Cloning Human Beings
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Welfare Issues with Genetic Engineering and Cloning of Farm Animals
WellBeing International WBI Studies Repository 2006 Welfare Issues with Genetic Engineering and Cloning of Farm Animals The Humane Society of the United States Follow this and additional works at: https://www.wellbeingintlstudiesrepository.org/ hsus_reps_impacts_on_animals Part of the Animal Studies Commons, Bioethics and Medical Ethics Commons, and the Other Genetics and Genomics Commons Recommended Citation The Humane Society of the United States, "Welfare Issues with Genetic Engineering and Cloning of Farm Animals" (2006). IMPACTS ON FARM ANIMALS. 21. https://www.wellbeingintlstudiesrepository.org/hsus_reps_impacts_on_animals/21 This material is brought to you for free and open access by WellBeing International. It has been accepted for inclusion by an authorized administrator of the WBI Studies Repository. For more information, please contact [email protected]. Farm Animal Welfare • The HSUS 2100 L St., N.W. • Washington, DC 20037 • HSUS.org 202-452-1100 • F: 301-258-3081 • FarmAnimalWelfare.org An HSUS Report: Welfare Issues with Genetic Engineering and Cloning of Farm Animals Abstract Developments in biotechnology have raised new concerns about animal welfare, as farm animals now have their genomes modified (genetically engineered) or copied (cloned) to propagate certain traits useful to agribusiness, such as meat yield or feed conversion. These animals suffer from unusually high rates of birth defects, disabili- ties, and premature death. Genetically engineering farm animals for greater bone strength or reduced pain reception, for example, may result in improved well-being, yet the broad use of this technology often causes increased suffering. The limited success of gene insertion techniques can result in genes failing to reach target cells and finishing in cells of unintended organs, and abnormally developed embryos may die in utero, be infertile, or born with development defects, attributable in part to insertional problems. -
Stem Cells Cloning Prons & Cons
& Trans g ge in n n e s o l i s C Cloning and Transgenesis Kalodimou, Clon Transgen 2014, 3:3 ISSN: 2168-9849 DOI: 10.4172/2168-9849.1000127 Short Communication Open Access Stem Cells Cloning Prons & Cons Vasiliki E Kalodimou* Research and Regenerative Medicine Department, IASO Maternity Hospital, Athens, Greece *Corresponding author: Vasiliki E Kalodimou, Head of Flow Cytometry-Research and Regenerative Medicine Department, IASO Maternity Hospital, Athens, Greece, Tel: 0030-210-618-5; E-mail: [email protected] Rec date: May 16, 2014; Acc date: Jun 30, 2014; Pub date: July 2, 2014 Copyright: © 2014 Kalodimou VE. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Stem Cell Cloning the target cell. In principle, this may be dangerous, because the gene therapy vector can potentially modify the activity of neighboring genes Over the last several decades, the ideas of both stem cell research (positively or negatively) in close proximity to the insertion site or and cloning have received significantly more attention than ever even inactivate host genes by integrating into them [6]. These before; currently there are 23 open/completed clinical trials, together phenomena may contribute to the malignant transformation of the with a great deal of controversy. This new advances in medical targeted cells, ultimately resulting in cancer. Another major limitation technology had provide scientific with a new view of potential to help of using adult stem cells is that it is relatively difficult to maintain the people suffering from various diseases as well as to help them recover stem cell state during ex vivo manipulations. -
Human Cloning: Must We Sacrifice Medical Research in the Name of a Total Ban?
