Department of Immunobiology, College of Medicine, University of Arizona, Tucson, AZ 85724, USA.
Dev Comp Immunol. 2012 May;37(1):176-83. doi: 10.1016/j.dci.2011.08.018. Epub 2011 Sep 8.
In a recent publication we demonstrated that somatic hypermutation occurs in the V region of the TCR γ gene of the sandbar shark (Carcharhinus plumbeus). We hypothesize that similar mechanisms are used to generate somatic mutations in both immunoglobulin and TCR γ genes of the sharks. Two distinct patterns of mutation occur, single nucleotide mutations (point mutations) and mutations comprising 2-5 consecutive bases (tandem mutations). Our data indicates that point mutations occur by a mechanism similar to that of somatic hypermutation in immunoglobulin genes of mammals, whereas tandem mutations may be generated by an error-prone DNA polymerase with terminal deoxynucleotidyl transferase (TdT)-like activity. Shark hotspot motifs identical to those of higher vertebrates were identified. We confirm that, as in immunoglobulin of sharks and higher vertebrates, highly significant targeting of AID activity to the classical DGYW/WRCH motif occurs in somatic hypermutation of sandbar shark TCR γ V genes. Our analysis suggests that the purpose of somatic mutations in shark TCR γ V-regions is to generate a more diverse repertoire in γ/δ receptors, rather than receptors with higher affinity.
在最近的一篇出版物中,我们证明了沙虎鲨(Carcharhinus plumbeus)的 TCR γ 基因的 V 区发生体细胞超突变。我们假设鲨鱼的免疫球蛋白和 TCR γ 基因中使用类似的机制来产生体细胞突变。发生两种不同类型的突变模式,单核苷酸突变(点突变)和包含 2-5 个连续碱基的突变(串联突变)。我们的数据表明,点突变是通过类似于哺乳动物免疫球蛋白基因中的体细胞超突变的机制发生的,而串联突变可能是由具有末端脱氧核苷酸转移酶(TdT)样活性的易错 DNA 聚合酶产生的。鉴定到与高等脊椎动物相同的鲨鱼热点基序。我们证实,与鲨鱼和高等脊椎动物的免疫球蛋白一样,AID 活性对经典的 DGYW/WRCH 基序的高度靶向发生在沙虎鲨 TCR γ V 基因的体细胞超突变中。我们的分析表明,鲨鱼 TCR γ V 区体细胞突变的目的是在 γ/δ 受体中产生更具多样性的库,而不是具有更高亲和力的受体。