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future use of the human genome project
future use of the human genome project
significance of the human genome project
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The Human Genome Project
Begun formally in 1990, the U.S. Human Genome Project is a 13-year
effort coordinated by the U.S. Department of Energy and the National
Institutes of Health. The project originally was planned to last 15
years, but rapid technological advances have accelerated the expected
completion date to 2003. Project goals are to
* identify all the approximate 30,000 genes in human DNA,
* determine the sequences of the 3 billion chemical base pairs that
make up human DNA,
* store this information in databases,
* improve tools for data analysis,
* transfer related technologies to the private sector, and
* address the ethical, legal, and social issues (ELSI) that may
arise from the project.
To help achieve these goals, researchers also are studying the genetic
makeup of several nonhuman organisms. These include the common human
gut bacterium Escherichia coli, the fruit fly, and the laboratory
mouse.
Why do the Human Genome Project?
--------------------------------
Most inherited diseases are rare, but taken together, the more than
3,000 disorders known to result from single altered genes rob millions
of healthy and productive lives. Today, little can be done to treat,
let alone cure, most of these diseases. But having a gene in hand
allows scientists to study its structure and characterize the
molecular alterations, or mutations, that result in disease. Progress
in understanding the causes of cancer, for example, has taken a leap
forward by the recent discovery of cancer genes. The goal of the Human
Genome Project is to provide scientists with powerful new tools to
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... a definitive sequence creates
uncertainty about the appropriate definition of "normal," which in
turn makes the discussion of public policy issues difficult. Questions
about controlling the manipulation of human genetic materials concerns
these critics, as does the idea that simply because these scientists
are able to do this science, they ought to. These critics point to the
development of atomic weapons and argue that the science that led to
their development caused far more problems than it resolved.
Few religious groups in the United States formally have addressed the
specific ethical and public policy issues raised by the HGP, although
there is active interdenominational discussion of issues related to
human genetics in general. Public policy debates are enriched
considerably by input from these various groups.
The more we know about genetics and the building blocks of life the closer we get to being capable of cloning a human. The study of chromosomes and DNA strains has been going on for years. In 1990, the Unites States Government founded the Human Genome Project (HGP). This program was to research and study the estimated 80,000 human genes and determine the sequences of 3 billion DNA molecules. Knowing and being able to examine each sequence could change how humans respond to diseases, viruses, and toxins common to everyday life. With the technology of today the HGP expects to have a blueprint of all human DNA sequences by the spring of 2000. This accomplishment, even though not cloning, presents other new issues for individuals and society. For this reason the Ethical, Legal, and Social Implications (ELSI) was brought in to identify and address these issues. They operate to secure the individuals rights to those who contribute DNA samples for studies. The ELSI, being the biggest bioethics program, has to decide on important factors when an individual’s personal DNA is calculated. Such factors would include; who would have access to the information, who controls and protects the information and when to use it? Along with these concerns, the ESLI tries to prepare for the estimated impacts that genetic advances could be responsible for in the near future. The availability of such information is becoming to broad and one needs to be concerned where society is going with it.
The debate over the importance of a Human Genome Project can be cleared up by looking at what the human genome actually is, and why knowing its DNA sequence can be beneficial to the scientific and the human community. The human genome is made up of about three billion base pairs, which contain about 100,000 genes. The 100,000 genes in the 46 human chromosomes only account for a small total of the DNA in our genome. Approximately 10 percent of our DNA make up these genes in our genome, these genes are what is actually encoded for and used by our body to make vital proteins needed for everyday life. The remaining 90 percent of our three billion base pairs are repeated sequences between genes that do not encode for any particular product. These repeated sequences account for the reason why 99 percent of any humans DNA is identical to another human's (1). With this knowledge many people believe it is not worth the time or money to sequence the entire human genome when only a small percent is used to encode for proteins. However, by sequencing the whole genome researchers will no longer have to do a needle in the haystack type of search for small genes, like the one found on chromosome four that is responsible for Huntington's disease (4). Also, knowing the complete human DNA sequence will allow scientists to determine the role and importance of the repeated DNA, non-protein encoding, sequences in our body.
Kevles, Daniel J. and Leroy Hood. "Will the Human Genome Project Lead to Abuses In Genetic Engineering?" Taking Sides. Ed. Thomas A. Easton. Guilford, Connecticut: Dushkin Publishing Group Inc., 1995. 342-357.
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...
