The Causes and Consequences of Genetic Interactions (Epistasis).

IF 7.7 2区 生物学 Q1 GENETICS & HEREDITY Annual review of genomics and human genetics Pub Date : 2019-08-31 Epub Date: 2019-05-13 DOI:10.1146/annurev-genom-083118-014857
Júlia Domingo, Pablo Baeza-Centurion, Ben Lehner
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引用次数: 138

Abstract

The same mutation can have different effects in different individuals. One important reason for this is that the outcome of a mutation can depend on the genetic context in which it occurs. This dependency is known as epistasis. In recent years, there has been a concerted effort to quantify the extent of pairwise and higher-order genetic interactions between mutations through deep mutagenesis of proteins and RNAs. This research has revealed two major components of epistasis: nonspecific genetic interactions caused by nonlinearities in genotype-to-phenotype maps, and specific interactions between particular mutations. Here, we provide an overview of our current understanding of the mechanisms causing epistasis at the molecular level, the consequences of genetic interactions for evolution and genetic prediction, and the applications of epistasis for understanding biology and determining macromolecular structures.

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遗传相互作用的原因和结果(上位性)。
同样的突变对不同的个体可能有不同的影响。其中一个重要的原因是,突变的结果可能取决于它发生的遗传环境。这种依赖性被称为上位性。近年来,通过蛋白质和rna的深度诱变,人们一直在努力量化突变之间的成对和高阶遗传相互作用的程度。本研究揭示了上位性的两个主要组成部分:由基因型-表型图谱非线性引起的非特异性遗传相互作用,以及特定突变之间的特异性相互作用。在这里,我们概述了目前在分子水平上引起上位性的机制,遗传相互作用对进化和遗传预测的影响,以及上位性在理解生物学和确定大分子结构方面的应用。
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来源期刊
CiteScore
14.90
自引率
1.10%
发文量
29
期刊介绍: Since its inception in 2000, the Annual Review of Genomics and Human Genetics has been dedicated to showcasing significant developments in genomics as they pertain to human genetics and the human genome. The journal emphasizes genomic technology, genome structure and function, genetic modification, human variation and population genetics, human evolution, and various aspects of human genetic diseases, including individualized medicine.
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