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Article Dans Une Revue Journal of Experimental Medicine Année : 2008

Proteasomal degradation restricts the nuclear lifespan of AID.

Résumé

Activation-induced cytidine deaminase (AID) initiates all postrearrangement processes that diversify the immunoglobulin repertoire by specific deamination of cytidines at the immunoglobulin (Ig) locus. As uncontrolled expression of AID is potentially mutagenic, different types of regulation, particularly nucleocytoplasmic shuttling, restrict the likelihood of AID-deoxyribonucleic acid encounters. We studied additional mechanisms of regulation affecting the stability of the AID protein. No modulation of protein accumulation according to the cell cycle was observed in a Burkitt's lymphoma cell line. In contrast, the half-life of AID was markedly reduced in the nucleus, and this destabilization was accompanied by a polyubiquitination that was revealed in the presence of proteasome inhibitors. The same compartment-specific degradation was observed in activated mouse B cells, and also in a non-B cell line. No specific lysine residues could be linked to this degradation, so it remains unclear whether polyubiquitination proceeds through several alternatives sites or through the protein N terminus. The nuclear-restricted form of AID displayed enhanced mutagenicity at both Ig and non-Ig loci, most notably at TP53, suggesting that modulation of nuclear AID content through proteasomal degradation may represent another level of control of AID activity.

Domaines

Immunologie
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Dates et versions

inserm-00321674 , version 1 (15-09-2008)

Identifiants

Citer

Said Aoufouchi, Ahmad Faili, Carole Zober, Orietta d'Orlando, Sandra Weller, et al.. Proteasomal degradation restricts the nuclear lifespan of AID.. Journal of Experimental Medicine, 2008, 205 (6), pp.1357-68. ⟨10.1084/jem.20070950⟩. ⟨inserm-00321674⟩

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