The purpose of the human genome project was to select the best pairs of the genes and the desirable characteristics in the human beings to maintain the production of the organisms according to the desirable gene sequencing. This project was initiated to control the sequencing of the gene artificially [1]. The world’s largest biological plan was the human genome project as it was started on the large scale. The idea of this project was given by the researchers in 1984. The practical work started in 1990 to execute the project. The official declaration of the project carried out in 2003. The financial assistance was awarded to the program setup through the healthcare workplaces, where their engagement was significant. Another program
In 1989, molecular biologist Norton Zinder said,”Today we begin” (Begley 56). With these words, Zinder and the National Institutes of Health (NIH), formally launched a monumental effort that could rival in scope both the Manhattan Project, witch created the A-bomb, and the Apollo moon-landing program-and may exceed them in importance (Jaroff95). The Program will map the human and spell out for the world the entire message hidden in its chemical code. Robert Sinsheimer of the University of California at Santa Barbara says,”The human gene is the complete set of instructions for making a human being “(Begley57). The achievement of the project would launch a new era in medicine. They would be able to predict an individual vulnerability and could eventually develop new drugs to treat or even prevent them. Though they may not have known, thi...
The genetic technology revolution has proved to be both a blessing and a blight. The Human Genome Project is aimed at mapping and sequencing the entire human genome. DNA chips are loaded with information about human genes. The chip reveals specific information about the individuals’ health and genetic makeup (Richmond & Germov 2009).The technology has been described as a milestone by many in that it facilitates research, screening, and treatment of genetic conditions. However, there have been fears that the technology permits a reduction in privacy when the information is disclosed. Many argue that genetic information can also be used unfairly to discriminate against or stigmatize individuals (Willis 2009).
Can you imagine knowing your own genetic code? Going into the doctor for a routine physical and leaving with the knowledge of your genetic downfalls so that you may prevent disease and cancers. This may seem unbelievable but it is likely to be implemented in the near future. Since the start of the human genome project, the medical community has been anxiously awaiting its completion because the applications it has to this field are obviously enormous. However, we still have much to learn about genetic variability and the information we gain can be used to prevent, repair, and eradicate illness.
So what is a human genome and why is the government researching it? The Human genome is the sequence of roughly 20,000 genes that make up human Deoxyribonucleic acid (DNA), or the building blocks that tell cells what to do. The government project named Human Genome Project (HGP) started in 1990’s, and is trying to unravel the 3 billion chemical base pairs in a DNA strand (http://www.ama-assn.org/ama/pub/physician-resources/medical-science/genetics-molecular-medicine/current-topics/human-genome.shtml.)
For numerous years, the world’s most prestigious geneticists have been trying to crack the human genetic code, the intricate puzzle that defines each and every one of us as individuals. With the monumental success of the Human Genome Project, a new and exciting biological frontier is ready for exploration. The ramifications of the knowledge derived from this endeavor will no doubt be staggering for residents of the Rio Grande Valley and the world at large.
Is it possible to eradicate disease entirely? A half-century ago, little was known about how disease was affected by genetics. In 1953, James Watson and Francis Crick discovered the double helix structure of DNA. In the mid 1970’s, ways were developed to determine the order, or sequence, of the chemical letters in DNA. The Human Genome was completely unknown to man until 1990, when the National Institutes of Health (NIH) and the Department of Energy teamed up with international partners to complete the entire 3 billion base pairs of the Human Genome. The goal of this project was to understand the genetic factors in human disease and to hopefully find ways to diagnose, treat, and prevent disease. The Human Genome project has supported an Ethical, Legal and Social research program to address the many issues that might arise from this study. The Human Genome Project should continue because it has the potential to unlock the cure to countless diseases.
Research projects such as the Human Genome Project (a government-funded program to map the estimated 100,000 genes that make up the human species) provide a valuable resource in the search for treatments and cures of genetic disorders. 400 of the 2000 genes studied have already been linked to genetic disorders.
Current technology has made what once seemed impossible, mapping the human genome, a reality within the next decade. What began over forty years ago with the discovery of the basic structure of DNA has evolved into the Human Genome Project. This is a fifteen-year, three billion dollar effort to sequence the entire human genetic code. The Project, under the direction of the U.S. National Institute of Health and the department of Energy is ahead of schedule in mapping what makes up an individual's genetic imprint. Much of the current efforts in genetic engineering have been focused on genes that cause disease and to date, about eight hundred and eighty of these "disease" genes have been found. They include genes for Huntington's disease, cystic fibrosis, schizophrenia, Alzheimer's, Duchenne muscular dystrophy, familial colon cancer, breast cancer and many more. Once the human genome is mapped, the next logical step is gene therapy, in which a missing gene is added or a defective one is removed.
The Human Genome Project is the key behind any advancement in genetic therapy. The goal behind this project is to identify all of the human genes and successfully map and sequence the human genome. This research is very significant because the data found in this research will be used to find and possibly cure genetic disorders. More than five thousand monogenic disorders have been found in humans. Many of which do not have a sure-fire cure at the present time. Thus information gathered through the efforts of the Human Genome Project is essential in order to derive gene-altering cures for genetic disorders.
This is the outstanding achievement not only of our lifetime, but of human history. I say this, because the Human Genome Project has the potential to impact the life of every person on this planet. It is a giant resource that will change mankind, much like the printing press did.