Transgenics 1

Total Page:16

File Type:pdf, Size:1020Kb

Transgenics 1 Running Head: TRANSGENICS 1 Transgenics: The Scientific Mystery of Today’s Species Leanna B. Rippey Radford University: Core 201 Running Head: TRANSGENICS 2 Abstract Transgenic animals are species that exhibit traits not normally found in an animal. The organism is genetically engineered by removing certain genes and modifying them to function differently in another species. There are many pros and cons to transgenic research. The genes can produce a stronger organism, more capable of producing the goods desired. Transgenics are not organisms being altered through selective breeding, but through technological methods. These technological methods of breeding organisms produces new life forms that sometimes cross species boundaries, and that have long term effects on the environment. Also, the blending of DNA from different organisms may cause unintended personal, social, and cultural consequences. The genes are not normally found in the organism and can produce mass changes. This paper argues that present genetic engineering of species through transgenic research is ethically wrong due to the lack of information given to the general public, causing the De Minimis Dilemma, which states that individuals hold different views of safety. Transgenic research does not typically give the necessary information to develop an opinion of the safety features that the animals are guaranteed in the experiments. Running Head: TRANSGENICS 3 Transgenic research was first recognized as a possibility when DNA was discovered and scientists realized that you could use DNA to construct bacteria and other genes through genetic engineering practices. James Watson and Francis Crick discovered DNA in 1953, which developed transgenic research in the 1950s with Joshua Lederberg. Lederberg pioneered the earliest transgenic techniques by beginning genetic engineering with the shuffling of genetic materials with bacteria (Whitesides, 2003, pp. 529-530). Legerberg was the first to use transgenic research to produce a different gene that could modify another organism in a desired way. Transgenics is the ability to introduce foreign or genetically modified genes into the gene line of an organism and let the genes encounter genetic manipulation (Jaenisch, 1988, p. 1468). Transgenic cells have the ability to pass on the new characteristics to new cells when they reproduce because the organism will reproduce the foreign transgenes during cell division (World of Micrbiology and Immunology, 2003, p. 551). The gene that was genetically modified will be produced for future generations when the organism reproduces because cell division uses the modified gene, even though it is foreign to the organism. Transgenic research has been completed on many different organisms and the focus of this text will be genetic modification of animals. There are many pros and cons to transgenic or genetic engineering in species of animals. Jaenish (1988) states to the American Association for the Advancement of Science that, “The information gained from the use of the transgenic technology is relevant to almost any aspect of modern biology including developmental gene regulation, the action of oncogenes, the immune system, and mammalian development” (p, 1468). There are also many cons with the production of transgenic organism. Cons involved in transgenic research can include: mutations on organisms, the creation of new species potentially may blur the species boundaries, the long term Running Head: TRANSGENICS 4 effects on the organism and the environment, and unintentional personal, social, and cultural consequences (Glenn, 2004, para.1). The organism that the research is tested on could bring many benefits to society, but the safety of the experiments or the gene mutations of genetic engineering techniques are not looked upon when the testing begins. The organism may be enduring intense pain or other changes that cannot be prevented because the safety features are not understood or agreed on by scientists and the public as a whole. They will also not have any valuable input on the effects that the transgenic research has nor can the research be completely reversed if a problem occurs because safety is not a main focus in the genetic engineering of an animal. This paper argues that present genetic engineering of species through transgenic research is ethically wrong due to the lack of information given to the general public, causing the De Minimis Dilemma, which states that individuals hold different views of safety. Without the proper safety precautions, animals could be harmed without the general public knowing the risks that the animals are undergoing. The pros and cons will be reviewed in this research paper and the value of safety will ethically dismantle the argument supporting the genetic engineering of an organism for the benefit of humans. One of the many pros of genetic engineering or transgenic research on animals is the fact that many human and other diseases found in organisms can be studied in more detail in search of a cure. Many studies are completed by scientists to discover cures for diseases like renal disease. Medicine is ever changing and the use of animals to research the genes and how a slight modification in the gene pool could prevent or aid in the symptoms of a disease. Scientists perform genetic engineering techniques on organisms to find the solutions to medical issues that humans face around the world, and find the most effective solutions for the creation of medicine and cures. Other medical aspects that transgenic organisms are included in are: transplant organs Running Head: TRANSGENICS 5 by aiding in the production of an exact match, nutritional supplements and pharmaceuticals through modified animal milk, and aiding in the production of red blood cells. A study completed in 2005 about the end stages of renal diseases stated, “Although the use of these animals (mainly knockouts) has highlighted some pitfalls of this approach (compensation by closely related gene products, absence of temporal knockouts) it has