Centromeric Transcription Regulates Aurora-B Localization and Activation

Cell Rep. 2016 May 24;15(8):1624-33. doi: 10.1016/j.celrep.2016.04.054. Epub 2016 May 12.

Abstract

Centromeric transcription is widely conserved; however, it is not clear what role centromere transcription plays during mitosis. Here, I find that centromeres are transcribed in Xenopus egg extracts into a long noncoding RNA (lncRNA; cen-RNA) that localizes to mitotic centromeres, chromatin, and spindles. cen-RNAs bind to the chromosomal passenger complex (CPC) in vitro and in vivo. Blocking transcription or antisense inhibition of cen-RNA leads to a reduction of CPC localization to the inner centromere and misregulation of CPC component Aurora-B activation independently of known centromere recruitment pathways. Additionally, transcription is required for normal bipolar attachment of kinetochores to the mitotic spindle, consistent with a role for cen-RNA in CPC regulation. This work demonstrates that cen-RNAs promote normal kinetochore function through regulation of the localization and activation of the CPC and confirm that lncRNAs are components of the centromere.

MeSH terms

  • Animals
  • Aurora Kinase B / metabolism*
  • Cell Extracts
  • Centromere / genetics*
  • Centromere / metabolism
  • Chromatin / metabolism
  • Enzyme Activation
  • Kinetochores / metabolism
  • Microtubules / metabolism
  • Ovum / metabolism
  • Protein Transport
  • RNA / metabolism
  • RNA, Antisense / metabolism
  • Transcription, Genetic*
  • Xenopus laevis

Substances

  • Cell Extracts
  • Chromatin
  • RNA, Antisense
  • RNA
  • Aurora Kinase B