S. HRG. 107–812 HUMAN CLONING: MUST WE SACRIFICE MEDICAL RESEARCH IN THE NAME OF A TOTAL BAN? HEARING BEFORE THE COMMITTEE ON THE JUDICIARY UNITED STATES SENATE ONE HUNDRED SEVENTH CONGRESS SECOND SESSION FEBRUARY 5, 2002 Serial No. J–107–55 Printed for the use of the Committee on the Judiciary ( U.S. GOVERNMENT PRINTING OFFICE 83–684 PDF WASHINGTON : 2002 For sale by the Superintendent of Documents, U.S. Government Printing Office Internet: bookstore.gpo.gov Phone: toll free (866) 512–1800; DC area (202) 512–1800 Fax: (202) 512–2250 Mail: Stop SSOP, Washington, DC 20402–0001 VerDate Feb 1 2002 09:13 Jan 16, 2003 Jkt 083684 PO 00000 Frm 00001 Fmt 5011 Sfmt 5011 C:\HEARINGS\83684.TXT SJUD4 PsN: CMORC COMMITTEE ON THE JUDICIARY PATRICK J. LEAHY, Vermont, Chairman EDWARD M. KENNEDY, Massachusetts ORRIN G. HATCH, Utah JOSEPH R. BIDEN, JR., Delaware STROM THURMOND, South Carolina HERBERT KOHL, Wisconsin CHARLES E. GRASSLEY, Iowa DIANNE FEINSTEIN, California ARLEN SPECTER, Pennsylvania RUSSELL D. FEINGOLD, Wisconsin JON KYL, Arizona CHARLES E. SCHUMER, New York MIKE DEWINE, Ohio RICHARD J. DURBIN, Illinois JEFF SESSIONS, Alabama MARIA CANTWELL, Washington SAM BROWNBACK, Kansas JOHN EDWARDS, North Carolina MITCH MCCONNELL, Kentucky BRUCE A. COHEN, Majority Chief Counsel and Staff Director SHARON PROST, Minority Chief Counsel MAKAN DELRAHIM, Minority Staff Director (II) VerDate Feb 1 2002 09:13 Jan 16, 2003 Jkt 083684 PO 00000 Frm 00002 Fmt 5904 Sfmt 5904 C:\HEARINGS\83684.TXT SJUD4 PsN: CMORC C O N T E N T S STATEMENTS OF COMMITTEE MEMBERS Page Brownback, Hon. -
Cloning: Adult Vs. Embryonic Cells and Techniques Employed
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Supervised Undergraduate Student Research Chancellor’s Honors Program Projects and Creative Work Spring 5-2001 Cloning: Adult vs. Embryonic Cells and Techniques Employed Rebecca Ruth Frazor University of Tennessee-Knoxville Follow this and additional works at: https://trace.tennessee.edu/utk_chanhonoproj Recommended Citation Frazor, Rebecca Ruth, "Cloning: Adult vs. Embryonic Cells and Techniques Employed" (2001). Chancellor’s Honors Program Projects. https://trace.tennessee.edu/utk_chanhonoproj/459 This is brought to you for free and open access by the Supervised Undergraduate Student Research and Creative Work at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Chancellor’s Honors Program Projects by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. UNIVERSITY HONORS PROGRAM SENIOR PROJECT - APPROVAL Name: Getec eCA f?- f(CAZOr College: AQn eMi:hA rv Department: A1 (met I SCi!A1w -J Faculty Mentor: F. N-S ChV\C ¥: PROJECT TITLE: C10l/1\(}q : Adult \[) ' fmmrVVl l0 C l, (( ~ ~rd the. ~ Qr\L\A<; Icchn \ quc ~ Emplo\( f d I have reviewed this completed senior honors thesis with this student and certify that it is a project commens rate with rs level undergraduate research in this field. Signed: ;. ./-1 Faculty Mentor Date: _-+-'""-+----L-___ Comments (Optional): Cloning: Adult vs. Embryonic Cells and Various Techniques Employed Rebecca R. Frazor Mentor: F. Neal Schrick Senior Honors Project May 2001 Abstract The cloning of amphibians and mainly mammals is discussed focusing on somatic cell usage. Significant progress has been made in recent years and this is outlined with an emphasis on techniques and their differences. -
Observation and a Numerical Study of Gravity Waves During Tropical Cyclone Ivan (2008)
Open Access Atmos. Chem. Phys., 14, 641–658, 2014 Atmospheric www.atmos-chem-phys.net/14/641/2014/ doi:10.5194/acp-14-641-2014 Chemistry © Author(s) 2014. CC Attribution 3.0 License. and Physics Observation and a numerical study of gravity waves during tropical cyclone Ivan (2008) F. Chane Ming1, C. Ibrahim1, C. Barthe1, S. Jolivet2, P. Keckhut3, Y.-A. Liou4, and Y. Kuleshov5,6 1Université de la Réunion, Laboratoire de l’Atmosphère et des Cyclones, UMR8105, CNRS-Météo France-Université, La Réunion, France 2Singapore Delft Water Alliance, National University of Singapore, Singapore, Singapore 3Laboratoire Atmosphères, Milieux, Observations Spatiales, UMR8190, Institut Pierre-Simon Laplace, Université Versailles-Saint Quentin, Guyancourt, France 4Center for Space and Remote Sensing Research, National Central University, Chung-Li 3200, Taiwan 5National Climate Centre, Bureau of Meteorology, Melbourne, Australia 6School of Mathematical and Geospatial Sciences, Royal Melbourne Institute of Technology (RMIT) University, Melbourne, Australia Correspondence to: F. Chane Ming ([email protected]) Received: 3 December 2012 – Published in