brought important information about the role of specific gene-products…” (Bascands & Schanstra, 2005, p. 925). Even though the study proved that the animals may have suffered some knock-outs and other pitfalls, researchers found many benefits on how to aid those who suffer from renal disease. Further use of these animals, especially in combination with pharmacologic tools, produces molecules and process that gave scientists the necessary knowledge needed to find a medicine for the diseases that humans and other organisms suffer from. The research helped scientists find many factors that cause the symptoms of renal disease and they can better find a solution with the signs that the animals produced (Bascands & Schanstra, 2005, p. 925). Patients die every day because of the lack of transplant organs available. Transgenic pigs may become the solution to the shortage of hearts, livers, and other transplant organs that are desperately needed. Endang Tri Margawati (2003) says, “Currently, xenotransplantation is hampered by a pig protein that can cause donor rejection but research is underway to remove the pig protein and replace it with a human protein” (para. 21). The pig’s genes will be engineered to suit the human, and the organs will be modified by removing aspects of the pig that would not be sustained in the body of a human or other organism. The organism will then be given the organ and since the pig aspects will be removed, it will be able to function as the organ needed by the transplant patient. Running Head: TRANSGENICS 6 Another aspect of medicine that benefits from the use of transgenic animals is that animal milk can be changed by the use of transgenics to aid in the creation of supplements and pharmaceuticals that can benefit humans and other organisms. Products such as insulin, growth hormone, and blood anti-clotting factors may soon be or have already been obtained by the milk of transgenic animals. It is “underway to manufacture milk through transgenesis for treatment of debilitating diseases such as phenylketonuria (PKU), hereditary emphysema, and cystic fibrosis” (Margawati, 2003, para. 22). These diseases can have solutions with the use of a product that animals naturally produce, just by altering their genes to sustain the supplements that are needed in suffering patients. The milk of the transgenic animal will have the nutrients that a patient needs and will create the modifications needed for a patient to live a better life through the consumption of the supplements in the genetically modified organism. Finally, the research of transgenics for the use of medicine is concluded by the reproduction of red blood cells in the human body. With the use of milk of a transgenic organism, scientists have reason to believe that they can discover a way to reproduce red blood cells. It will add a normal copy of a gene that produces non-working red blood cells with a copy of the same gene that is proper working order (Margawati, 2003, para. 24). This will aid in finding cures for over 5,000 named genetic diseases and many other issues that can affect an organism; also allowing scientists to find a solution to help patients suffering from red blood cell malfunctions. Agricultural applications are also greatly affected by the use of transgenic animals. Herds with desired traits can be manufactured by genetic engineering. Traditional selective breeding is difficult and risky, but with transgenic research, scientists have discovered ways to modify genes in organisms to show a desired trait without the time consuming task of selective Running Head: TRANSGENICS 7 breeding. Scientists can also use the genetic engineering techniques to make livestock larger and less resistant to disease. Just like the medical research completed by Bascands and Schanstra (2005), other animals can have genes added to their gene pool to produce lower chances of contracting a disease (p. 927). Scientists will target the genes within the animal and find another gene to replace with the mutated gene to solve any disease issues that an organism may face (Margawati, 2003, para.
Recommended publications
  • CRISPR and the Future of Fertility Innovation
    Science and Technology Law Review Volume 23 Number 1 Article 3 2020 CRISPR and the Future of Fertility Innovation June R. Carbone University of Minnesota Law School, [email protected] Follow this and additional works at: https://scholar.smu.edu/scitech Part of the Health Law and Policy Commons, and the Science and Technology Law Commons Recommended Citation June R Carbone, CRISPR and the Future of Fertility Innovation, 23 SMU SCI. & TECH. L. REV. 31 (2020) https://scholar.smu.edu/scitech/vol23/iss1/3 This Article is brought to you for free and open access by the Law Journals at SMU Scholar. It has been accepted for inclusion in Science and Technology Law Review by an authorized administrator of SMU Scholar. For more information, please visit http://digitalrepository.smu.edu. CRISPR and the Future of Fertility Innovation June Carbone* In 2018, Dr. He Jiankui announced that he had used CRISPR, a gene- editing tool, to produce newborn twin girls with the gene for HIV resistance.1 The announcement caused a global uproar. Dr. He appeared to have tried the procedure without advance testing.2 He did so without assurance the proce- dure was safe; indeed, unintended side effects could affect not only the twins but the twins’ own offspring.3 And he did it to otherwise healthy embryos.4 While the twins risked exposure to the HIV virus their father carried, less risky treatments exist that reduce the risk of transmission.5 Dr. He also tried the technique without following appropriate Chinese protocols.6 As a result of the outcry that followed his announcement, use of the procedure in China has been effectively shut down.7 This leaves open the question: if CRISPR is to be used again in the reproductive context, how and why is it to occur? CRISPR creates new possibilities for genetic engineering, which alters a person’s—or an embryo’s—genetic inheritance in ways that alter the germline, in turn passing on the alterations to subsequent generations.
