Literature DB >> 28777929

Human Germline Genome Editing.

Kelly E Ormond1, Douglas P Mortlock2, Derek T Scholes3, Yvonne Bombard4, Lawrence C Brody5, W Andrew Faucett6, Nanibaa' A Garrison7, Laura Hercher8, Rosario Isasi9, Anna Middleton10, Kiran Musunuru11, Daniel Shriner12, Alice Virani13, Caroline E Young3.   

Abstract

With CRISPR/Cas9 and other genome-editing technologies, successful somatic and germline genome editing are becoming feasible. To respond, an American Society of Human Genetics (ASHG) workgroup developed this position statement, which was approved by the ASHG Board in March 2017. The workgroup included representatives from the UK Association of Genetic Nurses and Counsellors, Canadian Association of Genetic Counsellors, International Genetic Epidemiology Society, and US National Society of Genetic Counselors. These groups, as well as the American Society for Reproductive Medicine, Asia Pacific Society of Human Genetics, British Society for Genetic Medicine, Human Genetics Society of Australasia, Professional Society of Genetic Counselors in Asia, and Southern African Society for Human Genetics, endorsed the final statement. The statement includes the following positions. (1) At this time, given the nature and number of unanswered scientific, ethical, and policy questions, it is inappropriate to perform germline gene editing that culminates in human pregnancy. (2) Currently, there is no reason to prohibit in vitro germline genome editing on human embryos and gametes, with appropriate oversight and consent from donors, to facilitate research on the possible future clinical applications of gene editing. There should be no prohibition on making public funds available to support this research. (3) Future clinical application of human germline genome editing should not proceed unless, at a minimum, there is (a) a compelling medical rationale, (b) an evidence base that supports its clinical use, (c) an ethical justification, and (d) a transparent public process to solicit and incorporate stakeholder input.
Copyright © 2017 American Society of Human Genetics. All rights reserved.

Entities:  

Keywords:  CRISPR; ethics; eugenics; gene editing; gene therapy; genetics policy; genome editing; germline; human genome; society

Mesh:

Year:  2017        PMID: 28777929      PMCID: PMC5544380          DOI: 10.1016/j.ajhg.2017.06.012

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  49 in total

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3.  Generation of gene-modified cynomolgus monkey via Cas9/RNA-mediated gene targeting in one-cell embryos.

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5.  Permanent alteration of PCSK9 with in vivo CRISPR-Cas9 genome editing.

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6.  Enhanced efficiency of human pluripotent stem cell genome editing through replacing TALENs with CRISPRs.

Authors:  Qiurong Ding; Stephanie N Regan; Yulei Xia; Leoníe A Oostrom; Chad A Cowan; Kiran Musunuru
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7.  The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Initiative: methods of the EGAPP Working Group.

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8.  CAS9 transcriptional activators for target specificity screening and paired nickases for cooperative genome engineering.

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Review 9.  International regulatory landscape and integration of corrective genome editing into in vitro fertilization.

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Journal:  Reprod Biol Endocrinol       Date:  2014-11-24       Impact factor: 5.211

10.  RNA-programmed genome editing in human cells.

Authors:  Martin Jinek; Alexandra East; Aaron Cheng; Steven Lin; Enbo Ma; Jennifer Doudna
Journal:  Elife       Date:  2013-01-29       Impact factor: 8.140

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3.  Risks and benefits of human germline genome editing: An ethical analysis.

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Review 4.  Gene Editing and Gene-Based Therapeutics for Cardiomyopathies.

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5.  Better beings?

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6.  Gene therapy: Human genome editing in heart disease.

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7.  Genetics: Human genome editing in heart disease.

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Review 8.  CRISPR/Cas9 facilitates genomic editing for large-scale functional studies in pluripotent stem cell cultures.

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Review 9.  Intergenerational transmission of the effects of maternal exposure to childhood maltreatment on offspring obesity risk: A fetal programming perspective.

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10.  Revising, Correcting, and Transferring Genes.

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