important crops. The Triangle of U is a theory, developed by a Woo Jang-choon, a Korean botanist who was working in Japan, that says the genomes of three ancestral species of Brassica combined to create the three common tetraploid species Brassica juncea (Indian mustard), Brassica napus (Rapeseed, rutabaga), and Brassica carinata (Ethiopian mustard).

Examples in animals are more common in the lower forms such as flatworms, leeches, and brine shrimp. Polyploid animals are often sterile, so they often reproduce by parthenogenesis, a form of asexual reproduction. Polyploid salamanders and lizards are also quite common and parthenogenetic. While mammalian liver cells are polyploid, rare instances of polyploid mammals are known, but most often result in prenatal death.

The only known exception to this rule is an octodontid rodent of Argentina's harsh desert regions, known as the Red Viscacha-Rat (Tympanoctomys barrerae), discovered by Milton Gallardo Narcisi. This rodent is not a rat, but kin to guinea pigs and chinchillas. Its "new" diploid [2n] number is 102 and so its cells are roughly twice normal size. Its closest living relation is Octomys mimax, the Andean Viscacha-Rat of the same family, whose 2n=56. It is surmised that an Octomys-like ancestor produced tetraploid (i.e., 4n=112) offspring that were, by virtue of their doubled chromosomes, reproductively isolated from their parents; but that these likely survived the ordinarily catastrophic effects of polyploidy in mammals by shedding (via chromosomal translocation or some similar mechanism) the "extra" set of sex chromosomes gained at this doubling.

Polyploidy can be induced in cell culture by some chemicals: the best known is colchicine, which can result in chromosome doubling, though its use may have other less obvious consequences as well.

Polyploid crops

In plant breeding, the induction of polyploids is a common technique to overcome the sterility of a hybrid species. Triticale is the hybrid of wheat (Triticum turgidum) and rye (Secale cereale). It combines sought-after characteristics of the parents, but the initial hybrids are sterile. After polyploidization, the hybrid becomes fertile and can thus be further propagated to become triticale.

Polyploid plants in general are more robust and sturdy than diploids. In the breeding of crops, those plants that are stronger and tougher are selected. Thus, many crops have unintentionally been bred to a higher level of ploidy:

* Triploid crops: banana, apple, ginger
* Tetraploid crops: durum or macaroni wheat, maize, cotton, potato, cabbage, leek, tobacco, peanut, kinnow, Pelargonium
* Hexaploid crops: chrysanthemum, bread wheat, triticale, oat
* Octaploid crops: strawberry, dahlia, pansies, sugar cane

Some crops are found in a variety of ploidy. Apples, tulips and lilies are commonly found as both diploid and as triploid. Daylilies (Hemerocallis) cultivars are available as either diploid or tetraploid. Kinnows can be tetraploid, diploid, or triploid.

In the case of bananas, while the original bananas contained rather large seeds, triploid (and thus seedless) cultivars have been selected for human consumption. Cultivated bananas are sterile (parthenocarpic), meaning that they do not produce viable seeds. Lacking seeds, another form of propagation is required. These are propagated asexually from offshoots of the plant.

Polyploidy in humans


Polyploidy occurs in humans in the form of triploidy (69,XXX) and tetraploidy (92,XXXX).

Triploidy occurs in about two to three percent of all human pregnancies and around 15 percent of miscarriages. The vast majority of triploid conceptions end as miscarriage and those that do survive to term typically die shortly after birth. In some cases, survival past birth may occur longer if there is mixoploidy, with both a diploid and a triploid cell population present.

Triploidy may be the result of either diandry (the extra haploid set is from the father) or digyny (the extra haploid set is from the mother). Diandry is almost always caused by the fertilization of an egg by two sperm (dispermy). Digyny is most commonly caused by either failure of one meiotic division during oogenesis leading to a diploid oocyte or failure to extrude one polar body from the oocyte.

Diandry appears to predominate among early miscarriages, while digyny predominates among triploidy that survives into the fetal period. However, among early miscarriages, digyny is also more common in those cases under 8.5 weeks gestational age or those in which an embryo is present.

There are also two distinct phenotypes in triploid placentas and fetuses that are dependent on the origin of the extra haploid set. In digyny, there is typically an asymmetric poorly grown fetus, with marked adrenal hypoplasia (incomplete or arrested development of the adrenal glands) and a very small placenta. In diandry, the fetus (when present) is typically normally grown or symmetrically growth restricted, with normal adrenal glands and an abnormally large cystic placenta that is called a partial hydatidiform mole. These parent-of-origin effects reflect the effects of genomic imprinting.

Complete tetraploidy is more rarely diagnosed than triploidy, but is observed in one to two percent of early miscarriages. However, some tetraploid cells are not uncommonly found in chromosome analysis at prenatal diagnosis and these are generally considered "harmless." It is not clear whether these tetraploid cells simply tend to arise during in vitro cell culture or whether they are also present in placental cells in vivo. There are, at any rate, very few clinical reports of fetuses/infants diagnosed with tetraploidy mosaicism.

Mixoploidy is quite commonly observed in human preimplantation embryos and includes haploid/diploid as well as diploid/tetraploid mixed cell populations. It is unknown whether these embryos fail to implant and are therefore rarely detected in ongoing pregnancies or if there is simply a selective process favoring the diploid cells.



Autopolyploidy


Autopolyploids are polyploids with chromosomes derived from a single species. Autopolyploids can arise from a spontaneous, naturally-occurring genome doubling (for example, the potato). Bananas and apples can be found as triploid autopolyploids.

