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

被引:8
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
相关论文
共 75 条
  • [51] Construction of hybrid regulated mother specific yeast promoters for inducible differential gene expression
    Pothoulakis, Georgios
    Ellis, Tom
    [J]. PLOS ONE, 2018, 13 (03):
  • [52] Network of epistatic interactions within a yeast snoRNA
    Puchta, Olga
    Cseke, Botond
    Czaja, Hubert
    Tollervey, David
    Sanguinetti, Guido
    Kudla, Grzegorz
    [J]. SCIENCE, 2016, 352 (6287) : 840 - 844
  • [53] Global epistasis emerges from a generic model of a complex trait
    Reddy, Gautam
    Desai, Michael M.
    [J]. ELIFE, 2021, 10
  • [54] Enhancing homology-directed genome editing by catalytically active and inactive CRISPR-Cas9 using asymmetric donor DNA
    Richardson, Christopher D.
    Ray, Graham J.
    DeWitt, Mark A.
    Curie, Gemma L.
    Corn, Jacob E.
    [J]. NATURE BIOTECHNOLOGY, 2016, 34 (03) : 339 - +
  • [55] From Peas to Disease: Modifier Genes, Network Resilience, and the Genetics of Health
    Riordan, Jesse D.
    Nadeau, Joseph H.
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2017, 101 (02) : 177 - 191
  • [56] The three yeast A kinases have specific signaling functions in pseudohyphal growth
    Robertson, LS
    Fink, GR
    [J]. 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
    Rockman, Matthew V.
    [J]. EVOLUTION, 2012, 66 (01) : 1 - 17
  • [58] PKA and Sch9 control a molecular switch important for the proper adaptation to nutrient availability
    Roosen, J
    Engelen, K
    Marchal, K
    Mathys, J
    Griffioen, G
    Cameroni, E
    Thevelein, JM
    De Virgilio, C
    De Moor, B
    Winderickx, J
    [J]. MOLECULAR MICROBIOLOGY, 2005, 55 (03) : 862 - 880
  • [59] Hsp90 as a capacitor for morphological evolution
    Rutherford, SL
    Lindquist, S
    [J]. NATURE, 1998, 396 (6709) : 336 - 342
  • [60] Genotypic Context and Epistasis in Individuals and Populations
    Sackton, Timothy B.
    Hartl, Daniel L.
    [J]. CELL, 2016, 166 (02) : 279 - 287