    [Show full text]
  • CRISPR Technology; Advantages, Limitations and Future Direction
    nd Ph l a arm Omodamilola and Ibrahim, J Biomed Pharm Sci 2018, 1:2 a a ic c d e e u m t i o c Journal of i a B l S f o c l i e a n n c r e u s o J Biomedical and Pharmaceutical Sciences Review Article Open Access CRISPR Technology: Advantages, Limitations and Future Direction Omoyayi Ibrahim Omodamilola* and Abdullahi Umar Ibrahim Department of Biomedical Engineering, Near East University, Mersin 10, Turkey Abstract The evolutionary discovery of CRIPRS technology has paved the way for researchers in various fields’ genetics, medicine, pharmacy and computer science. Its potential application is limitless spanning from therapy of disease such as cancer and immunotherapy with gene silencing, gene knock down, gene KO, to the food production of genetically modified foods, the potential possibility of genetically designing baby using CRSIPR technology with enhanced trait and potential of eradicating Malaria and HIV-AIDS. The review thereby focuses on Off-targets limitation of the technology which is explained as one of the major constraint for application in clinical procedure with its hope of eradication through machine learning (ML). Further application of crisper technology was also discussed. Keywords: CRISPR; Designer Baby; Machine Learning; Off Targets; of an adaptive immune system and the discovery of Cas9 and PAM by Gene Knock out Bolotin. The process where bacterial CRISPR transcribed a guide RNA and form CRISPR-Cas9 Complex which not only store a record of Introduction invading bacteriophages and other viral DNA but also to destroy the The word “smart” has been the recent trend in almost all viruses upon second attack [6].
    [Show full text]
  • 1 Designer Babies
    Designer Babies: The Ethical and Societal Effects Andy Kromer College of Saint Benedict/Saint John’s University April 17, 2018 It’s a process; It dates back to 12,000 BC when human beings started domesticating animals. Unknowingly, at the time, we participated in an act of science: genetic modification. It is a process in which humans influence the genes of another specie. Many believe this process is the same as genetic engineering; however, there is a difference. Genetic engineering is defined as the artificial modification or manipulation of an organism’s nucleic acids or DNA. The difference is the matter in which the genes are manipulated. Through genetic modification, natural changes are made to a specie, while through genetic engineering, tools or technologies are used to modify or manipulate a certain gene. The process of genetic engineering isn’t natural. This is a key component that set these two terms apart, but they are very similar nonetheless. Background: Genetic Engineering Genetic engineering was first introduced nearly fifty years ago by Herbert Boyer and Stanley Cohen. At first, this technology was used on plants to increase the yield values of certain farm crops. Undoubtedly, it has provided a great advancement in the economy. Brookes and Barfoot (2014) found that since the first significant amounts of genetically modified crops were planted in 1996, there has been more than one hundred and sixty-six billion dollars generated from the agriculture industry. The production levels have also increased substantially. The success of GMOs and genetic engineering has sparked curiosity in the United States.
