Amino acid residues in Rag1 crucial for DNA hairpin formation

Catherine P Lu, Hector Sandoval, Vicky L Brandt, Phoebe A Rice, David B Roth

Research output: Contribution to journalArticle

31 Scopus citations

Abstract

The Rag proteins carry out V(D)J recombination through a process mechanistically similar to cut-and-paste transposition. Specifically, Rag complexes form DNA hairpins through direct transesterification, using a catalytic Asp-Asp-Glu (DDE) triad in Rag1. How is sufficient DNA distortion introduced to allow hairpin formation? We hypothesized that, like certain transposases, the Rag proteins might use aromatic amino acid residues to stabilize a flipped-out base. Through in vivo and in vitro experiments and structural predictions, we identified residues in Rag1 crucial for hairpin formation. One of these, a conserved tryptophan (Trp893), probably participates in base-stacking interactions near the cleavage site, as do Trp298, Trp265 and Trp319 in the Tn5, Tn10 and Hermes transposases, respectively. Other residues surrounding the catalytic glutamate (YKEFRK) may share functional similarities with the YREK motif in IS4 family transposases.

Original languageEnglish (US)
Pages (from-to)1010-5
Number of pages6
JournalNature Structural and Molecular Biology
Volume13
Issue number11
DOIs
StatePublished - Nov 2006

Keywords

  • Amino Acid Sequence
  • Amino Acids, Aromatic
  • Animals
  • CHO Cells
  • Catalytic Domain
  • Conserved Sequence
  • Cricetinae
  • DNA
  • Homeodomain Proteins
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Nucleic Acid Conformation
  • Sequence Alignment
  • Structure-Activity Relationship
  • Transposases
  • VDJ Recombinases
  • Journal Article
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

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