Mutational analysis of all conserved basic amino acids in RAG-1 reveals catalytic, step arrest, and joining-deficient mutants in the V(D)J recombinase

L. E. Huye, M. M. Purugganan, M. M. Jiang, D. B. Roth

Research output: Contribution to journalArticle

Abstract

Although both RAG-1 and RAG-2 are required for all steps of V(D)J recombination, little is known about the specific contribution of either protein to these steps. RAG-1 contains three acidic active-site amino acids that are thought to coordinate catalytic metal ions. To search for additional catalytic amino acids and to better define the functional anatomy of RAG-1, we mutated all 86 conserved basic amino acids to alanine and evaluated the mutant proteins for DNA binding, nicking, hairpin formation, and joining. We found several amino acids outside of the canonical nonamer-binding domain that are critical for DNA binding, several step arrest mutants with defects in nicking or hairpin formation, and four RAG-1 mutants defective specifically for joining. Analysis of coding joints formed by some of these mutants revealed excessive deletions, frequent use of short sequence homologies, and unusually long palindromic junctional inserts, known as P nucleotides, that result from aberrant hairpin opening. These features characterize junctions found in scid mice, which are deficient for the catalytic subunit of DNA-dependent protein kinase (DNA-PKcs), suggesting that the RAG proteins and DNA-PKcs perform overlapping functions in coding joint formation. Interestingly, the amino acids that are altered in 12 of our mutants are also mutated in human inherited immunodeficiency syndromes. Our analysis of these mutants provides insights into the molecular mechanisms underlying these disorders.
Original languageUndefined
Pages (from-to)3460-73
JournalMolecular and Cellular Biology
Volume22
Issue number10
StatePublished - 2002

Keywords

  • Alanine/metabolism Amino Acid Sequence Amino Acids/*metabolism Animals DNA/metabolism DNA Nucleotidyltransferases/chemistry/*genetics/metabolism DNA-Binding Proteins/genetics/metabolism Genes, RAG-1 Homeodomain Proteins/chemistry/*genetics/metabolism Humans Mice Molecular Sequence Data Mutagenesis, Site-Directed Mutation Nucleic Acid Conformation Oligonucleotides/metabolism Protein Structure, Tertiary Recombinant Fusion Proteins/metabolism Recombination, Genetic/*genetics Transposases/chemistry/genetics/metabolism VDJ Recombinases

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