    [Show full text]
  • Are We Ready for Designer Babies? Analysis of Law, Policy and Ethics Surrounding Germline Genetic Engineering
    MUMBAI SILICON VALLEY BANGALORE SINGAPORE MUMBAI BKC NEW DELHI MUNICH NEW YORK Are we ready for Designer Babies? Analysis of law, policy and ethics surrounding germline genetic engineering Strategic, Legal, Tax and Ethical issues June 2019 © Copyright 2019 Nishith Desai Associates www.nishithdesai.com Are we ready for Designer Babies? Analysis of law, policy and ethics surrounding germline genetic engineering Strategic, Legal, Tax and Ethical Issues June 2019 [email protected] DMS Code: No 480049v2 © Nishith Desai Associates 2019 Are we ready for Designer Babies? Analysis of law, policy and ethics surrounding germline genetic engineering About NDA At Nishith Desai Associates, we have earned the reputation of being Asia’s most Innovative Law Firm – and the go-to specialists for companies around the world, looking to conduct businesses in India and for Indian companies considering business expansion abroad. In fact, we have conceptualized and created a state-of-the-art Blue Sky Thinking and Research Campus, Imaginarium Aligunjan, an international institution dedicated to designing a premeditated future with an embedded strategic foresight capability. We are a research and strategy driven international firm with offices in Mumbai, Palo Alto (Silicon Valley), Bangalore, Singapore, New Delhi, Munich, and New York. Our team comprises of specialists who provide strategic advice on legal, regulatory, and tax related matters in an integrated manner basis key insights carefully culled from the allied industries. As an active participant in shaping India’s regulatory environment, we at NDA, have the expertise and more importantly – the VISION – to navigate its complexities. Our ongoing endeavors in conducting and facilitating original research in emerging areas of law has helped us develop unparalleled proficiency to anticipate legal obstacles, mitigate potential risks and identify new opportunities for our clients on a global scale.
    [Show full text]
  • Pencil Template
    www.xplora.org Xplora Thematic dossier: DNA by Alexa Joyce – [email protected] Every month, Xplora will release a new thematic dossier on an important topic in science, complete with background information, recommended resources, experiments, training opportunities and more. This month the focus is DNA – it includes top tips for extracting DNA from bananas, animations for illustrating key aspects and more. Until just over 50 years ago, nobody knew what deoxyribonucleic acid (DNA) was. Now, DNA is one of the hottest topics in science and hits the headlines every day. Researchers James Watson, Francis Crick, Maurice Wilkins and Rosalind Franklin each contributed essential work to discover this special molecule, which is found in the nucleus of every living cell. DNA is the template for cells to produce the proteins and other molecules that make the cell machinery work smoothly. Without DNA, no cells would even exist, whether plants, animals or humans. Profiling the DNA of an organism helps us to understand how it works, by getting an insight into the kinds of proteins that the organism builds and uses. It can also help to understand disease, by comparing healthy genes with those that cause health problems. However DNA profiling techniques will challenge our society in new ways. For instance, if a DNA profile shows that a patient will die young because of a disease, should the patient be informed? And who else should receive DNA profile information – for instance the police, health insurance companies or others? DNA profiles could encourage discrimination – a company boss might reject a new applicant for a job if she has a gene for mental illness, even if the person has never suffered from the problem.
    [Show full text]
  • Is Germline Gene Editing Exceptional?
    William & Mary Law School William & Mary Law School Scholarship Repository Faculty Publications Faculty and Deans 2021 Is Germline Gene Editing Exceptional? Myrisha S. Lewis William & Mary Law School, [email protected] Follow this and additional works at: https://scholarship.law.wm.edu/facpubs Part of the Bioethics and Medical Ethics Commons, Food and Drug Law Commons, Health Law and Policy Commons, and the Science and Technology Law Commons Repository Citation Lewis, Myrisha S., "Is Germline Gene Editing Exceptional?" (2021). Faculty Publications. 2028. https://scholarship.law.wm.edu/facpubs/2028 Copyright c 2021 by the authors. This article is brought to you by the William & Mary Law School Scholarship Repository. https://scholarship.law.wm.edu/facpubs Is Germline Gene Editing Exceptional? Myrisha S. Lewis' Advances in gene editing have recently received significantscientific and media attention. Gene editing, especially CRISPR-Cas9, has revived multiple longstanding ethical debates, including debates related to parental autonomy, health disparities, disability perspectives, and racial and economic inequalities. Germline, or heritable,gene editinggenerates several newer, neglected bioethical debates, including those about the shared human germline and whether there is a "line" that humans should not cross. ThisArticle addressesseveral interrelatedethical and legal questions related to germline gene editing. Those questions address why, if at all, germline gene editing needs to be regulated and, ifgermline gene editing needs to be regulated, whether it can be regulated under existing law. Ultimately, this Article finds thatgermline gene editing should and can be regulated under existing law; however, the currentfederal-centric regime is not the optimal way to regulate this subset ofgene editing.
