Linker Histone H1.2 Directs Genome-wide Chromatin Association of the Retinoblastoma Tumor Suppressor Protein and Facilitates Its Function

Cell Rep. 2017 Jun 13;19(11):2193-2201. doi: 10.1016/j.celrep.2017.05.053.

Abstract

The retinoblastoma tumor suppressor protein pRb is a master regulator of cellular proliferation, principally through interaction with E2F and regulation of E2F target genes. Here, we describe the H1.2 linker histone as a major pRb interaction partner. We establish that H1.2 and pRb are found in a chromatin-bound complex on diverse E2F target genes. Interrogating the global influence of H1.2 on the genome-wide distribution of pRb indicated that the E2F target genes affected by H1.2 are functionally linked to cell-cycle control, consistent with the ability of H1.2 to hinder cell proliferation and the elevated levels of chromatin-bound H1-pRb complex, which occur in growth-arrested cells. Our results define a network of E2F target genes as susceptible to the regulatory influence of H1.2, where H1.2 augments global association of pRb with chromatin, enhances transcriptional repression by pRb, and facilitates pRb-dependent cell-cycle arrest.

Keywords: E2F; cell cycle; chromatin; linker histone; retinoblastoma protein; transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle Checkpoints
  • Chromatin / genetics*
  • Genes, Tumor Suppressor / physiology*
  • Histones / genetics*
  • Humans
  • Retinoblastoma / genetics*
  • Retinoblastoma Protein / metabolism*
  • Transfection

Substances

  • Chromatin
  • Histones
  • Retinoblastoma Protein