Allopolyploidy

Allopolyploids are polyploids with chromosomes derived from different species. Triticale is an example of an allopolyploid, having six chromosome sets, four from wheat (Triticum turgidum) and two from rye (Secale cereale). Cabbage is a very interesting example of a fertile allotetraploid crop. Amphidiploid is another word for an allopolyploid.

The giant tree Sequoia sempervirens or Coast Redwood has a hexaploid (6n) genome, and is also thought to be autoallopolyploid (AAAABB).

Paleopolyploidy

Ancient genome duplications probably characterize all life. Duplication events that occurred long ago in the history of various lineages can be difficult to detect because of subsequent diploidization (such that a polyploid starts to behave cytogenetically as a diploid over time) as mutations and gene translations gradually make one copy of each chromosome unlike its other copy.

In many cases, these events can be inferred only through comparing sequenced genomes. Examples of unexpected but recently confirmed ancient genome duplications include the baker's yeast (Saccharomyces cerevisiae), mustard weed/thale cress (Arabidopsis thaliana), rice (Oryza sativa), and an early ancestor of the vertebrates (which includes the human lineage) and another near the origin of the teleost fishes. Angiosperms (flowering plants) may have paleopolyploidy in their ancestry. All eukaryotes probably have experienced a polyploidy event at some point in their evolutionary history.
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  #165  
Old Monday, October 19, 2009
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Default Polyploidy

Polyploidy

Cells (and their owners) are polyploid if they contain more than two haploid (n) sets of chromosomes; that is, their chromosome number is some multiple of n greater than the 2n content of diploid cells. For example, triploid (3n) and tetraploid cell (4n) cells are polyploid.
Polyploidy in plants

Polyploidy is very common in plants, especially in angiosperms. From 30% to 70% of today's angiosperms are thought to be polyploid. Species of coffee plant with 22, 44, 66, and 88 chromosomes are known. This suggests that the ancestral condition was a plant with a haploid (n) number of 11 and a diploid (2n) number of 22, from which evolved the different polyploid descendants.

In fact, the chromosome content of most plant groups suggests that the basic angiosperm genome consists of the genes on 7–11 chromosomes. Domestic wheat, with its 42 chromosomes, is probably hexaploid (6n), where n (the ancestral haploid number) was 7.

Polyploid plants not only have larger cells but the plants themselves are often larger. This has led to the deliberate creation of polyploid varieties of such plants as watermelons, marigolds, and snapdragons.
Origin of Polyploidy

Polyploidy has occurred often in the evolution of plants.
The process can begin if diploid (2n) gametes are formed. These can arise in at least two ways.

* The gametes may be formed by mitosis instead of meiosis.
* Plants, in contrast to animals, form germ cells (sperm and eggs) from somatic tissues. If the chromosome content of a precursor somatic cell has accidentally doubled (e.g., as a result of passing through S phase of the cell cycle without following up with mitosis and cytokinesis), then gametes containing 2n chromosomes are formed.
Polyploidy also occurs naturally in certain plant tissues.

* As the endosperm (3n) develops in corn kernels (Zea mays), its cells undergo successive rounds (as many as 5) of endoreplication producing nuclei that range as high as 96n.
* When rhizobia infect the roots of their legume host, they induce the infected cells to undergo endoreplication producing cells that can become 128n (from 6 rounds of endoreplication).

Polyploidy can also be induced in the plant breeding laboratory by treating dividing cells with colchicine. This drug disrupts microtubules and thus prevents the formation of a spindle. Consequently, the duplicated chromosomes fail to separate in mitosis. Onion cells exposed to colchicine for several days may have over 1000 chromosomes inside.
Polyploidy and Speciation

When a newly-arisen tetraploid (4n) plant tries to breed with its ancestral species (a backcross), triploid offspring are formed. These are sterile because they cannot form gametes with a balanced assortment of chromosomes.

However, the tetraploid plants can breed with each other. So in one generation, a new species has been formed.

Polyploidy even allows the formation of new species derived from different ancestors.

In 1928, the Russian plant geneticist Karpechenko produced a new species by crossing a cabbage with a radish. Although belonging to different genera (Brassica and Raphanus respectively), both parents have a diploid number of 18. Fusion of their respective gametes (n=9) produced mostly infertile hybrids.

However, a few fertile plants were formed, probably by the spontaneous doubling of the chromosome number in somatic cells that went on to form gametes (by meiosis). Thus these contained 18 chromosomes — a complete set of both cabbage (n=9) and radish (n=9) chromosomes.

Fusion of these gametes produced vigorous, fully-fertile, polyploid plants with 36 chromosomes. (Unfortunately, they had the roots of the cabbage and the leaves of the radish.)

These plants could breed with each other but not with either the cabbage or radish ancestors, so Karpechenko had produced a new species.
The process also occurs in nature. Three species in the mustard family appear to have arisen by hybridization and polyploidy from three other ancestral species:

* B. oleracea (cabbage, broccoli, etc.) hybridized with B. nigra (black mustard) → B. carinata (Abyssinian mustard).
* B. oleracea x B. campestris (turnips) → B. napus (rutabaga)
* B. nigra x B. campestris → B. juncea (leaf mustard)

Modern wheat and perhaps some of the other plants listed in the table above have probably evolved in a similar way.
Polyploidy in animals

Polyploidy is much rarer in animals. It is found in some insects, fishes, amphibians, and reptiles. Until recently, no polyploid mammal was known. However, the 23 September 1999 issue of Nature reports that a polyploid (tetraploid; 4n = 102) rat has been found in Argentina.

