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Ethical issues in genetic research
Essays on the human genome project
Ethical issues in genetic research
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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.)
DNA is made up of phosphates, sugars and amino acids, Adenine (A), Thymine (T), Cytosine(C) and Guanine (G). Each amino acid is paired with its opposite, A is always paired with T and C with G. These pairing in a specific order make codes that cells use as instruction for making proteins that perform specific functions in cells. The purpose of the HGP is to identify all genes in human DNA, store the information in a database, while improving the tools used to sequence DNA (Toriello, pg 15-28.) The project also has to deal with the ethical issues that come from these experiments. In 2003 after 13 years a full strand of DNA was decoded. Of course each person’s DNA is unique, with the exceptions of identical twin, so much more work is yet to be done to make this technology useful in every day life.
Once a DNA strand is sequenced there are many ways to use the information found in it. One possibility is to find what genes influence the development of diseases, like cancer, deformities, or Alzheimer’s, only to mention a few. If you know you have the gene on chromosome 19 that is linked with Alzheimer’s, there may be ways to treat the disorder early, slow its progress, or even prevent it. At the very least the family can prepare for th...
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Works Cited
Puck, Jennifer, Malech, and Harry. National Human Genome Research institute, Genetics and Molecular Biology Branch. Jan 31, 2006. Jan 1, 2010. https://www.123HelpMe.com/view.asp?id=154080.
Human Genome. 1995. American Medical Association. Jan 1, 2010. http://www.ama-assn.org/ama/pub/physician-resources/medical-science/genetics-molecular-medicine/current-topics/human-genome.shtml
Carroll, Sean. The making of the fittest. New York: Julia Druskin, 2006.
Nicolson, Cynthia. Baa. Toronto: Kids Can Press Ltd, 2001.
Gralla, Jay. Understanding Cloning. Indianapolis: Marie Butler-Knight, 2004.
Walker, Richard. Genes & DNA. Boston: Kingfisher, 2003.
Toriello, James. The Human Genome Project. New York: Rosen Publishing Group, 2003.
Fridell, Ron. Genetic Engineering. Minneapolis: Lerner Publications Company, 2006.
It helps medics to find a direct genetic cause of the patient’s condition and target it with pharmaceutical or other therapies. The technology is used for the identification of DNA sequences that increase risks of current diseases and disorders; with this information carriers can start to make efforts to prevent them before the development of the problem. The video mentioned 200 actionable genes, structures that have direct links with a specific condition. Knowing about their presence, people have a chance to bring in preventive measures like taking anticoagulants in the case of identification of a thrombogenic gene. The technology led to the significant improvement of diagnostics and personalized treatments. It helped to find a rare, life-threatening mutation in case of Beery twins and assign a drug to a girl (Alexis) that returned her to a normal life. In the case of cancer genome sequencing led to the development of genetic drags, which target essential tumor genes and make malign structures to shrink. The video mentioned a product that works with the BRАF protein that induces cells to uncontrolled division; the drug led to the remission in the patient with metastasizing melanoma. Such treatment was effective in the case of cystic fibrosis. In the case of the breast cancer the technology helps to evaluate the aggressiveness of the condition and make a personalized decision about chemotherapy. The video also mentioned the pre-implantation genetic diagnosis – an early-staged technology that prevents the development of inherited disorders in
Miller, K. R., & Levine, J. S. (2010). Miller & Levine biology. Boston, Mass: Pearson
Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/22441230.
Miller, K. R., & Levine, J. S. (2010). Miller & Levine biology. Boston, Mass.: Pearson.
-Reilly Philip. Is It In Your Genes. Cold Spring Harbor Laboratory Press. 2004: 223-228. Print
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.
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 ...
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 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).
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 ...
The Human Genome Project is essential for the human race to advance. With the ability to decimate human disease and even boost food resources, people will increase life expectancy alongside decreasing the percent of people around the world who go hungry each day. There can even be limits placed on Legal aspects of The Human Genome Project results that appease civil rights activists and will preserve ethics and diversity while still improving mankind. Humans will never have to fear disease or hunger. The future looks bright for all of mankind.
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...
For example such as medicine, it can be sometime possible to reading DNA sequences and find out how some diseases occur. It can sometimes be possible to fight some infectious diseases or any form of disease by changing the DNA codons which cause most of these problems.
Web. The Web. The Web. 04 Dec. 2013. http://www.ncbi.nlm.nih.gov/pubmed/21663987
23andMe, a web-based service that helps customer read and understand their DNA, is an extremely determined firm in the genomic industry with its mission, “To help people access, understand and benefit from the human genome.” (Our mission). The culture of 23andMe was built on its six fundamental values and beliefs. First, “Think big” in terms of utilizing genetic data to modernize health, wellness, and scientific study. Second, “We love DNA” as study of DNA uncovers the secret behind the remarkable human diversity globally.