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Human Genome Project

The Human Genome Project (HGP) is an international research effort to decipher the entire human genome and understand the unique hereditary instructions that each person possesses. The HGP is a jointly funded project by the U.S. Department of Energy (DOE) and the National Institutes of Health (NIH) with additional research done by the National (NHGRI). The project, launched in 1990, was originally planned to last 15 years, but rapid advances in technology have accelerated the expected completion date to 2003. The Joint Genome Institute (JGI), established in 1997, is one of the largest publicly funded human genome sequencing centers in the world and contributes greatly to the HGP. The Wellcome Trust in the United Kingdom also contributes substantial investments to the HGP.

The roots of the HGP can be traced back to the atomic bomb era that began during World War II. Descendants of bomb survivors harbor DNA mutations as a result of severe radiation exposure. These mutations were passed to their descendents who developed horrible diseases and malformations. The DOE’s role in the HGP arose to study the genetic and health effects or potential health risks of radiation and chemical by-products of energy production. Scientist


Damaged or mutated DNA are heritable changes that may result from uncorrected errors in replication, failure to repair damage correctly, or from spontaneous rearrangements. A mutation is a permanent change in the bases that make up a gene. Since the bases constitute the code letters, which direct what amino acids are incorporated in to a protein, changes in the bases of DNA often result in substantial changes of protein function.

While mapping chromosomes, scientists use markers to locate different genes. To figure out what chromosome the gene is on, probes highlight the chromosome and the general location of the gene. Then, scientists cut out pieces of the chromosome with special enzymes. With these pieces, scientists clone hundreds of copies of these fragments and sequence the DNA to find recognizable DNA markers and look for places where the fragments share some of the same markers. When researchers wish to sequence a fragment, they run four nearly identical reactions using that DNA as a template, in which the four bases are labeled with different fluorescent dyes.

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Approximate Word count = 2575
Approximate Pages = 10 (250 words per page double spaced)


  

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