Polyploid cells are larger than diploid ones; not surprising in view of the increased amount of DNA in their nucleus. The liver cells of the Argentinian rat are larger than those of its diploid relatives, and its sperm are huge in comparison. Normal mammalian sperm heads contain some 3.3 picograms (10-12 g) of DNA; the sperm of the rat contains 9.2 pg.





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Polyploidy

The occurrence of related forms possessing chromosome numbers which are multiples of a basic number (n), the haploid number. Forms having 3n chromosomes are triploids; 4n, tetraploids; 5n, pentaploids, and so on. Autopolyploids are forms derived by the multiplication of chromosomes from a single diploid organism. As a result the homologous chromosomes come from the same source. These are distinguished from allopolyploids, which are forms derived from a hybrid between two diploid organisms. As a result, the homologous chromosomes come from different sources. About one-third of the species of vascular plants have originated at least partly by polyploidy, and as many more appear to have ancestries which involve ancient occurrences of polyploidy. The condition can be induced artificially with the drug colchicine and the production of polyploid individuals has become a valuable tool for plant breeding.

In addition to polyploid organisms in which all of the body cells contain multiples of the basic chromosome number, most plants and animals contain particular tissues that are polyploid or polytene. Both polyploid and polytene cells contain extra copies of DNA, but they differ in the physical appearance of the chromosomes. In polytene cells the replicated copies of the DNA remain physically associated to produce giant chromosomes that are continuously visible and have a banded pattern. The term polyploid has been applied to several types of cells: multinucleate cells; cells in which the chromosomes cyclically condense but do not undergo nuclear or cellular division (this process is termed endomitosis); and cells in which the chromosomes appear to be continually in interphase, yet the replicated chromosomes are not associated in visible polytene chromosomes
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  #166  
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Default Chromosome map

Chromosome map:
The chart of the linear array of genes on a chromosome.

A chromosome map can also refer to the visual appearance of a chromosome when stained and examined under a microscope. Particularly important are visually distinct regions, called light and dark bands, which give each of the chromosomes a unique appearance. This feature allows a person's chromosomes to be studied in a clinical test known as a karyotype, which allows scientists to look for chromosomal alterations.



Our genetic information is stored in 23 pairs of chromosomes that vary widely in size and shape. Chromosome 1 is the largest and is over three times bigger than chromosome 22. The 23rd pair of chromosomes are two special chromosomes, X and Y, that determine our sex. Females have a pair of X chromosomes (46, XX), whereas males have one X and one Y chromosomes (46, XY). Chromosomes are made of DNA, and genes are special units of chromosomal DNA. Each chromosome is a very long molecule, so it needs to be wrapped tightly around proteins for efficient packaging.

Near the center of each chromosome is its centromere, a narrow region that divides the chromosome into a long arm (q) and a short arm (p). We can further divide the chromosomes using special stains that produce stripes known as a banding pattern. Each chromosome has a distinct banding pattern, and each band is numbered to help identify a particular region of a chromosome. This method of mapping a gene to a particular band of the chromosome is called cytogenetic mapping. For example, the hemoglobin beta gene (HBB) is found on chromosome 11p15.4. This means that the HBB gene lies on the short arm (p) of chromosome 11 and is found at the band labeled 15.4.

With the advent of new techniques in DNA analysis, we are able to look at the chromosome in much greater detail. Whereas cytogenetic mapping gives a bird's eye view of the chromosome, more modern methods show DNA at a much higher resolution. The Human Genome Project aims to identify and sequence the ~30,000 genes in human DNA.

Chromosome mapping is the assignment of genes to specific locations on a chromosome. A gene map serves many important functions and is much like understanding the basic human anatomy to allow doctors to diagnose patients with disease. A doctor requires knowledge of where each organ is located as well as the function of this organ to understand disease. A map of the human genome will allow scientist to understand where genes are located so that its function within the human genome can be elucidated. A detailed chromosome map also provides methods to study how genes are segregated and how genetic heterogeneity (variation between a particular gene maternally inherited and the same gene with a slightly different sequence that is paternally inherited) can help identify disease genes. Gene mapping can provide clinicians with useful information regarding genes that are linked, or segregate closely together.

Scientists use several methods to map genes to the appropriate locations. These methods include family studies, somatic cell genetic methods, cytogenetic techniques, and gene dosage studies. Family studies are used to determine whether two different genes are linked close together on a chromosome. If these genes are linked, it means they are close together on the same chromosome. Additionally, the frequency with which the genes are linked is determined by recombination events (crossing over of the chromosomes during meiosis) between known locations or markers, and determines the linear order or genetic distance. In somatic cell genetic methods, chromosomes are lost from a special type of cell and the remaining chromosome that has one gene, but not a different gene, would suggest that they are located on different chromosomes. This method allows scientists to identify which chromosome contains the gene, and represents one of the first mapping methods used by scientists.

Cytogenetic techniques refer to utilization of karyotype preparations, a technique that allows scientists to visualize of chromosomes, using fluorescence so that a fluorescently-labeled gene will reveal where the gene is found on the chromosome. Gene dosage studies uses, for example, numerical abnormalities to determine indirectly the location of the gene on a chromosome. In Down syndrome, there can be three chromosome number 21 (Trisomy 21), resulting in three copies of the gene and therefore, three times as much protein. In this case, a gene can be localized to chromosome 21 if there is three times as much protein in a cell with three 21 chromosomes. In this method, the amount of deoxyribonucleic acid (DNA) is assumed to be directly proportional to the amount of protein.

