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Cis-regulatory mutations with driver hallmarks in major cancers.


ABSTRACT: Despite the recent availability of complete genome sequences of tumors from thousands of patients, isolating disease-causing (driver) non-coding mutations from the plethora of somatic variants remains challenging, and only a handful of validated examples exist. By integrating whole-genome sequencing, genetic data, and allele-specific gene expression from TCGA, we identified 320 somatic non-coding mutations that affect gene expression in cis (FDR<0.25). These mutations cluster into 47 cis-regulatory elements that modulate expression of their subject genes through diverse molecular mechanisms. We further show that these mutations have hallmark features of non-coding drivers; namely, that they preferentially disrupt transcription factor binding motifs, are associated with a selective advantage, increased oncogene expression and decreased tumor suppressor expression.

SUBMITTER: Cheng Z 

PROVIDER: S-EPMC7903341 | biostudies-literature | 2021 Mar

REPOSITORIES: biostudies-literature

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<i>Cis-</i>regulatory mutations with driver hallmarks in major cancers.

Cheng Zhongshan Z   Vermeulen Michael M   Rollins-Green Micheal M   DeVeale Brian B   Babak Tomas T  

iScience 20210204 3


Despite the recent availability of complete genome sequences of tumors from thousands of patients, isolating disease-causing (driver) non-coding mutations from the plethora of somatic variants remains challenging, and only a handful of validated examples exist. By integrating whole-genome sequencing, genetic data, and allele-specific gene expression from TCGA, we identified 320 somatic non-coding mutations that affect gene expression in <i>cis</i> (FDR<0.25). These mutations cluster into 47 cis-  ...[more]

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