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游击优生学:可遗传人类基因组编辑中的基因驱动

Guerrilla eugenics: gene drives in heritable human genome editing.

作者信息

Cutter Asher D

机构信息

Department of Ecology & Evolutionary Biology, University of Toronto, Toronto, Ontario, Canada

出版信息

J Med Ethics. 2023 Jul 4. doi: 10.1136/jme-2023-109061.

Abstract

CRISPR-Cas9 genome editing can and has altered human genomes, bringing bioethical debates about this capability to the forefront of philosophical and policy considerations. Here, I consider the underexplored implications of CRISPR-Cas9 gene drives for heritable human genome editing. Modification gene drives applied to heritable human genome editing would introduce a novel form of involuntary eugenic practice that I term guerrilla eugenics. Once introduced into a genome, stealth genetic editing by a gene drive genetic element would occur each subsequent generation irrespective of whether reproductive partners consent to it and irrespective of whether the genetic change confers any benefit. By overriding the ability to 'opt in' to genome editing, gene drives compromise the autonomy of carrier individuals and their reproductive partners to choose to use or avoid genome editing and impose additional burdens on those who hope to 'opt out' of further genome editing. High incidence of an initially rare gene drive in small human communities could occur within 200 years, with evolutionary fixation globally in a timeframe that is thousands of times sooner than achievable by non-drive germline editing. Following any introduction of heritable gene drives into human genomes, practices intended for surveillance or reversal also create fundamental ethical problems. Current policy guidelines do not comment explicitly on gene drives in humans. These considerations motivate an explicit moratorium as being warranted on gene drive development in heritable human genome editing.

摘要

CRISPR-Cas9基因组编辑能够且已经改变了人类基因组,使关于这种能力的生物伦理辩论成为哲学和政策考量的前沿问题。在此,我探讨了CRISPR-Cas9基因驱动对可遗传人类基因组编辑尚未充分探讨的影响。应用于可遗传人类基因组编辑的修饰基因驱动将引入一种新的非自愿优生实践形式,我将其称为“游击优生学”。一旦基因驱动元件被引入基因组,后续每一代都会发生由基因驱动元件进行的隐性基因编辑,无论生殖伴侣是否同意,也无论基因变化是否带来任何益处。通过凌驾于“选择参与”基因组编辑的能力之上,基因驱动损害了携带者个体及其生殖伴侣选择使用或避免基因组编辑的自主权,并给那些希望“选择退出”进一步基因组编辑的人带来额外负担。在小型人类群体中,一种最初罕见的基因驱动可能在200年内出现高发生率,在全球范围内实现进化固定的时间框架比非驱动种系编辑快数千倍。在将任何可遗传基因驱动引入人类基因组之后,旨在监测或逆转的做法也会引发基本的伦理问题。当前的政策指南并未明确评论人类基因驱动。这些考量促使有必要对可遗传人类基因组编辑中的基因驱动发展实行明确的暂停。

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