Using these methods, various maps of chromosomes can be developed. These maps are called cytogenetic maps, linkage maps, physical maps, or a DNA sequence map. A cytogenetic map uses bands produced by a dye that stains chromosomes in a karyotpe and assigns genes to these bands. A linkage map, also referred to as a genetic map, orders genes along the DNA strand based on recombination frequency. Linkage mapping involves using two characteristics (and hence their responsible genes), both of which are present in one parent, combined with the frequency in which they occur together in the offspring to construct the map. For example, the Moravian-born Augustinian monk and science teacher Gregor Johann Mendel (1823–1884) studied the flower color and plant height of peas. He found that various heights were observed just as frequently with white flowers as with other colored flowers and similarly, dwarf plants occurred just as frequently with the two flower types. Mendel concluded that the forms of the two genes were transmitted from parent to offspring independently of each other. This later became known as the Law of Independent Assortment, a concept that enhanced chromosome mapping techniques. A physical map orders genes or markers along the DNA strand of a chromosome. Finally, a DNA sequence, strung together, is the most precise type of map in that it contains both coding (gene-containing) and noncoding DNA. It is felt that obtaining the complete DNA sequence from the genome of many different organisms will provide scientists with vital information that will unlock many biological mysteries.
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Genetic Engineering

Genetic engineering is a laboratory technique used by scientists to change the DNA of living organisms.

DNA is the blueprint for the individuality of an organism. The organism relies upon the information stored in its DNA for the management of every biochemical process. The life, growth and unique features of the organism depend on its DNA. The segments of DNA which have been associated with specific features or functions of an organism are called genes.

Molecular biologists have discovered many enzymes which change the structure of DNA in living organisms. Some of these enzymes can cut and join strands of DNA. Using such enzymes, scientists learned to cut specific genes from DNA and to build customized DNA using these genes. They also learned about vectors, strands of DNA such as viruses, which can infect a cell and insert themselves into its DNA.

With this knowledge, scientists started to build vectors which incorporated genes of their choosing and used the new vectors to insert these genes into the DNA of living organisms. Genetic engineers believe they can improve the foods we eat by doing this. For example, tomatoes are sensitive to frost. This shortens their growing season. Fish, on the other hand, survive in very cold water. Scientists identified a particular gene which enables a flounder to resist cold and used the technology of genetic engineering to insert this 'anti-freeze' gene into a tomato. This makes it possible to extend the growing season of the tomato.

enetic engineering, recombinant DNA technology, genetic modification/manipulation (GM) and gene splicing are terms that apply to the direct manipulation of an organism's genes. Genetic engineering is different from traditional breeding, where the organism's genes are manipulated indirectly. Genetic engineering uses the techniques of molecular cloning and transformation to alter the structure and characteristics of genes directly. Genetic engineering techniques have found some successes in numerous applications. Some examples are in improving crop technology, the manufacture of synthetic human insulin through the use of modified bacteria, the manufacture of erythropoietin in hamster ovary cells, and the production of new types of experimental mice such as the oncomouse (cancer mouse) for research.

The term "genetic engineering" was coined in Jack Williamson's science fiction novel Dragon's Island, published in 1951, two years before James Watson and Francis Crick showed that DNA could be the medium of transmission of genetic information.

There are a number of ways through which genetic engineering is accomplished. Essentially, the process has five main steps.

1. Isolation of the genes of interest
2. Insertion of the genes into a transfer vector
3. Transfer of the vector to the organism to be modified
4. Transformation of the cells of the organism
5. Selection of the genetically modified organism (GMO) from those that have not been successfully modified

Isolation is achieved by identifying the gene of interest that the scientist wishes to insert into the organism, usually using existing knowledge of the various functions of genes. DNA information can be obtained from cDNA or gDNA libraries, and amplified using PCR techniques. If necessary, i.e. for insertion of eukaryotic genomic DNA into prokaryotes, further modification may be carried out such as removal of introns or ligating prokaryotic promoters.

Insertion of a gene into a vector such as a plasmid can be done once the gene of interest is isolated. Other vectors can also be used, such as viral vectors, bacterial conjugation, liposomes, or even direct insertion using a gene gun. Restriction enzymes and ligases are of great use in this crucial step if it is being inserted into prokaryotic or viral vectors. Daniel Nathans, Werner Arber and Hamilton Smith received the 1978 Nobel Prize in Physiology or Medicine for their isolation of restriction endonucleases.

Once the vector is obtained, it can be used to transform the target organism. Depending on the vector used, it can be complex or simple. For example, using raw DNA with gene guns is a fairly straightforward process but with low success rates, where the DNA is coated with molecules such as gold and fired directly into a cell. Other more complex methods, such as bacterial transformation or using viruses as vectors have higher success rates.

After transformation, the GMO can be selected from those that have failed to take up the vector in various ways. One method is screening with DNA probes that can stick to the gene of interest that was supposed to have been transplanted. Another is to package genes conferring resistance to certain chemicals such as antibiotics or herbicides into the vector. This chemical is then applied ensuring that only those cells that have taken up the vector will survive.

Applications

The first genetically engineered medicine was synthetic human insulin, approved by the United States Food and Drug Administration in 1982. Another early application of genetic engineering was to create human growth hormone as replacement for a compound that was previously extracted from human cadavers. In 1987 the FDA approved the first genetically engineered vaccine for humans, for hepatitis B. Since these early uses of the technology in medicine, the use of GM has gradually expanded to supply a number of other drugs and vaccines.

