Drosha regulates gene expression independently of RNA cleavage function

Cell Rep. 2013 Dec 26;5(6):1499-510. doi: 10.1016/j.celrep.2013.11.032. Epub 2013 Dec 19.

Abstract

Drosha is the main RNase III-like enzyme involved in the process of microRNA (miRNA) biogenesis in the nucleus. Using whole-genome ChIP-on-chip analysis, we demonstrate that, in addition to miRNA sequences, Drosha specifically binds promoter-proximal regions of many human genes in a transcription-dependent manner. This binding is not associated with miRNA production or RNA cleavage. Drosha knockdown in HeLa cells downregulated nascent gene transcription, resulting in a reduction of polyadenylated mRNA produced from these gene regions. Furthermore, we show that this function of Drosha is dependent on its N-terminal protein-interaction domain, which associates with the RNA-binding protein CBP80 and RNA Polymerase II. Consequently, we uncover a previously unsuspected RNA cleavage-independent function of Drosha in the regulation of human gene expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • HeLa Cells
  • Humans
  • MicroRNAs / metabolism*
  • Nuclear Cap-Binding Protein Complex / metabolism
  • Promoter Regions, Genetic
  • Protein Binding
  • RNA Polymerase II / metabolism
  • RNA Processing, Post-Transcriptional*
  • RNA Stability*
  • Ribonuclease III / chemistry
  • Ribonuclease III / genetics
  • Ribonuclease III / metabolism*
  • Transcription Elongation, Genetic*

Substances

  • MicroRNAs
  • Nuclear Cap-Binding Protein Complex
  • RNA Polymerase II
  • DROSHA protein, human
  • Ribonuclease III