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      Genomic and Biochemical Insights into the Specificity of ETS Transcription Factors

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          Abstract

          ETS proteins are a group of evolutionarily related, DNA-binding transcriptional factors. These proteins direct gene expression in diverse normal and disease states by binding to specific promoters and enhancers and facilitating assembly of other components of the transcriptional machinery. The highly conserved DNA-binding ETS domain defines the family and is responsible for specific recognition of a common sequence motif, 5′-GGA(A/T)-3′. Attaining specificity for biological regulation in such a family is thus a conundrum. We present the current knowledge of routes to functional diversity and DNA binding specificity, including divergent properties of the conserved ETS and PNT domains, the involvement of flanking structured and unstructured regions appended to these dynamic domains, posttranslational modifications, and protein partnerships with other DNA-binding proteins and coregulators. The review emphasizes recent advances from biochemical and biophysical approaches, as well as insights from genomic studies that detect ETS-factor occupancy in living cells.

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          Author and article information

          Journal
          2985150R
          665
          Annu Rev Biochem
          Annu. Rev. Biochem.
          Annual review of biochemistry
          0066-4154
          1545-4509
          13 July 2017
          2011
          23 August 2017
          : 80
          : 437-471
          Affiliations
          [1 ]Medical Sciences, Indiana University School of Medicine, Bloomington, Indiana 47405
          [2 ]Department of Biochemistry and Molecular Biology, Department of Chemistry, and The Michael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3
          [3 ]Department of Oncological Sciences, Huntsman Cancer Institute, University of Utah Health Sciences, Salt Lake City, Utah 84112
          [4 ]Howard Hughes Medical Institute, Chevy Chase, Maryland 20815
          Article
          PMC5568663 PMC5568663 5568663 nihpa892069
          10.1146/annurev.biochem.79.081507.103945
          5568663
          21548782
          5784ea05-d6c6-41ef-9bdf-ca50ee040531
          History
          Categories
          Article

          ChIP-Seq,protein dynamics,PNT domain,ETS domain,DNA binding,autoinhibition

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