One of the best-known applications of genetic engineering is the creation of GMOs for food use (genetically modified foods); such foods resist insect pests, bacterial or fungal infection, resist herbicides to improve yield, have longer freshness than otherwise, or have superior nutritional value.

In materials science, a genetically modified virus has been used to construct a more environmentally friendly lithium-ion battery.

A new type of slowly growing artform is being established via gene engineering and manipulation. Bioart, an artistic form, uses gene engineering to create new art forms that both educate the public about genetics and create living artforms.

During the latter stage stages of the 20th century, man harnessed the power of the atom, and not long after, soon realised the power of genes. Genetic engineering is going to become a very mainstream part of our lives sooner or later, because there are so many possibilities advantages (and disadvantages) involved.

Here are just some of the advantages :

* Disease could be prevented by detecting people/plants/animals that are genetically prone to certain hereditary diseases, and preparing for the inevitable. Also, infectious diseases can be treated by implanting genes that code for antiviral proteins specific to each antigen.
* Animals and plants can be 'tailor made' to show desirable characteristics. Genes could also be manipulated in trees for example, to absorb more CO2 and reduce the threat of global warming.
* Genetic Engineering could increase genetic diversity, and produce more variant alleles which could also be crossed over and implanted into other species. It is possible to alter the genetics of wheat plants to grow insulin for example.



Of course there are two sides to the coin, here are some possible eventualities and disadvantages.

* Nature is an extremely complex inter-related chain consisting of many species linked in the food chain. Some scientists believe that introducing genetically modified genes may have an irreversible effect with consequences yet unknown.
* Genetic engineering borderlines on many moral issues, particularly involving religion, which questions whether man has the right to manipulate the laws and course of nature.

Genetic engineering may be one of the greatest breakthroughs in recent history alongside the discovery of the atom and space flight, however, with the above eventualities and facts above in hand, governments have produced legislation to control what sort of experiments are done involving genetic engineering. In the UK there are strict laws prohibiting any experiments involving the cloning of humans. However, over the years here are some of the experimental 'breakthroughs' made possible by genetic engineering.

* At the Roslin Institute in Scotland, scientists successfully cloned an exact copy of a sheep, named 'Dolly'. This was the first successful cloning of an animal, and most likely the first occurrence of two organisms being genetically identical. Note : Recently the sheep's health has deteriorated detrimentally
* Scientists successfully manipulated the genetic sequence of a rat to grow a human ear on its back. (Unusual, but for the purpose of reproducing human organs for medical purposes)
* Most controversially, and maybe due to more liberal laws, an American scientist is currently conducting tests to clone himself.

Genetic engineering has been impossible until recent times due to the complex and microscopic nature of DNA and its component nucleotides. Through progressive studies, more and more in this area is being made possible, with the above examples only showing some of the potential that genetic engineering shows.

For us to understand chromosomes and DNA more clearly, they can be mapped for future reference. More simplistic organisms such as fruit fly (Drosophila) have been chromosome mapped due to their simplistic nature meaning they will require less genes to operate. At present, a task named the Human Genome Project is mapping the human genome, and should be completed in the next ten years.

The process of genetic engineering involves splicing an area of a chromosome, a gene, that controls a certain characteristic of the body. The enzyme endonuclease is used to split a DNA sequence and split the gene from the rest of the chromosome. For example, this gene may be programmed to produce an antiviral protein. This gene is removed and can be placed into another organism. For example, it can be placed into a bacteria, where it is sealed into the DNA chain using ligase. When the chromosome is once again sealed, the bacteria is now effectively re-programmed to replicate this new antiviral protein. The bacteria can continue to live a healthy life, though genetic engineering and human intervention has actively manipulated what the bacteria actually is. No doubt there are advantages and disadvantages, and this whole subject area will become more prominent over time.




Genetic engineering, more formally known as recombinant DNA technology, allows scientists to pluck genes (segments of DNA) from one type of organism and combine them with genes of a second organism. In this way, relatively simple organisms such as bacteria or yeast, or even mammalian cells in culture and mammals such as goats and sheep, can be induced to make quantities of human proteins, including hormones such as insulin as well as lymphokines and monokines. Microorganisms can also be made to manufacture proteins from infectious agents such as the hepatitis virus or the AIDS virus, for use in vaccines.

Another facet of recombinant DNA technology involves gene therapy: replacing defective or missing genes with normal genes. The first approved gene therapy trials involved children with severe combined immunodeficiency disease, or SCID (Immunodeficiency Diseases), which is caused by lack of an enzyme due to a single abnormal gene. The missing gene is introduced into a harmless virus, then mixed with progenitor cells from the patient's bone marrow. When the virus splices its genes into those of the bone marrow cells, it simultaneously inserts the gene for the missing enzyme. Injected back into the patient, the treated marrow cells produce the missing enzyme and revitalize the immune defenses. Researchers are also investigating the use of gene therapy for such diverse conditions as hemophilia, Parkinson's disease, diabetes, a hereditary form of dangerously high cholesterol, and AIDS.

An increasingly important target for gene therapy is cancer. In pioneering experiments, scientists are removing the immune cell known as the tumor-infiltrating lymphocyte or TIL(Immunity and Cancer), or tumor cells themselves, inserting a gene that boosts the cells' ability to make quantities of a natural anticancer product such as tumor necrosis factor (TNF) or interleukin-2, and then growing the restructured cells in quantity in the laboratory. When the altered cells are returned to the patient, they seek out the tumor and deliver large doses of the anticancer chemical. They also appear to mobilize, in some unknown way, additional antitumor defenses.

