| Literature DB >> 27716525 |
Hanen Ouadani1, Imen Ben-Mustapha1, Meriem Ben-Ali1, Beya Larguèche2, Tihana Jovanic3, Sylvie Garcia4, Benoit Arcangioli5, Houda Elloumi-Zghal2, Dahmani Fathallah2, Mongia Hachicha6, Hatem Masmoudi7, François Rougeon3, Mohamed-Ridha Barbouche8.
Abstract
Activation induced cytidine deaminase (AID) is an essential enzyme for class switch recombination (CSR) and somatic hypermutation (SHM) during secondary immune response. Mutations in the AICDA gene are responsible for Hyper IgM 2 syndrome where both CSR and SHM or only CSR are affected. Indeed, triggering either of the two mechanisms requires the DNA deamination activity of AID. Besides, different domains of AID may be differentially involved in CSR and SHM through their interaction with specific cofactors. Herein, we studied the AID-induced SHM activity of the AID-His130Pro mutant identified in a patient with Hyper IgM 2 syndrome. AID mutagenic activity was monitored by the reversion of nonsense mutations of the EGFP gene assessed by flow cytometry. We found that the His130Pro mutation, which affects CSR, preserves AID mutagenic activity. Indeed, the His130 residue is located in a putative specific CSR region in the APOBEC-like domain, known to involve CSR specific cofactors that probably play a major role in AID physiological activities. Copyright ÂEntities:
Keywords: AID mutagenic activity; Activation induced cytidine deaminase; Class switch recombination; Cofactors; Hyper IgM 2; Somatic hypermutation
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Year: 2016 PMID: 27716525 DOI: 10.1016/j.molimm.2016.09.025
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407