Inhibition of mRNA deadenylation by the nuclear cap binding complex (CBC)

J Biol Chem. 2006 Feb 17;281(7):4517-22. doi: 10.1074/jbc.M508590200. Epub 2005 Nov 28.

Abstract

Poly(A)-specific ribonuclease (PARN) is a cap-interacting and poly(A)-specific 3'-exoribonuclease. Here we have investigated how the cap binding complex (CBC) affects human PARN activity. We showed that CBC, via its 80-kDa subunit (CBP80), inhibited PARN, suggesting that CBC can regulate mRNA deadenylation. The CBC-mediated inhibition of PARN was cap-independent, and in keeping with this, the CBP80 subunit alone inhibited PARN. Our data suggested a new function for CBC, identified CBC as a potential regulator of PARN, and emphasized the importance of communication between the two extreme ends of the mRNA as a key strategy to regulate mRNA degradation. Based on our data, we have proposed a model for CBC-mediated regulation of PARN, which relies on an interaction between CBP80 and PARN. Association of CBC with PARN might have importance in the regulated recruitment of PARN to the nonsense-mediated decay pathway during the pioneer round of translation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Exoribonucleases / antagonists & inhibitors*
  • Exoribonucleases / physiology
  • Humans
  • Nuclear Cap-Binding Protein Complex / physiology*
  • Polyadenylation
  • Protein Subunits
  • RNA Caps / physiology
  • RNA, Messenger / metabolism*

Substances

  • Nuclear Cap-Binding Protein Complex
  • Protein Subunits
  • RNA Caps
  • RNA, Messenger
  • Exoribonucleases
  • poly(A)-specific ribonuclease