    [Show full text]
  • Science and Bioethics of CRISPR-Cas9 Gene Editing: an Analysis Towards Separating Facts and Fiction
    YALE JOURNAL OF BIOLOGY AND MEDICINE 90 (2017), pp.625-634. Review Science and Bioethics of CRISPR-Cas9 Gene Editing: An Analysis Towards Separating Facts and Fiction Adam P. Cribbsa,c,* and Sumeth M. W. Pererab,c aComputational Genomics and Training Centre (CGAT), MRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Headington, Oxford, UK;b Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK; cCampion Hall, Oxford, UK Since its emergence in 2012, the genome editing technique known as CRISPR-Cas9 and its scientific use have rapidly expanded globally within a very short period of time. The technique consists of using an RNA guide molecule to bind to complementary DNA sequences, which simultaneously recruits the endonuclease Cas9 to introduce double-stranded breaks in the target DNA. The resulting double- stranded break is then repaired, allowing modification or removal of specific DNA bases. The technique has gained momentum in the laboratory because it is cheap, quick, and easy to use. Moreover, it is also being applied in vivo to generate more complex animal model systems. Such use of genome editing has proven to be highly effective and warrants a potential therapy for both genetic and non-genetic diseases. Although genome editing has the potential to be a transformative therapy for patients it is still in its infancy. Consequently, the legal and ethical frameworks are yet to be fully discussed and will be an increasingly important topic as the technology moves towards more contentious issues such as modification of the germline. Here, we review a number of scientific and ethical issues which may potentially influence the development of both the technology and its use in the clinical setting.
    [Show full text]
  • Designer Babies
    DESIGNER BABIES. A QUESTION OF ETHICS Justo Aznar MD, Ph D. Institute of Life´s Science of the Catholic University of Valencia, Spain. INTRODUCTION One of the most interesting biomedical advances brought about by new technologies in recent years, and with undoubtedly the greatest social repercussion, is preimplantation genetic screening1. This technique has two fundamental applications: to produce babies free of a hereditary or genetic disease that their parents may have2,3 and the production of designer babies4. The term “designer babies” may be used to refer to a range of reproductive techniques including the use of sex selection techniques to prevent the birth of children with x-linked diseases, preimplantation genetic diagnosis to select for embryos free from genetic disorders, selection techniques for eggs, sperm or embryo donors with particular characteristics, and the enhancement of features such as intelligence, sporting ability or attractiveness. However, when discussing designer babies in this article, we will refer to a brother or sister produced by in-vitro fertilisation, capable of donating live-saving tissue to an existing child. The production and subsequent use of designer babies has provoked widespread social debate, since trying to find a means to cure those sick siblings is something which is not only accepted, but also desired by a large part of society. 1 However, the production of designer babies entails specific medical5 and ethical6 problems. In this article, we will essentially address the latter. At the start of this reflection, I believe it is necessary to point out that for the parents of a sick child, producing a designer baby i.e.
    [Show full text]
  • Politically Correct Eugenics
    FIU Law Review Volume 12 Number 1 Article 7 Fall 2016 Politically Correct Eugenics Seema Mohapatra Barry University Dwayne O. Andreas School of Law Follow this and additional works at: https://ecollections.law.fiu.edu/lawreview Part of the Other Law Commons Online ISSN: 2643-7759 Recommended Citation Seema Mohapatra, Politically Correct Eugenics, 12 FIU L. Rev. 51 (2016). DOI: https://dx.doi.org/10.25148/lawrev.12.1.7 This Article is brought to you for free and open access by eCollections. It has been accepted for inclusion in FIU Law Review by an authorized editor of eCollections. For more information, please contact [email protected]. 04-MOHAPATRA 5.9.17.DOCX (DO NOT DELETE) 5/17/17 2:44 PM POLITICALLY CORRECT EUGENICS Seema Mohapatra* INTRODUCTION Eugenics is a loaded word bringing to mind the horrors of Nazi Germany and here in the United States, our history of forced sterilizations. Although eugenics has a negative connotation, family balancing (the term of art coined to refer to those who use preimplantation genetic diagnosis to pick an embryo of a certain gender) does not. In fact, it sounds empowering to be able to have a say in the gender of one’s baby. This Article explores new innovations in life sciences that make eugenics inevitable—for a certain class of people—those who can afford to pay for it. The designer baby thought experiment has been around for several decades, but until very recently the idea of actually being able to enhance an embryo was still very much science fiction.
