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Functional Genetic Variants Revealed by Massively Parallel Precise Genome Editing.


ABSTRACT: A major challenge in genetics is to identify genetic variants driving natural phenotypic variation. However, current methods of genetic mapping have limited resolution. To address this challenge, we developed a CRISPR-Cas9-based high-throughput genome editing approach that can introduce thousands of specific genetic variants in a single experiment. This enabled us to study the fitness consequences of 16,006 natural genetic variants in yeast. We identified 572 variants with significant fitness differences in glucose media; these are highly enriched in promoters, particularly in transcription factor binding sites, while only 19.2% affect amino acid sequences. Strikingly, nearby variants nearly always favor the same parent's alleles, suggesting that lineage-specific selection is often driven by multiple clustered variants. In sum, our genome editing approach reveals the genetic architecture of fitness variation at single-base resolution and could be adapted to measure the effects of genome-wide genetic variation in any screen for cell survival or cell-sortable markers.

SUBMITTER: Sharon E 

PROVIDER: S-EPMC6563827 | biostudies-literature | 2018 Oct

REPOSITORIES: biostudies-literature

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Functional Genetic Variants Revealed by Massively Parallel Precise Genome Editing.

Sharon Eilon E   Chen Shi-An A SA   Khosla Neil M NM   Smith Justin D JD   Pritchard Jonathan K JK   Fraser Hunter B HB  

Cell 20180920 2


A major challenge in genetics is to identify genetic variants driving natural phenotypic variation. However, current methods of genetic mapping have limited resolution. To address this challenge, we developed a CRISPR-Cas9-based high-throughput genome editing approach that can introduce thousands of specific genetic variants in a single experiment. This enabled us to study the fitness consequences of 16,006 natural genetic variants in yeast. We identified 572 variants with significant fitness di  ...[more]

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