On the horizon are anticancer vaccines made by manipulating genes. Intended to protect cancer patients against a recurrence, these vaccines can incorporate genes for immunogenic tumor antigens or genes for histocompatibility antigens able to galvanize killer T cells, as well as genes for substances such as TNF or interleukin-2. Other anticancer strategies call for introducing genes that can shut down cancer-promoting oncogenes or replace faulty cancer-restraining suppressor genes.

Genes can be packaged, for delivery, in a variety of ways: inserted into the genetic material of such carriers as the familiar vaccinia virus (Vaccines Through Biotechnology) or inactivated retroviruses, grafted onto a protein carrier that magnifies the immune response (an adjuvant), or tucked into fat globules known as liposomes.



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Default Genetic Engineering

Introduction: What is Genetic Engineering?

Who would have thought that a tomato could possess characteristics of a fish? What about a plant possessing characteristics of a firefly; or a pig with human traits? These things may sound like science experiments gone wrong, but in truth, these are products of experiments that went well. The fish-like tomato and others are results of genetic modification or genetic manipulation, which are more commonly known as genetic engineering. Genetic engineering is the process of taking genes and segments of DNA from one species and putting them into another species, thus breaking the species barrier and artificially modifying the DNA of various species. These changes in DNA result in an alteration of reproductive and hereditary processes of the organisms since the process is irreversible and the organism's offspring will also possess this unique DNA .


The Process of Genetic Engineering

In order to understand how genetic manipulation is accomplished, it is important first to understand the structure of deoxyribonucleic acid, or DNA. Within its chemical structure, DNA stores the information that determines an organism's hereditary or genetic properties. DNA is made up of a linked series of units called nucleotides , Different nucleotide sequences determine different genes genetic information. Genetic engineering is based on this genetic information.

Genetic manipulation is carried out through a process known as recombinant-DNA formation, or gene splicing. This procedure behind genetic engineering is one whereby segments of genetic material from one organism are transferred to another. The basis of the technique lies in the use of restriction enzymes that split DNA strands wherever certain desired secjuences of nucleotides, or specific genes, occur. This desired segment of DNA is referred to as donor DNA. The process of gene splicing results in a series of fragments of DNA, each of which express the same desired gene that can then combine with plasmids ).

Plasmids are small, circular molecules of DNA that are found in many bacteria. The bacteria act as vectors in the process of genetic engineering. The desired gene cannot be directly inserted into the recipient organism, or host, therefore there must be an organism that can carry the donor DNA into the host. Plasmid DNA is isolated from bacteria and its circular structure is broken by restriction enzymes (Dworkin). The desired donor DNA is then inserted in the plasmid, and the circle is resealed by ligases, which are enzymes that repair breaks in DNA strands. This reconstructed plasmid, which contains an extra gene, can be replaced in the bacteria, where it is cloned, or duplicated, in large numbers. The combined vector and donor DNA fragment constitute the recombinant-DNA molecule. Once inside a host cell, this molecule is replicated along with the host's DNA during cell division. These divisions produce a clone of identical cells, each having a copy of the recombinant-DNA molecule and thus permanently changing the genetic makeup of the host organism ). Genetic engineering has been accomplished.

The Many Uses of Genetic Engineering

Are there any benefits that genetic engineering could bring to humankind? Actually, there are many. By performing genetic engineering, scientists can obtain knowledge about genetic mechanisms. For example, they may be able to uncover some secrets of genetic mapping. Genetic mapping is the identification of individual genes for various functions. If scientists are rising restriction enzymes to splice certain genes, they must be able to identify the genes. Thus, genetic engineering helps to identify certain nucleotide sequences, and to use various restriction enzymes to "read" the sequences. For example, if it appears that a single gene is responsible for a certain function, the recombinant-DNA process may tell us otherwise that two multiple genes, or even other factors are responsible for the specific function .

Genetic manipulation is most commonly used to transfer desirable qualities from one organism to another to improve the ability of other species to serve humankind. Many examples of this lie in the use of genetic engineering to solve many problems with regards to food production and agriculture, waste disposal and industry, as well as disease and medicine . The processes are also used for examining evolutionary processes.

Food Production and Agriculture

Dozens of food crops have now been genetically altered to enhance their qualities for the market or improve growing characteristics. Recombinant-DNA has been used to combat one of the greatest problems in plant food production: the destruction of crops by plant viruses as well as the weather. By transferring the protein-coat gene of the zucchini yellow mosaic virus to squash plants that had previously sustained great damage from the virus, scientists were able to create transgenic squash plants with immunity to this virus .

Scientists have also developed transgenic bacteria that protect strawberry plants from injury by frost. The bacteria commonly found on strawberry plants secrete a protein that initiates the formation of ice crystals when the temperature falls to freezing . In the genetically modified bacteria, the gene that codes for the protein has been deleted. In the absence of the protein, ice formation does not occur until the temperature falls well below the freezing point. Normally, such a deep drop in the temperature does not occur until after the harvest period has ended. The first field test of these genetically modified bacteria was conducted in 1987, on a plot of strawberry plants, and similar experiments on potatoes showed that the gene-spliced bacteria were effective in establishing themselves on the plants and, later in the season, in preventing ice formation during periods of light frost (Levine). Genetic engineering has been used in plants as well as in animals. In the livestock industry, for example, large amounts of a growth hormone found in cows have been obtained from genetically engineered bacteria. When treated with this hormone, dairy cows produce more milk, and beef cattle have leaner meat. Similarly, a genetically engineered pig hormone causes hogs to grow faster and decreases fat content in pork).


