Widespread epistasis among beneficial genetic variants revealed by high-throughput genome editing

被引:12
作者
Ang, Roy Moh Lik [1 ]
Chen, Shi-An A. [2 ]
Kern, Alexander F. [1 ]
Xie, Yihua [2 ]
Fraser, Hunter B. [2 ]
机构
[1] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
来源
CELL GENOMICS | 2023年 / 3卷 / 04期
关键词
SACCHAROMYCES-CEREVISIAE; MODIFIER GENES; YEAST; EVOLUTION; PROTEIN; FLOCCULATION; ADAPTATION; EXPRESSION; MUTATIONS; PHENOTYPE;
D O I
10.1016/j.xgen.2023.100260
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The phenotypic effect of any genetic variant can be altered by variation at other genomic loci. Known as epistasis, these genetic interactions shape the genotype-phenotype map of every species, yet their origins remain poorly understood. To investigate this, we employed high-throughput genome editing to measure the fitness effects of 1,826 naturally polymorphic variants in four strains of Saccharomyces cerevisiae. About 31% of variants affect fitness, of which 24% have strain-specific fitness effects indicative of epistasis. We found that beneficial variants are more likely to exhibit genetic interactions and that these inter-actions can be mediated by specific traits such as flocculation ability. This work suggests that adaptive evolution will often involve trade-offs where a variant is only beneficial in some genetic backgrounds, potentially explaining why many beneficial variants remain polymorphic. In sum, we provide a framework to understand the factors influencing epistasis with single-nucleotide resolution, revealing widespread epistasis among beneficial variants.
引用
收藏
页数:24
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共 75 条
[51]   Construction of hybrid regulated mother specific yeast promoters for inducible differential gene expression [J].
Pothoulakis, Georgios ;
Ellis, Tom .
PLOS ONE, 2018, 13 (03)
[52]   Network of epistatic interactions within a yeast snoRNA [J].
Puchta, Olga ;
Cseke, Botond ;
Czaja, Hubert ;
Tollervey, David ;
Sanguinetti, Guido ;
Kudla, Grzegorz .
SCIENCE, 2016, 352 (6287) :840-844
[53]   Global epistasis emerges from a generic model of a complex trait [J].
Reddy, Gautam ;
Desai, Michael M. .
ELIFE, 2021, 10
[54]   Enhancing homology-directed genome editing by catalytically active and inactive CRISPR-Cas9 using asymmetric donor DNA [J].
Richardson, Christopher D. ;
Ray, Graham J. ;
DeWitt, Mark A. ;
Curie, Gemma L. ;
Corn, Jacob E. .
NATURE BIOTECHNOLOGY, 2016, 34 (03) :339-+
[55]   From Peas to Disease: Modifier Genes, Network Resilience, and the Genetics of Health [J].
Riordan, Jesse D. ;
Nadeau, Joseph H. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2017, 101 (02) :177-191
[56]   The three yeast A kinases have specific signaling functions in pseudohyphal growth [J].
Robertson, LS ;
Fink, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (23) :13783-13787
[57]   THE QTN PROGRAM AND THE ALLELES THAT MATTER FOR EVOLUTION: ALL THAT'S GOLD DOES NOT GLITTER [J].
Rockman, Matthew V. .
EVOLUTION, 2012, 66 (01) :1-17
[58]   PKA and Sch9 control a molecular switch important for the proper adaptation to nutrient availability [J].
Roosen, J ;
Engelen, K ;
Marchal, K ;
Mathys, J ;
Griffioen, G ;
Cameroni, E ;
Thevelein, JM ;
De Virgilio, C ;
De Moor, B ;
Winderickx, J .
MOLECULAR MICROBIOLOGY, 2005, 55 (03) :862-880
[59]   Hsp90 as a capacitor for morphological evolution [J].
Rutherford, SL ;
Lindquist, S .
NATURE, 1998, 396 (6709) :336-342
[60]   Genotypic Context and Epistasis in Individuals and Populations [J].
Sackton, Timothy B. ;
Hartl, Daniel L. .
CELL, 2016, 166 (02) :279-287