Ubiquitylation of RAG-2 by Skp2-SCF links destruction of the V(D)J recombinase to the cell cycle

Mol Cell. 2005 Jun 10;18(6):699-709. doi: 10.1016/j.molcel.2005.05.011.

Abstract

The periodic destruction of RAG-2 at the G1-to-S transition couples V(D)J recombination to the G0 and G1 cell cycle phases and coordinates RAG-mediated DNA cleavage with DNA repair by nonhomologous end joining. To define the mechanism by which this occurs, we reproduced cell cycle-dependent regulation of the V(D)J recombinase in a cell-free system. The ubiquitin-proteasomal pathway carries out destruction of RAG-2 in lysates of S phase cells and during S phase in vivo. Remarkably, the Skp2-SCF ubiquitin ligase, which plays a central role in cell cycle regulation through the destruction of p27, mediates ubiquitylation of RAG-2 in vitro and degradation of RAG-2 in vivo. The regulation of antigen receptor gene assembly by Skp2-SCF provides an unexpected and direct mechanistic link between DNA recombination and the cell cycle.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell Cycle / physiology*
  • DNA-Binding Proteins / metabolism*
  • G1 Phase
  • HeLa Cells
  • Humans
  • Nuclear Proteins
  • Recombination, Genetic
  • S Phase
  • S-Phase Kinase-Associated Proteins / metabolism*
  • Ubiquitin / metabolism*
  • VDJ Recombinases / metabolism*

Substances

  • DNA-Binding Proteins
  • Nuclear Proteins
  • RAG2 protein, human
  • S-Phase Kinase-Associated Proteins
  • Ubiquitin
  • V(D)J recombination activating protein 2
  • VDJ Recombinases