Waste Disposal and Industry

Gene transfers also have been applied in the management of industrial wastes. Genetically altered bacteria can be used to decompose many forms of garbage and to break down petroleum products. For example, an 'oil-eating "nonnatural manmade microorganism" exists, and is used for cleaning up oil spills. Recombinant-DNA technology also can be used to monitor the breakdown of pollutants. For example, naphthalene, an environmental pollutant present in artificially manufactured soils, can be broken down by the bacterium Pseudomonas fluorescens. To monitor this process, scientists transferred a lightproducing enzyme called luciferase, found in the bacterium Vibrio fischeri, to the Pseudornonas fluorescens bacterium. The genetically altered Pseudomonas fluorescens bacterium produces light in proportion to the amount of its activity in breaking down the naphthalene, thus providing a way to monitor the efficiency of the process .


Disease and Medicine

Genetic engineering has been used in the field of medicine for many purposes regarding the control and improvement of health. The process has been used to correct inherited genetic defects causing disease (gene therapy), to counter effects of genetic mutations, to produce various pharniaceutical products .

Gene therapy is the use of genetic engineering techniques in the treatment of a genetic disorder or chronic disease. In 1990, a four-year-old girl received genie therapy treatment for adenosine deaminase (ADA) deficiency, an ordinarily fatal inherited disease of the immune system. Because of this genetic defect, the girl was susceptible to recurrent life-threatening infections. Doctors removed white blood cells from the child's body, let the cells grow in the lab, used a genetically modified virus to carry a normal ADA gene into her inimune cells, and then infused the genetically modified blood cells back into the patient's bloodstream. The inserted ADA gene then programmed the cells to produce the missing ADA enzyme, which led to normal immune function iii those cells. This treatment temporarily helped her to develop resistance to infection, and must be repeated periodically .

Another important medical application of the recombinant- DNA procedure has been the production of vaccines against a number of diseases. Heretofore, vaccination against a disease has involved the injection of killed or weakened microorganisms into a person, with the subsequent production of antibodies by the individual's immune system. This procedure has always carried the risk of there being live, virulent pathogens in the vaccine because of some error in the vaccine-producing process (Donnelly).

Through the recombinant-DNA procedure, it is now possible to transfer the genes that stimulate antibody formation to a harmless microorganism and use it as a vaccine against the particular disease. Vaccines have been successfully created using the harmless cowpox virus, the herpes simplex type I virus (cold sores), the influenza virus, and the hepatitis B virus through gene splicing .

Genetic engineering has also contributed several pharmaceutical products (besides vaccinations). Recombinant-DNA procedures involving bacteria and donor DNA fragments have led to the increased availability of such medically important substances as insulin, interferon, and growth hormone (Rubenstein). These substances were previously available only in limited quantities from their primary sources.

Insulin is a hormone produced in the pancreas that controls the absorption of glucose by cells. Diabetics lack the hormone or have decreased levels of it. Using recombinant-DNA techniques, scientists have created human insulin, which is artificially produced by gene-splicing methods in bacteria. Heretofore, diabetic patients relied solely on insulin derived from the pancreases of animals to control glucose levels .

The protein interferon is released into the bloodstream to induce healthy cells to manufacture an enzyme that counters a viral infection. It can also be effective against some forms of cancer, leukemia, genital warts, and the common cold. For many years, the supply of human interferon for research was limited by costly extraction techniques. l-Iowever, the protein became available in greater quantities through genetic engineering .


Evolution

Surprisingly, genetic engineering can also be used to uncover the past. Recombinant-DNA procedures have been used to study the genes of extinct animals. A zebra-like animal called the quagga, for example, became extinct in the '1 9~ century, but some quagga skins with underlying muscle tissues have been salt-preserved in museums. Enzymes were used to release DNA from these muscle cells, yielding DNA fragments representing parts of different genes. These fragments were transferred to the plasmids of bacteria, where they were replicated along with the bacterial DNA. They were then retrieved, analyzed, and compared to corresponding DNA segments of closely related living animals, revealing that the quagga DNA differs from its zebra counterpart by about 5 percent. This amount of difference indicates that the quagga and zebra shared a common ancestor. With appropriate modifications, it should be possible to use this technique to study genes from the bones and teeth of long-extinct animals, providing new insights into the evolutionary process .


The Dangers of Genetic Engineering

Even though it may seem as if genetic engineering has so many positive aspects, there are just as many negatives to counter. Genetic engineering is really a test tube science which may be prematurely applied. A gene studied under a closed system, a test tube with no outside influence on the conditions of the experiment, can only give results about what it does and how it behaves in that particular system. The experiment cannot tell what the role and behavior of donor DNA will be once it's in the host cell, which is likely to be a totally unrelated species that may be very different from the experimental environment . The insertion of a foreign gene might trigger new cellular activities or interrupt current ones. For example, genes can normally be exchanged between different species, but the frequency of these natural transfers is limited by their defense (immune) systems. The immune system serves to prevent invasion by harmful foreign genes, viruses, and other substances, so that particular species is able to maintain its characteristic traits and norma] metabolism . Genetic engineering, may, in turn, disrupt and weaken the immune systems by introducing foreign substances into organisms that they won't be able to fight. No one really knows the overall effect of this .

Foreign genes trigger new cellular activities in the form of resistance. The vectors used in the genetic engineering process are often resistant to many drugs such as antibiotics. Injecting a drug-resisting vector into a new organism will result in a drug-resistant host organism. The resistance may not necessarily be only to drugs, as is the case with frost-resistant plants. Since genetic engineering is irreversible, this method allows these altered organisms to become widespread in nature.

