The acetyllysine reader BRD3R promotes human nuclear reprogramming and regulates mitosis

Academic Article

Abstract

  • It is well known that both recipient cells and donor nuclei demonstrate a mitotic advantage as observed in the traditional reprogramming with somatic cell nuclear transfer (SCNT). However, it is not known whether a specific mitotic factor plays a critical role in reprogramming. Here we identify an isoform of human bromodomain-containing 3 (BRD3), BRD3R (BRD3 with Reprogramming activity), as a reprogramming factor. BRD3R positively regulates mitosis during reprogramming, upregulates a large set of mitotic genes at early stages of reprogramming, and associates with mitotic chromatin. Interestingly, a set of the mitotic genes upregulated by BRD3R constitutes a pluripotent molecular signature. The two BRD3 isoforms display differential binding to acetylated histones. Our results suggest a molecular interpretation for the mitotic advantage in reprogramming and show that mitosis may be a driving force of reprogramming.
  • Published In

    Digital Object Identifier (doi)

    Pubmed Id

  • 2983858
  • Author List

  • Shao Z; Zhang R; Khodadadi-Jamayran A; Chen B; Crowley MR; Festok MA; Crossman DK; Townes TM; Hu K
  • Volume

  • 7