The Genetics of Transcription Factor DNA Binding Variation

Bart Deplancke, Daniel Alpern, Vincent Gardeux

Research output: Contribution to journalReview article

86 Citations (Scopus)

Abstract

Most complex trait-associated variants are located in non-coding regulatory regions of the genome, where they have been shown to disrupt transcription factor (TF)-DNA binding motifs. Variable TF-DNA interactions are therefore increasingly considered as key drivers of phenotypic variation. However, recent genome-wide studies revealed that the majority of variable TF-DNA binding events are not driven by sequence alterations in the motif of the studied TF. This observation implies that the molecular mechanisms underlying TF-DNA binding variation and, by extrapolation, inter-individual phenotypic variation are more complex than originally anticipated. Here, we summarize the findings that led to this important paradigm shift and review proposed mechanisms for local, proximal, or distal genetic variation-driven variable TF-DNA binding. In addition, we discuss the biomedical implications of these findings for our ability to dissect the molecular role(s) of non-coding genetic variants in complex traits, including disease susceptibility.

Original languageEnglish (US)
Pages (from-to)538-554
Number of pages17
JournalCell
Volume166
Issue number3
DOIs
StatePublished - Jul 28 2016
Externally publishedYes

Fingerprint

Genetic Transcription
Transcription Factors
DNA
Genes
Genome
Nucleotide Motifs
Nucleic Acid Regulatory Sequences
Disease Susceptibility
Extrapolation
Genetics

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

The Genetics of Transcription Factor DNA Binding Variation. / Deplancke, Bart; Alpern, Daniel; Gardeux, Vincent.

In: Cell, Vol. 166, No. 3, 28.07.2016, p. 538-554.

Research output: Contribution to journalReview article

Deplancke, Bart ; Alpern, Daniel ; Gardeux, Vincent. / The Genetics of Transcription Factor DNA Binding Variation. In: Cell. 2016 ; Vol. 166, No. 3. pp. 538-554.
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