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Interaction between antibody-diversification enzyme AID and spliceosome-associated factor CTNNBL1.
Conticello, Silvestro G; Ganesh, Karuna; Xue, Kanmin; Lu, Mason; Rada, Cristina; Neuberger, Michael S.
Affiliation
  • Conticello SG; Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK. Electronic address: silvo.conticello@ittumori.it.
  • Ganesh K; Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK.
  • Xue K; Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK.
  • Lu M; Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK.
  • Rada C; Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK.
  • Neuberger MS; Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK. Electronic address: msn@mrc-lmb.cam.ac.uk.
Mol Cell ; 31(4): 474-484, 2008 Aug 22.
Article in En | MEDLINE | ID: mdl-18722174
ABSTRACT
Activation-induced deaminase (AID) deaminates deoxycytidine residues in immunoglobulin genes, triggering antibody diversification. Here, by use of two-hybrid and coimmunoprecipitation assays, we identify CTNNBL1 (also known as NAP) as an AID-specific interactor. Mutants of AID that interfere with CTNNBL1 interaction yield severely diminished hypermutation and class switching. Targeted inactivation of CTNNBL1 in DT40 B cells also considerably diminishes IgV diversification. CTNNBL1 is a widely expressed nuclear protein that associates with the Prp19 complex of the spliceosome, interacting with its CDC5L component. The results, therefore, identify residues in AID involved in its in vivo targeting and suggest they might act through interaction with CTNNBL1, giving possible insight into the linkage between AID recruitment and target-gene transcription.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Nuclear Proteins / Spliceosomes / Cytidine Deaminase / Apoptosis Regulatory Proteins / Antibody Diversity Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals / Humans Language: En Journal: Mol Cell Journal subject: BIOLOGIA MOLECULAR Year: 2008 Type: Article

Full text: 1 Database: MEDLINE Main subject: Nuclear Proteins / Spliceosomes / Cytidine Deaminase / Apoptosis Regulatory Proteins / Antibody Diversity Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals / Humans Language: En Journal: Mol Cell Journal subject: BIOLOGIA MOLECULAR Year: 2008 Type: Article