Creating organisms that are resistant to anything they weren't initially unaffected by disturbs the evolutionary process of natural selection, or survival of the fittest. Putting such a desirable gene into an organism may give them an edge over another that would not normally exist. This whole idea of meddling with nature raises a question of religion and ethics (Rubenstein). What about "God;" Do we have the right to be playing the role of a higher being? In fact, genetic engineering raises countless more unanswered questions. Should animals be used in research? Do animals have "rights", as we think of "human rights?" How does genetic engineering of food affect religious and other groups with strong dietary laws, such as vegetarians? How great are the potential risks involved in releasing genetically modified organisms into the biosphere without knowing all the possible consequences?

Other dangers of genetic engineering include the following:

* New toxins and allergens in foods as well as other damaging effects on health caused by unnatural foods: The process of genetic engineering can thus introduce dangerous new allergens and toxins into foods that were previously naturally safe. Already, one genetically engineered soybean was found to cause serious allergic reactions, and bacteria genetically engineered to produce large amounts of the food supplement tryptophan have produced toxic contaminants that have killed 37 people and permanently disabled 1,500 more .
* The disturbance of ecological balance and the spread of diseases across species barriers: When genetic engineers insert a new gene into any organism, there are "position effects" which can lead to unpredictable changes in the pattern of genetic function. The protein product of the inserted gene may carry out unexpected reactions and produce potentially toxic products. There is also serious concern about the dangers of using genetically engineered viruses as vectors in the generation of transgenic plants and animals. This could destabilize the genome, and also possibly create new viruses, and thus dangerous new diseases .
* Unnatural loss of bio-diversity in crops: Biotechnology companies claim that their manipulations are similar to natural genetic changes or traditional breeding techniques. However, the cross-species transfers being made, such as between fish and tomatoes, or between other unrelated species, would not happen in nature and may create new toxins, diseases and weaknesses (Rubenstein). Also consider the fact that organisms are "sharing" characteristics that are supposed to be unique to them. , For example in the fish-like tomato, a fish and a tomato are no longer unique. There is less diversity since they are now more similar, though unnaturally, than they initially were.
* The creation of herbicide-resistant weeds, resulting in increased pollution of food and water supply: More than 50% of the crops developed by biotechnology companies have been engineered to be resistant to herbicides. Use of herbicide-resistant crops will lead to a threefold increase in the use of herbicides, resulting in even greater pollution of our food and water with toxins.
* Unexpected characteristics may appear in genetically altered organisms:One batch of genetically engineered young salmon were pale green instead of the normal brown color of young salmon and rather than turning pink on maturation, they remained green.
* Artificially induced characteristics and inevitable side effects will be passed on to all subsequent generations and to other related organisms. Once released, they can never be recalled or contained. The consequences of this are incalculable ). Even when genetically engineered fish have appeared normal, their descendants have been born with deformities such as grotesquely deformed heads and gill flaps, and change of color .


Regulation of Genetic Engineering

Although numerous dangers of genetic engineering exist, they have been highly exaggerated. There is a great need to understand the genetic basis of all diseases, not just those to be errors of experiments. For genetic diseases, the solution lies in curing the defects rather than in managing with lifelong and often inadequate treatments. Vaccines have been developed through genetic engineering and have virtually eliminated some of mans most dreaded diseases. Even though vaccines do kill or maim a small number of those inoculated, the exaggeration of the downsides and possible dangers in these experiments diverts attention from the research needed to solve these problems and prevent others . The potential dangers of such research must be balanced against the actual tragedies caused by other sources.

In an effort to prevent worldwide epidemics and other problems as a result of genetic engineering, the National Institutes of Health (NIH) has established regulations, and has published safety guidelines to minimize the hazards of research . These guidelines have been gradually relaxed because such research was proven to be safe. In 1985, the NIH approved experimental guidelines for treatment in which genes are transplanted to correct hereditary defects in human beings (gene therapy). In 1987, a committee of the National Academy of Sciences concluded that transferring genes between species of organisms posed no serious environmental hazards ).


Conclusion

Genetic engineering is a complicated process that can be used for many things from modifying organisms such as plants to serve humankind better, to developing helpful pharmaceutical products, and even providing clues to the evolutionary process . Despite the fact that the genetic manipulation process seems to result in more damage than help, these views are often exaggerated. Although no one can predict the future of any field of human endeavor, genetic engineering appears to be a feasible mechanism through which many problems of modern society can be solved.

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well! ur contribution is marvellous and ofcourse valuable.
i want to know from where r u getting these compact details/ do u have some authentic websites or you have your own notes to share?
it will be very kind of you if u mention the sources especially the books and websites.
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Originally Posted by prissygirl View Post
well! ur contribution is marvellous and ofcourse valuable.
i want to know from where r u getting these compact details/ do u have some authentic websites or you have your own notes to share?
it will be very kind of you if u mention the sources especially the books and websites.
regards
Thanks dear.
These are not my notes i never had the time to make my own notes.I have searched these notes from different websites some to mention are

Encarta
Britannica
Tutor Vista
Answer.com
Wikipedia
Wikianswers
and many more.

Diagrams are randomly selected illustrations
some of the presentations are from scibd.
Books i have mentioned in the relevant section.
I will try to add a reference next time in the notes.

You must search your own notes and follow the books as well.These are just reference material for those candidates who find zoology difficult to cover.I hope the notes are of some help to the zoology candidates.
Regards.
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