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2
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Nature. 2021 Aug;596(7873):583-589. doi: 10.1038/s41586-021-03819-2. Epub 2021 Jul 15.
3
Transcriptional adaptation in .在... 中进行转录适应。
Elife. 2020 Jan 17;9:e50014. doi: 10.7554/eLife.50014.
4
AlphaFold at CASP13.AlphaFold 在 CASP13 中的应用。
Bioinformatics. 2019 Nov 1;35(22):4862-4865. doi: 10.1093/bioinformatics/btz422.
5
Genetic compensation triggered by mutant mRNA degradation.突变 mRNA 降解引发的遗传补偿。
Nature. 2019 Apr;568(7751):193-197. doi: 10.1038/s41586-019-1064-z. Epub 2019 Apr 3.
6
PTC-bearing mRNA elicits a genetic compensation response via Upf3a and COMPASS components.PTC 携带的 mRNA 通过 Upf3a 和 COMPASS 成分引发遗传补偿反应。
Nature. 2019 Apr;568(7751):259-263. doi: 10.1038/s41586-019-1057-y. Epub 2019 Apr 3.
7
ahr2, But Not ahr1a or ahr1b, Is Required for Craniofacial and Fin Development and TCDD-dependent Cardiotoxicity in Zebrafish.ahr2,但不是 ahr1a 或 ahr1b,是斑马鱼颅面和鳍发育以及 TCDD 依赖性心脏毒性所必需的。
Toxicol Sci. 2019 Jul 1;170(1):25-44. doi: 10.1093/toxsci/kfz075.
8
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PLoS Genet. 2018 Feb 8;14(2):e1007212. doi: 10.1371/journal.pgen.1007212. eCollection 2018 Feb.
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Short body length phenotype is compensated by the upregulation of nidogen family members in a deleterious nid1a mutation of zebrafish.在斑马鱼的有害nid1a突变中,短体长表型通过巢蛋白家族成员的上调得到补偿。
J Genet Genomics. 2017 Nov 20;44(11):553-556. doi: 10.1016/j.jgg.2017.09.011. Epub 2017 Nov 11.
10
mRNA processing in mutant zebrafish lines generated by chemical and CRISPR-mediated mutagenesis produces unexpected transcripts that escape nonsense-mediated decay.通过化学诱变和CRISPR介导的诱变产生的突变斑马鱼品系中的mRNA加工产生了逃避无义介导衰变的意外转录本。
PLoS Genet. 2017 Nov 21;13(11):e1007105. doi: 10.1371/journal.pgen.1007105. eCollection 2017 Nov.

基于基因补偿的机制毒理学

Mechanistic toxicology in light of genetic compensation.

作者信息

Elizalde Mary Jane, Gorelick Daniel A

机构信息

Center for Precision Environmental Health, Department of Molecular & Cellular Biology, Baylor College of Medicine, Houston, Texas, USA.

出版信息

Toxicol Sci. 2023 Nov 6;197(2):115-20. doi: 10.1093/toxsci/kfad113.

DOI:10.1093/toxsci/kfad113
PMID:37941503
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10823772/
Abstract

Mechanistic toxicology seeks to identify the molecular and cellular mechanisms by which toxicants exert their deleterious effects. One powerful approach is to generate mutations in genes that respond to a particular toxicant, and then test how such mutations change the effects of the toxicant. CRISPR is a rapid and versatile approach to generate mutations in cultured cells and in animal models. Many studies use CRISPR to generate short insertions or deletions in a target gene and then assume that the resulting mutation, such as a premature termination codon, causes a loss of functional protein. However, recent studies demonstrate that this assumption is flawed. Cells can compensate for short insertion and deletion mutations, leading toxicologists to draw erroneous conclusions from mutant studies. In this review, we will discuss mechanisms by which a mutation in one gene may be rescued by compensatory activity. We will discuss how CRISPR insertion and deletion mutations are susceptible to compensation by transcriptional adaptation, alternative splicing, and rescue by maternally derived gene products. We will review evidence that measuring levels of messenger RNA transcribed from a mutated gene is an unreliable indicator of the severity of the mutation. Finally, we provide guidelines for using CRISPR to generate mutations that avoid compensation.

摘要

机制毒理学旨在确定毒物产生有害作用的分子和细胞机制。一种有效的方法是在对特定毒物有反应的基因中产生突变,然后测试这些突变如何改变毒物的作用。CRISPR是一种在培养细胞和动物模型中快速且通用的产生突变的方法。许多研究使用CRISPR在靶基因中产生短插入或缺失,然后假定产生的突变,如过早终止密码子,会导致功能性蛋白质的丧失。然而,最近的研究表明这一假设存在缺陷。细胞可以补偿短插入和缺失突变,导致毒理学家从突变研究中得出错误结论。在这篇综述中,我们将讨论一个基因中的突变可以通过补偿活性得以挽救的机制。我们将讨论CRISPR插入和缺失突变如何容易受到转录适应、可变剪接的补偿以及母源基因产物的挽救。我们将回顾证据表明,测量从突变基因转录的信使RNA水平是突变严重程度的不可靠指标。最后,我们提供了使用CRISPR产生避免补偿的突变的指导原则。