    [Show full text]
  • Designer Babies: the Eedn for Regulation on the Quest for Perfection Jenifer V
    Seton Hall University eRepository @ Seton Hall Law School Student Scholarship Seton Hall Law 5-1-2014 Designer Babies: The eedN for Regulation on the Quest For Perfection Jenifer V. Turriziani Follow this and additional works at: https://scholarship.shu.edu/student_scholarship Recommended Citation Turriziani, Jenifer V., "Designer Babies: The eN ed for Regulation on the Quest For Perfection" (2014). Law School Student Scholarship. 595. https://scholarship.shu.edu/student_scholarship/595 Jenifer Turriziani Designer Babies: The Need for Regulation on the Quest For Perfection Imagine a society where the ability to create the “perfect child” is a possibility. With recent advances in reproductive medicine, parents may one day be able to customize their child’s embryos. In 2004 the term “designer baby” was added to the Oxford English Dictionary, where it is defined as “a baby whose genetic makeup has been selected in order to eradicate a particular defect, or to ensure that a particular gene is present.”1 At this time, the creation of designer babies is not yet possible. However, in the future by using Preimplantation Genetic Diagnosis (PGD) in conjunction with In Vitro Fertilization (IVF) doctors may have the ability to create “designer babies.” Assisted Reproductive Technologies (ART), such as IVF and PGD, are most often enlisted by infertile couples. PGD can determine which embryos are affected by which genetic conditions before implantation. This process ensures that only embryos that test clear of inheritable diseases are transferred to the uterus using IVF. While those that carry the harmful genes will be discarded prior to implantation. Currently, PGD and IVF have been used to prevent couples from giving birth to a child afflicted with genetic disease.
    [Show full text]
  • Is Germline Gene Editing Exceptional?
    LEWIS_FORMATTED (DO NOT DELETE) 12/29/2020 8:27 PM Is Germline Gene Editing Exceptional? Myrisha S. Lewis* Advances in gene editing have recently received significant scientific and media attention. Gene editing, especially CRISPR-Cas9, has revived multiple longstanding ethical debates, including debates related to parental autonomy, health disparities, disability perspectives, and racial and economic inequalities. Germline, or heritable, gene editing generates several newer, neglected bioethical debates, including those about the shared human germline and whether there is a “line” that humans should not cross. This Article addresses several interrelated ethical and legal questions related to germline gene editing. Those questions address why, if at all, germline gene editing needs to be regulated and, if germline gene editing needs to be regulated, whether it can be regulated under existing law. Ultimately, this Article finds that germline gene editing should and can be regulated under existing law; however, the current federal-centric regime is not the optimal way to regulate this subset of gene editing. Instead, this Article argues that germline gene editing should be regulated like traditional assisted reproductive technology, such as in vitro fertilization, instead of as an exceptional, federally-regulated medical product. Doing so would reduce regulatory barriers in access to innovation, and the technique would be subject to a significantly less burdensome and less federally dominated regime than it is today. Additionally, this Article’s proposed regulatory treatment of germline gene editing would increase access to the technique and remove the *Associate Professor, William & Mary Law School; J.D., Columbia Law School; A.B., Harvard College. For their helpful comments and suggestions, I thank Aaron Bruhl, I.
    [Show full text]
  • Transgenic Animals
    IQP – 43 - DSA - 3001 IQP – 43 - DSA - 1845 IQP – 43 - DSA - 6882 IQP – 43 - DSA - 0994 TRANSGENIC ANIMALS An Interactive Qualifying Project Report Submitted to the Faculty of WORCESTER POLYTECHNIC INSTITUTE In partial fulfillment of the requirement for the Degree of Bachelor of Science By: _______________ _______________ _______________ _______________ Marcella Corcoran Nicholas Maloney Whitney Moore Sara Munro August 25, 2004 APPROVED: ______________________ Prof. David S. Adams, Ph.D. Project Advisor 1 ABSTRACT Transgenic animals are animals that have been genetically altered by inserting a transgene into their genomes to express a new trait. This IQP provides an overview of the construction of transgenic animals, the categories they fall into, and notable examples of each type. The effects of this new technology on both science and society were investigated by describing current ethical and legal debates. Finally, conclusions were formulated based on our research. 2 TABLE OF CONTENTS Page Signature Page…………………………………………………………………………………..1 Abstract………………………………………………………………………………………… 2 Table of Contents………………………………………………………………………………..3 Executive Summary……………………………………………………………………………..4 Project Objective………………………………………………………………………………...7 Chapter 1: Transgenic Animal Description and Construction…………………………………..8 Chapter 2: Transgenic Animal Classification and Examples…………………………………..18 Chapter 3: Transgenic Ethics…………………………………………………………………...37 Chapter 4: Transgenic Legalities……………………………………………………………….57 Chapter 5: Conclusions…………………………………………………………………………67
    [Show full text]