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Altered pattern of immunoglobulin hypermutation in mice deficient in Slip-GC protein.

We recently identified a novel germinal center GTPase, SLIP-GC, that localizes to replication factories in B cells and that, when reduced, induces DNA breaks in lymphoma B cell lines in an activation-induced deaminase (AID)-dependent manner. Herein, we generated mice deficient in SLIP-GC and examined the impact of SLIP-GC deficiency in immunoglobulin hypermutation and class switch recombination, both AID-dependent mechanisms. SLIP-GC-deficient mice experienced a substantial increase in mutations at G:C base pairs at the region downstream of JH4 in the immunoglobulin heavy chain locus. This change was reflected in the overall mutation frequency, and it was associated with an increase in transitions from G:C base pairs, a hallmark of AID-mediated deamination during replication. In addition, G:C transitions at non-immunoglobulin loci also increased in these mice. Given the intracellular localization of SLIP-GC to sites of replicating DNA, these results suggest that SLIP-GC protects replicating DNA from AID-mediated deamination of cytosines in both strands.

Pubmed ID: 22833677 RIS Download

Mesh terms: Animals | B-Lymphocytes | Cytidine Deaminase | Cytosine | DNA Mutational Analysis | DNA Replication | GTP Phosphohydrolases | Genotype | Germinal Center | Immunoglobulin Class Switching | Immunoglobulins | Lymphocyte Activation | Mice | Mice, Inbred C57BL | Mice, Knockout | Models, Genetic | Peyer's Patches | Somatic Hypermutation, Immunoglobulin

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Associated grants

  • Agency: NIEHS NIH HHS, Id: Z01 ES101603
  • Agency: Intramural NIH HHS, Id:

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