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Meta-analysis of Chromatin Programming by Steroid Receptors

  • Ville Paakinaho
  • , Erin E. Swinstead
  • , Diego M. Presman
  • , Lars Grøntved
  • , Gordon L. Hager*
  • *Kontaktforfatter
  • University of Eastern Finland
  • National Cancer Institute
  • University of Buenos Aires

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

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Abstract

Transcription factors (TFs) must access chromatin to bind to their response elements and regulate gene expression. A widely accepted model proposes that only a special subset of TFs, pioneer factors, can associate with condensed chromatin and initiate chromatin opening. We previously reported that steroid receptors (SRs), not considered pioneer factors, can assist the binding of an archetypal pioneer, the forkhead box protein 1 (FOXA1), at a subset of receptor-activated enhancers. These findings have been challenged recently, with the suggestion that newly acquired data fully support the prevailing pioneer model. Here, we reexamine our results and confirm the original conclusions. We also analyze and discuss a number of available datasets relevant to chromatin penetration by SRs and find a general consensus supporting our original observations. Hence, we propose that chromatin opening at some sites can be initiated by SRs, with a parallel recruitment of factors often treated as having a unique pioneer function. This Matters Arising paper is in response to Glont et al. (2019), published in Cell Reports.

OriginalsprogEngelsk
TidsskriftCell Reports
Vol/bind28
Udgave nummer13
Sider (fra-til)3523-3534
Antal sider15
ISSN2211-1247
DOI
StatusUdgivet - 24. sep. 2019

Finansiering

V.P. was supported by the Academy of Finland and the Sigrid Jusélius Foundation . E.E.S. was supported by the Office of the Assistant Secretary of Defense for Health Affairs through the Breast Cancer Research Program under award W81XWH-17-1-0067 . Opinions, interpretations, conclusions, and recommendations are those of the author and are not necessarily endorsed by the Department of Defense. D.M.P. was supported by CONICET and the ANPCyT ( PICT 2017-0850 ). L.G. was supported by the Independent Research Fund Denmark and the Danish National Research Foundation . G.L.H. was supported by the Intramural Research Program of the CCR, NCI, NIH .

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