Kim Yonghwan, Tian Ming
Section of Molecular Genetics and Microbiology, University of Texas at Austin, 1 University Station, Austin, TX 78712, USA.
Mol Immunol. 2009 Oct;46(16):3283-91. doi: 10.1016/j.molimm.2009.07.027. Epub 2009 Aug 21.
Activation-induced cytidine deaminase (AID) is critical for immunoglobulin (Ig) diversification in B cells. The majority of evidence supports the model that AID modifies Ig genes at the DNA level by deaminating cytosines into uracils. The mutagenic activity is largely restricted to Ig genes to avoid genomic damage in general, but the underlying mechanism is not understood. We addressed this question in chicken B cell line DT40. We characterized a regulatory region within the Iglambda locus. This regulatory region is important for AID-mediated gene conversion at the Iglambda locus, and is capable of targeting AID activity to ectopic loci. This regulatory region contains binding sites for transcription factors NF-kappaB, Mef2 and octamer binding proteins. Mutation of these binding sites or ablation of NF-kappaB family member, p50 or c-Rel, impairs the AID targeting function of this regulatory region. These results suggest that NF-kappaB family of transcription factors contribute to AID-mediated gene conversion.
活化诱导的胞苷脱氨酶(AID)对于B细胞中免疫球蛋白(Ig)的多样化至关重要。大多数证据支持这样的模型:AID通过将胞嘧啶脱氨基为尿嘧啶在DNA水平上修饰Ig基因。为避免总体上的基因组损伤,这种诱变活性在很大程度上局限于Ig基因,但潜在机制尚不清楚。我们在鸡B细胞系DT40中解决了这个问题。我们鉴定了Iglambda基因座内的一个调控区域。该调控区域对于Iglambda基因座处AID介导的基因转换很重要,并且能够将AID活性靶向异位基因座。该调控区域包含转录因子NF-κB、Mef2和八聚体结合蛋白的结合位点。这些结合位点的突变或NF-κB家族成员p50或c-Rel的缺失会损害该调控区域的AID靶向功能。这些结果表明转录因子NF-κB家族有助于AID介导的基因转换。