Atmos. Chem. Phys. Discuss.: 24 April 2013 Revised: 21 November 2013 – Accepted: 2 December 2013 – Published: 22 January 2014 Abstract. Gravity waves (GWs) with horizontal wavelengths ber 1 vortex Rossby wave is suggested as a source of domi- of 32–2000 km are investigated during tropical cyclone (TC) nant inertia GW with horizontal wavelengths of 400–800 km, Ivan (2008) in the southwest Indian Ocean in the upper tropo- while shorter scale modes (100–200 km) located at northeast sphere (UT) and the lower stratosphere (LS) using observa- and southeast of the TC could be attributed to strong local- tional data sets, radiosonde and GPS radio occultation data, ized convection in spiral bands resulting from wave number 2 ECMWF analyses and simulations of the French numerical vortex Rossby waves. -
Hindu Bioethics for the Twenty-First Century
Journal of Hindu-Christian Studies Volume 14 Article 9 January 2001 Hindu Bioethics for the Twenty-First Century S. Cromwell Crawford Follow this and additional works at: https://digitalcommons.butler.edu/jhcs Part of the Religion Commons Recommended Citation Crawford, S. Cromwell (2001) "Hindu Bioethics for the Twenty-First Century," Journal of Hindu-Christian Studies: Vol. 14, Article 9. Available at: https://doi.org/10.7825/2164-6279.1252 The Journal of Hindu-Christian Studies is a publication of the Society for Hindu-Christian Studies. The digital version is made available by Digital Commons @ Butler University. For questions about the Journal or the Society, please contact [email protected]. For more information about Digital Commons @ Butler University, please contact [email protected]. -- Crawford: Hindu Bioethics for the Twenty-First Century Hindu Bioethics for the Twenty-First Century s. Cromwell Crawford University of Hawaii Introduction focus on these three distinctive features of Hindu bioethics, namely: its medical basis; IN his Cross Cultural Perspectives in its philosophical framework; its ethical Medical Ethics: Readings, Robert Veatch orientation. observes, "The religions of Judaism and Christianity and the secular thought of the Distinctive Features of Hindu Bioethics political philosophy of liberalism in the Anglo-American West are not the only Medical Basis alternatives to a Hippocratic medical ethic."J A unique feature of Hinduism is that a fully In fact, the new pluralistic approach to world fledged system of medicine evolved within .cultures is introducing us to several religious its complex ethos. The historical and philosophical alternatives from outside developments are shrouded in mystery due the Anglo-American West. -
Direct Cloning and Refactoring of a Silent Lipopeptide Biosynthetic Gene Cluster Yields the Antibiotic Taromycin A
Direct cloning and refactoring of a silent lipopeptide biosynthetic gene cluster yields the antibiotic taromycin A Kazuya Yamanakaa,b, Kirk A. Reynoldsa,c, Roland D. Kerstena, Katherine S. Ryana,d, David J. Gonzaleze, Victor Nizete,f, Pieter C. Dorresteina,c,f, and Bradley S. Moorea,f,1 aScripps Institution of Oceanography, University of California, San Diego, La Jolla, CA 92093; bYokohama Research Center, JNC Corporation, Yokohama 236-8605, Japan; cDepartment of Chemistry and Biochemistry, University of California, San Diego, La Jolla, CA 92093; dDepartment of Chemistry, University of British Columbia, Vancouver, BC, Canada V62 1Z4; and Departments of ePediatrics and fSkaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla, CA 92093 Edited by Jerrold Meinwald, Cornell University, Ithaca, NY, and approved December 23, 2013 (received for review October 23, 2013) Recent developments in next-generation sequencing technologies genes (9, 10). Synthetic biology approaches also can be used to have brought recognition of microbial genomes as a rich resource refactor orphan gene clusters by optimizing promoters, tran- for novel natural product discovery. However, owing to the scar- scriptional regulation, ribosome-binding sites, and even codon city of efficient procedures to connect genes to molecules, only use (11). Examples of successful regulatory gene manipulation to a small fraction of secondary metabolomes have been investigated elicit the production of new natural products from silent bio- to date. Transformation-associated recombination (TAR) cloning synthetic gene clusters in WT strains have been reported in takes advantage of the natural in vivo homologous recombination bacteria and fungi (12, 13); however, this approach requires the of Saccharomyces cerevisiae to directly capture large genomic loci. -
