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Essay on human genome project
The significance of the human genome project
Importance of the human genome project
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Ari Patrinos and Francis Collins combined forces in order to make the completion of the Human Genome Project possible with the fifteen year time frame. Ari Patrinos supervised the United States Department of Energy’s Human Genome Research. Francis Collins regulated the National Institute of Health National Human Genome Research Institute.
Besides the United States Department of Energy and the National Institute of Health, several universities across the United States were involved in the Project, along with various other countries. Although numerous other countries contributed to the global Project, research in the United Kingdom, China, France, Japan, and Germany played a more significant role.
In 1953, three significant people in modern genetics made a great discovery. With the finding of DNA’s double helix structure, researchers were now able to fully understand DNA. DNA’s double helix structure allowed other life sciences to be further explored. This structure was discovered by James Watson, Francis Crick, Rosalind Franklin and Maurice Wilkins.
The Sanger Centre in the United Kingdom contributed greatly to the human genome project. Thirty three percent of the work in progress genome was produced by the Centre. The other sixty percent was to be produced by the universities and research labs involved in the Project in the United States. While ninety percent of the still developing outline human genome was to be released by the year 2000, the outline was not officially published until February of 2001.
After discovering the location of three significant disease genes, Francis Collins became director of the National Institute of Health. These disease genes include those accountable for: Huntington’s disease, cystic fibro...
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...articular disease and design a prevention strategy for that disease.
Although much of pharmacogenetics is still in research, the genome sequence has encouraged the current practice in medicine. For example, HIV-positive individuals are tested to clarify vulnerability to the antiretroviral drug Abacabir. Abacabir reduces the quantity of HIV in the blood and the patient’s likelihood of acquiring AIDS. Another example of the use of pharmacogenetics in medicine is the testing of individuals to ascertain the genetic alteration of thiopurine S-methyltransferase, or TPMT. The recommended dosage of azathioprine, which is used to improve severe rheumatoid arthritis, is determined by the patient’s TPMT genetic variation. If unconverted azathioprine fabricates in the bone marrow, it can eradicate maturing white blood cells and can leave a patient susceptible to infection.
In 1990, the first great stride of genetics took place. This was called the Human Genome Project, a large-scale operation that was designed to understand the human genome (genetic structure). Since its commencement, there have been many leaps and bounds that have taken place. For certain genetic issues that we once knew nothing about, we no...
These discoveries about the structure of DNA allowed scientists to explore the genome and develop a stronger understanding of genes. Within a decade of its discovery, other scientists had identified the genes responsible for specific diseases and traits. The discovery of the structure of DNA created a basis for ...
If Nathaniel Wu did not have the allele for Huntington’s disease, he would undeniably be the perfect scientist for the position in the eyes of the IPC. Wu is a 30-year-old microbiologist at one if the best research laboratories worldwide. After a series of interviews, the IPC was convinced his determination was not only factor that qualified him more in comparison to the other candidates; they realized that his potential “[is] likely to result in the type of discoveries for new drugs and treatments,” a goal that has not been reached since Dr. Peters’s incident. Wu is also known as a creative researcher and a hard worker, meaning that hiring him will likely result in a dramatic increase of earnings for the IPC. Considering that Huntington’s disease will most likely deteriorate Wu’s abilities, many may argue that it is not worthwhile to hire Wu; it is foreseen that the symptoms of Huntington’s disease begin to appear as soon as th...
Francis S. Collins is a renowned geneticist who originally became Ph.D in Physical Chemistry at Yale University and later on, a Medical Doctor at University of North Carolina. As soon as he graduated he was offered a fellowship in Human Genetics at Yale University under the guidance of Sherman Weissman, currently Sterling Professor of Genetics. In the late 1980’s Collins became known in the field of Medical Genetics for his development of positional cloning, a technique that allows to locate a hereditary disease-causing gene by studying the inheritance pattern within a family. Working with his method researchers found the genes responsible for diseases like Cystic fibrosis, Huntington’s disease, Neurofibromatosis, Multiple Endocrine Neoplasia type one, and Hutchinson-Gilford Progeria Syndrome. In 1993 Dr. Collins succeeded Dr. James D. Watson as the director of the National Human Genome Research Institute (NHGRI), overseeing the role of the United States in the mapping of the human genome. In 2009 President Obama personally recommended Collins to lead the National Institute of Health (NIH) where he works until present day. Francis S. Collins is by no means a bragging individual, bits and pieces of his accomplishments are scattered throughout the book and he makes no big deal about it; instead he j...
Huntington's disease is a progressive brain disorder that is caused by a single defective gene on chromosome 4 — which is one of the 23 human chromosomes that carry a person’s entire genetic code (alz.org, 2013). This defect is dominant, w...
James D. Watson is a molecular biologist, geneticist and zoologist. He is well known as one of the two men who discovered DNA. The other man who helped discover DNA is Francis Crick. Francis is a biologist, neurologist and a biophysicist.
