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Genetics

Just because scientists did not know exactly how heredity and genetics worked did not stop people from using what they observed. People have been manipulating the phenotypes of plants and animals for centuries. This practice is called selective breeding.

genetics

Farmers, for example, might selectively breed plants that are more resistant to disease or that yield a larger crop. Dairy farmers might selectively breed dairy cows that routinely produce more milk. Poultry farmers might selectively breed hens that lay the most eggs. If a dairy farmer crosses a cow that produces a lot of milk with a bull that comes from a line of long-lived cattle, the resulting offspring could carry both of these advantageous traits. The offspring is called a hybrid. Animal and plant hybrids are produced by crossing parents that are genetically different.

If this selective breeding goes on from generation to generation, there is a danger of losing genetic diversity. Genetic diversity is important because it allows organisms to adapt to adverse conditions such as a lack of food or outbreaks of disease. When animals or plants that have a desired trait are bred with another that has the same trait, other genes (the ones that do not code for the advantageous trait being selected for, but may code for other important traits) are in danger of getting permanently lost. This is called in-breeding depression. For this reason, breeders try very carefully to produce animals and plants that are heterozygous, in order to preserve genetic diversity.


Early Ideas about Heredity

People have always been interested in how a child comes to look like other members of its family. However, scientists did not discover DNA, genes and chromosomes until relatively recently. But that did not stop people in earlier times from taking a guess about how heredity works. For the most part, their beliefs came from interpretations of what they saw. In other words, their conclusions were not tested using the scientific method; they were based only on untested observations.
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Gregor Mendel: The Father of Modern Genetics

Gregor Mendel (1822–1884) is often called the “father of heredity.” Mendel was a monk and a high school physics, mathematics, and Greek teacher, but he was also one of the first genetics researchers. Most of Mendel’s research was carried out in the Czechoslovakian monastery where he lived. He experimented with the way traits are passed from generation to generation in pea plants by researching seven main characteristics: flower color, flower position, stem length, pod shape, pod color, seed shape, and seed color.
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Chromosome Theory of Heredity

In the early 1900s, Thomas Hunt Morgan (1866–1945), a biologist who studied fruit flies, was about to make his contribution to the science of genetics. The scientific name for the common fruit fly is Drosophila melanogaster (D. melanogaster). Morgan found that when he crossed a red-eyed female fly with a white-eyed male fly, all of their offspring had red eyes. But when he took some of these red-eyed offspring and crossed them with their siblings, the white-eyed trait reappeared in the offspring. Morgan noticed that all of these white-eyed F2 generation flies had something in common—they were all male. From the results of his experiments, Morgan determined that eye color in the fruit fly is linked specifically to the X chromosome.
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Passing Genes to the Next Generation

Following the discovery of the structure of DNA, scientists knew that the DNA molecule carried hereditary information from one generation to the next and what the molecule looked like. But exactly how do cells use the DNA molecule?
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Down Syndrome - Nondisjunction During Meiosis

Most of the time, meiosis goes normally. But, occasionally, things do not go quite as they are supposed to. Down syndrome, for example, is a genetic disorder that is caused by an error in meiosis. The error results when a gamete, usually an egg, has two copies of chromosome 21 instead of one copy. When a normal gamete joins with a gamete that contains two of chromosome 21, the resulting fertilized egg contains three of chromosome 21. This is the reason that Down syndrome is also called trisomy 21. At the age of 25, women have about a 1 in 1,300 chance of having a baby with Down syndrome. That risk increases to 1 in 365 by the time the woman turns 35, and then 1 in 30 by age 45 because as she gets older, the chance of meiosis going wrong increases.
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Genetic Technology

While CML is not an inherited disease, scientists hope to one day use the same concept to treat or cure genetic diseases. One step in that process was the Human Genome Project, which could give scientists the tools they need to change the future of genetic research.
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Genetic Testing

Geneticists have not only identified genes that cause genetic disease, but they have also developed genetic tests to detect these diseases as well as researched possible cures for them.
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Inherited Conditions

A mistake during meiosis affects the way a gamete is formed. If abnormal gametes are a product of nondisjunction, the chance of the same parents having another child with the same disorder is minimal. However, if abnormal gametes are produced due to a balanced translocation, the chance of having another similarly affected child increases. A mistake during meiosis is only one way damaged DNA can be inherited by an offspring. Sometimes parents can carry a damaged gene that has been passed down to them through generations. Many times they are not aware they carry the gene until they have an affected child.
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Genetic Mutations and Cancer

All cancers are caused by a change in DNA, but most cancers are not hereditary. If genetic mutations occur that damage the way cells regulate their growth and death, cancer can be the result. Oncogenes are mutated genes that convert normal cells into cancerous cells. Before they are mutated, oncogenes are called proto-oncogenes. Proto-oncogenes are normal genes that carry the information that tells a cell when to divide. When a proto-oncogene mutates into an oncogene, cells can grow out of control.
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Other Chromosomal Abnormalities

Most of the time, the correct number of chromosomes develops in a fetus. However, just because a fetus has the correct number of chromosomes does not necessarily mean that all of those chromosomes are intact.
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