Dolly the Sheep – the First Cloned Adult Animal
DOLLY THE SHEEP – THE FIRST CLONED ADULT ANIMAL NEW TECHNOLOGY FOR IMPROVING LIVESTOCK From Squidonius via Wikimedia Commons In 1996, University of Edinburgh scientists celebrated the birth of Dolly the Sheep, the first mammal to be cloned using SCNT cloning is the only technology adult somatic cells. The Edinburgh team’s success followed available that enables generation of 99.8% its improvements to the single cell nuclear transfer (SCNT) genetically identical offspring from selected technique used in the cloning process. individuals of adult animals (including sterilized animals). As such, it is being Dolly became a scientific icon recognised worldwide and exploited as an efficient multiplication tool SCNT technology has spread around the world and has been to support specific breeding strategies of used to clone multiple farm animals. farm animals with exceptionally high genetic The cloning of livestock enables growing large quantities of value. the most productive, disease resistant animals, thus providing more food and other animal products. Sir Ian Wilmut (Inaugural Director of MRC Centre for Regeneration and Professor at CMVM, UoE) and colleagues worked on methods to create genetically improved livestock by manipulation of stem cells using nuclear transfer. Their research optimised interactions between the donor nucleus and the recipient cytoplasm at the time of fusion and during the first cell cycle. Nuclear donor cells were held in mitosis before being released and used as they were expected to be passing through G1 phase. CLONING IN COMMERCE, CONSERVATION OF AGRICULTURE AND PRESERVATION ANIMAL BREEDS OF LIVESTOCK DIVERSITY Cloning has been used to conserve several animal breeds in the recent past. -
Human Cloning, Genetic Engineering and Privacy
Curriculum Units by Fellows of the Yale-New Haven Teachers Institute 2000 Volume III: Constitutional and Statutory Privacy Protections in the 21st Century Human Cloning, Genetic Engineering and Privacy Curriculum Unit 00.03.07 by Carolyn Williams When news of a genetically engineered mouse with Down Syndrome (who died some time later) and the cloned sheep, Dolly hit the media, many wondered how these things were possible. Many undoubtedly thought them hoaxes or scientific experiments gone wrong. How many of us, outside of the scientific community had a clue that the next quest would involve the idea of cloning a human being or genetically engineering a better human, once the technology became available? Much of the technology is now available and with it comes a host of moral and ethical concerns. Is man playing God? Will clones become a subculture? Are we risking genetic disasters? Will this technology benefit all of society or just a select few? Cloned humans and genetically engineered bodies are the stuff that yesterday’s science fiction was made of. Today, they are current event topics and promise to become our medical future. We may not be morally prepared for these events, but the technology is here. Do we ignore it, try to regulate it, hope and pray that it goes away or do we embrace this new technology? RATIONALE This is a preliminary look into the biology, technology, ethics and conscious thought involved in human cloning and genetic engineering coupled with a brief exploration of governmental policy designed to regulate its research and practice. This study reports some of the current data for and against this new bio- technology and argues an individual’s constitutional right to privacy in choosing this technology. -
Artificial Development of Neural-Symbolic Networks
University of Exeter Department of Computer Science Artificial Development of Neural-Symbolic Networks Joseph Paul Townsend March 2014 Supervised by Dr. Ed Keedwell and Dr. Antony Galton Submitted by Joseph Paul Townsend, to the University of Exeter as a thesis for the degree of Doctor of Philosophy in Computer Science , March 2014. This thesis is available for Library use on the understanding that it is copyright material and that no quotation from the thesis may be published without proper acknowledgement. I certify that all material in this thesis which is not my own work has been identi- fied and that no material has previously been submitted and approved for the award of a degree by this or any other University. (signature) ................................................................................................. 