Role of RAG1 autoubiquitination in V(D)J recombination

Proc Natl Acad Sci U S A. 2015 Jul 14;112(28):8579-83. doi: 10.1073/pnas.1510464112. Epub 2015 Jun 29.

Abstract

The variable domains of Ig and T-cell receptor genes in vertebrates are assembled from gene fragments by the V(D)J recombination process. The RAG1-RAG2 recombinase (RAG1/2) initiates this recombination by cutting DNA at the borders of recombination signal sequences (RSS) and their neighboring gene segments. The RAG1 protein is also known to contain a ubiquitin E3 ligase activity, located in an N-terminal region that is not strictly required for the basic recombination reaction but helps to regulate recombination. The isolated E3 ligase domain was earlier shown to ubiquitinate one site in a neighboring RAG1 sequence. Here we show that autoubiquitination of full-length RAG1 at this specific residue (K233) results in a large increase of DNA cleavage by RAG1/2. A mutational block of the ubiquitination site abolishes this effect and inhibits recombination of a test substrate in mouse cells. Thus, ubiquitination of RAG1, which can be promoted by RAG1's own ubiquitin ligase activity, plays a significant role in governing the level of V(D)J recombination activity.

Keywords: diversification; immunoglobulin; ubiquitin.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • DNA Cleavage
  • Homeodomain Proteins / metabolism*
  • Mice
  • Ubiquitination*
  • V(D)J Recombination*

Substances

  • Homeodomain Proteins
  • RAG-1 protein