This book is about the amazing task of mapping and showing all the sequences of the thousands and thousands of genes in the human body. The book is split up into nine chapters each of which covers a different aspect of this incredible project. The book tells all about almost every aspect of the project. It tells all about the project and what the point is, what has been accomplished so far, and when they expect it to be finished. According to the introduction the project is actually expected to be finished sometime this year.
About fifteen years ago at a conference near Salt Lake City, the Department of Energy brought up a question that would change the face of science, more specifically molecular genetics. They questioned why there was no DNA research on the way mutations are detected and they decided to change that. Thus, the Human Genome Project was born. Actually there was a lot more planning to do before the work began, ranging from the technical aspects to developing a separate commission dealing with the ethical issues. Eight years after officially starting the project, the public is in awe of what has been accomplished. The projected goal is to have an accurate, complete sequence of human DNA by the year 2003, two years sooner than previously expected (Collins, 1998). The reason for the project is on schedule is that innovative techniques are being applied in DNA sequencing that are more cost effective as well as more efficient.
heated in the recent years. Following the mapping of the human genome, scientists are pursuing
The use of genetic sequencing in the medical field has innumerable possibilities; genomic medicine, as this new field is now called, will enable the human race to make immense advances in understanding how our genetic heredity makes us susceptible to some illnesses and immune to others. The detection of diseases with a high rate of heredity is just one facet of the gem that is genomics; once researchers are able to map out all of the vital components and rare alleles that sometimes play a large factor in disease, it will be possible to target these specific gene combinations, functional elements, and alleles. Because of the fact that protein, produced by our cells’ ribosomes, has an effect on the pathways that help express our inherited traits, it is important that we understand the relationship between DNA and protein, and how this affects the phenotype of an individual’s genetic attributes. For example, sickle-cell anemia is caused by a flaw in one nitrogenous base sequence in DNA. This flaw then translates into RNA, then into amino acids that determine the phenotype that the subject will have. The discrepancy in something as minute as a nitrogenous base and one amino acid makes the difference between a healthy, normal life and a life ...
In April 2003, researchers successfully completed the Human Genome Project, more than two years ahead of schedule. The Human Genome Project has already led to the discovery of more than 1,800 genes that cause disease (“NIH Fact Sheets…”). As a result of the Human Genome Project, researchers can find a gene suspected of causing an inherited disease in a matter of days, rather than the years it would have taken before. “One major step was the development of the HapMap. The HapMap is a catalog of common genetic differences in the human genome. The HapMap has accelerated the search for genes that have a say in common human disease, and have already produced results in finding genetic factors involved in conditions ranging from age-related blindness to obesity”(NIH Fact Sheet). The Can...
"The discovery of the structure by Crick and Watson, with all its biological implications, has been one of the major scientific events of this century." (Bragg, The Double Helix, p1) In the story of The Double Helix, James Watson tells of the road that led to the discovery of life's basic building block-DNA. This autobiography gives insight into science and the workings within a professional research laboratory that few members of society will ever be able to experience. It also gives the reader an idea of the reality of life for one scientist and how he struggled with the problem of DNA. However, the author's style is marked by his lack of objectivity and inclusion of many biased opinions and personal prejudices.
The Double Helix tells a tale of fierce competition, perseverance, and scientific innovation as we follow James Watson and his cohort Francis Crick on their quest to discover the secret to life, the structure of deoxyribonucleic acid. Although already fascinated with DNA, Watson struggled with finding chemistry exciting enough to learn it in depth. He had studied birds in college and thereby managed to avoid any formal chemistry or physics courses. As he later pursued a PhD in biochemistry, he realized he could put it off no longer and attempted to learn organic chemistry at Indiana University. However, after a mishap in the lab, he was encouraged instead to study nucleic acid chemistry with Herman Kalckar in Copenhagen. There, his mind strayed from his work and he began doing unauthorized research in the lab of Ole Maaløe, studying phages. Herman stopped teaching Watson after going through a divorce with his wife, and sent Watson off to a scientific conference in Naples. Although he was bored by many of the lectures, Maurice Wilkins’s talk about X-ray diffraction fascinated Watson. He was struck by an X-ray diffraction picture of DNA that Maurice presented and was determined to study the acid. He later got to know more about Maurice’s colleague, Rosalind Franklin, who was proud, stubborn, and very difficult to work with. Watson greatly admired the lecture given by the renowned Linus Pauling, who had discovered the structure of the alpha-helix and was thought of as the leader in DNA research in the scientific world.
The scientific and medical progress of DNA as been emense, from involving the identification of our genes that trigger major diseases or the creation and manufacture of drugs to treat these diseases. DNA has many significant uses to society, health and culture of today. One important area of DNA research is that used for genetic and medical research. Our abi...
...f the structure of DNA by James Watson and Francis Crick in 1953 that was extremely influential for future researchers. They determined that DNA was a double helix structure composed of base pairings, with a sugar phosphate backbone. This model explained how “genes can duplicate themselves [and] would eventually lead to our current understanding of many things, from genetic disease to genetic engineering” (Salem).