1. Academic Validation
  2. Activation induced cytidine deaminase mutant (AID-His130Pro) from Hyper IgM 2 patient retained mutagenic activity on SHM artificial substrate

Activation induced cytidine deaminase mutant (AID-His130Pro) from Hyper IgM 2 patient retained mutagenic activity on SHM artificial substrate

  • Mol Immunol. 2016 Nov;79:77-82. doi: 10.1016/j.molimm.2016.09.025.
Hanen Ouadani 1 Imen Ben-Mustapha 1 Meriem Ben-Ali 1 Beya Larguèche 2 Tihana Jovanic 3 Sylvie Garcia 4 Benoit Arcangioli 5 Houda Elloumi-Zghal 2 Dahmani Fathallah 2 Mongia Hachicha 6 Hatem Masmoudi 7 François Rougeon 3 Mohamed-Ridha Barbouche 8
Affiliations

Affiliations

  • 1 Laboratory of Transmission, Control and Immunobiology of Infection (LR11IPT02), Institut Pasteur de Tunis, Tunisia; University Tunis El Manar, Tunis, Tunisia.
  • 2 Laboratory of Transmission, Control and Immunobiology of Infection (LR11IPT02), Institut Pasteur de Tunis, Tunisia.
  • 3 Biochemistry and Genetics Development Unit (URA CNRS 2581), Institut Pasteur Paris, France.
  • 4 Laboratory of Lymphocyte Population Biology, Institut Pasteur Paris, France.
  • 5 Laboratory of Dynamics of the Genome, Institut Pasteur, France.
  • 6 Department of Pediatrics, Hedi Chaker Hospital, Sfax, Tunisia.
  • 7 Laboratory of Immunology, Habib Bourguiba Hospital, Sfax, Tunisia.
  • 8 Laboratory of Transmission, Control and Immunobiology of Infection (LR11IPT02), Institut Pasteur de Tunis, Tunisia; University Tunis El Manar, Tunis, Tunisia. Electronic address: [email protected].
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.

Keywords

AID mutagenic activity; Activation induced cytidine deaminase; Class switch recombination; Cofactors; Hyper IgM 2; Somatic hypermutation.

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