1 Abstract Artificial neural networks (ANNs) and logic programs have both been suggested as means of modelling human cognition. While ANNs are adaptable and relatively noise resis- tant, the information they represent is distributed across various neurons and is therefore difficult to interpret. On the contrary, symbolic systems such as logic programs are in- terpretable but less adaptable. Human cognition is performed in a network of biological neurons and yet is capable of representing symbols, and therefore an ideal model would combine the strengths of the two approaches. This is the goal of Neural-Symbolic In- tegration [4, 16, 21, 40], in which ANNs are used to produce interpretable, adaptable representations of logic programs and other symbolic models. One neural-symbolic model of reasoning is SHRUTI [89, 95], argued to exhibit biological plausibility in that it captures some aspects of real biological processes. -
Multipotent Cell Types in Primary Fibroblast Cell Lines Used to Clone Pigs Using Somatic Cell Nuclear Transfer Sharon J
& Trans Harrison et al., Clon Transgen 2015, 4:2 g ge in n n e DOI: 10.4172/2168-9849.1000136 s o l i s C Cloning & Transgenesis ISSN: 2168-9849 Research Article Open Access Multipotent Cell Types in Primary Fibroblast Cell Lines Used to Clone Pigs using Somatic Cell Nuclear Transfer Sharon J. Harrison, Luke F.S. Beebe, Ivan Vassiliev, Stephen M. McIlfatrick and Mark B. Nottle* Reproductive Biotechnology Group, Centre for Stem Cell Research, Robinson Institute School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, South Australia, 5005, Australia Abstract We have previously demonstrated that the use of porcine mesenchymal stem cells (MSCs) isolated from the bone marrow can increase the proportion of somatic cell nuclear transfer (SCNT) embryos that develop to the blastocyst stage compared with adult fibroblasts obtained from the same animal. The aim of the present study was to determine if MSCs are also present in primary cultures of adult fibroblasts which are commonly used for cloning live animals. To do this we chose a primary culture of adult fibroblasts that we had previously used to clone pigs. Single cell clones were isolated using low-density plating. After seven days of culture 63% of colonies displayed typical fibroblast morphology, while the remainder appeared cobblestone-like in appearance. Two of the 57 clones that displayed fibroblast morphology differentiated into adipocytes but not chondrocytes or osteocytes (uni-potent clones). Three of the 33 cobblestone-like clones differentiated into chondrocytes only, while 3 differentiated into adipocytes and chondrocytes but not osteocytes (bi-potent clones). One of the bi-potent cobblestone-like clones was then used for SCNT and in vitro development compared with a fibroblast-like clone which did not differentiate. -
A Novel Generative Encoding for Evolving Modular, Regular and Scalable Networks
A Novel Generative Encoding for Evolving Modular, Regular and Scalable Networks Marcin Suchorzewski Jeff Clune Artificial Intelligence Laboratory Creative Machines Laboratory West Pomeranian University of Technology Cornell University [email protected] [email protected] ABSTRACT 1. INTRODUCTION In this paper we introduce the Developmental Symbolic En- Networks designed by humans and evolution have certain coding (DSE), a new generative encoding for evolving net- properties that are thought to enhance both their perfor- works (e.g. neural or boolean). DSE combines elements of mance and adaptability, such as modularity, regularity, hier- two powerful generative encodings, Cellular Encoding and archy, scalability, and being scale-free [12, 11, 1]. In this pa- HyperNEAT, in order to evolve networks that are modular, per we introduce a new generative representation called the regular, scale-free, and scalable. Generating networks with Developmental Symbolic Encoding that evolves networks these properties is important because they can enhance per- that possess these properties. We first review the mean- formance and evolvability. We test DSE’s ability to gener- ing of these terms before discussing them with respect to ate scale-free and modular networks by explicitly rewarding previous evolutionary algorithms. these properties and seeing whether evolution can produce Modularity is the encapsulation of function within mostly networks that possess them. We compare the networks DSE independently operating units, where the internal workings evolves to those of HyperNEAT. The results show that both of the module tend to only affect the rest of the structure encodings can produce scale-free networks, although DSE through the module’s inputs and outputs [12, 11].