Conticello Silvestro G, Thomas Cornelia J F, Petersen-Mahrt Svend K, Neuberger Michael S
Medical Research Council Laboratory of Molecular Biology, Cambridge, UK.
Mol Biol Evol. 2005 Feb;22(2):367-77. doi: 10.1093/molbev/msi026. Epub 2004 Oct 20.
The AID/APOBEC family (comprising AID, APOBEC1, APOBEC2, and APOBEC3 subgroups) contains members that can deaminate cytidine in RNA and/or DNA and exhibit diverse physiological functions (AID and APOBEC3 deaminating DNA to trigger pathways in adaptive and innate immunity; APOBEC1 mediating apolipoprotein B RNA editing). The founder member APOBEC1, which has been used as a paradigm, is an RNA-editing enzyme with proposed antecedents in yeast. Here, we have undertaken phylogenetic analysis to glean insight into the primary physiological function of the AID/APOBEC family. We find that although the family forms part of a larger superfamily of deaminases distributed throughout the biological world, the AID/APOBEC family itself is restricted to vertebrates with homologs of AID (a DNA deaminase that triggers antibody gene diversification) and of APOBEC2 (unknown function) identifiable in sequence databases from bony fish, birds, amphibians, and mammals. The cloning of an AID homolog from dogfish reveals that AID extends at least as far back as cartilaginous fish. Like mammalian AID, the pufferfish AID homolog can trigger deoxycytidine deamination in DNA but, consistent with its cold-blooded origin, is thermolabile. The fine specificity of its mutator activity and the biased codon usage in pufferfish IgV genes appear broadly similar to that of their mammalian counterparts, consistent with a coevolution of the antibody mutator and its substrate for the optimal targeting of somatic mutation during antibody maturation. By contrast, APOBEC1 and APOBEC3 are later evolutionary arrivals with orthologs not found in pufferfish (although synteny with mammals is maintained in respect of the flanking loci). We conclude that AID and APOBEC2 are likely to be the ancestral members of the AID/APOBEC family (going back to the beginning of vertebrate speciation) with both APOBEC1 and APOBEC3 being mammal-specific derivatives of AID and a complex set of domain shuffling underpinning the expansion and evolution of the primate APOBEC3s.
AID/APOBEC家族(包括AID、APOBEC1、APOBEC2和APOBEC3亚组)包含能够使RNA和/或DNA中的胞嘧啶脱氨基并展现出多种生理功能的成员(AID和APOBEC3使DNA脱氨基以触发适应性免疫和先天性免疫途径;APOBEC1介导载脂蛋白B的RNA编辑)。该家族的创始成员APOBEC1一直被用作范例,它是一种RNA编辑酶,在酵母中可能有其前身。在这里,我们进行了系统发育分析,以深入了解AID/APOBEC家族的主要生理功能。我们发现,尽管该家族是分布于整个生物界的一个更大的脱氨酶超家族的一部分,但AID/APOBEC家族本身仅限于脊椎动物,在硬骨鱼、鸟类、两栖动物和哺乳动物的序列数据库中可识别出AID(一种触发抗体基因多样化的DNA脱氨酶)和APOBEC2(功能未知)的同源物。从角鲨中克隆出的AID同源物表明,AID至少可追溯到软骨鱼。与哺乳动物的AID一样,河豚的AID同源物能够触发DNA中的脱氧胞嘧啶脱氨基,但与其冷血起源一致,它对热不稳定。其诱变活性的精细特异性以及河豚IgV基因中偏向的密码子使用情况,与其哺乳动物对应物大致相似,这与抗体成熟过程中抗体诱变剂及其底物为实现体细胞突变的最佳靶向而共同进化相一致。相比之下,APOBEC1和APOBEC3是后来进化出现的,在河豚中未发现直系同源物(尽管侧翼基因座与哺乳动物保持着共线性)。我们得出结论,AID和APOBEC2可能是AID/APOBEC家族的祖先成员(可追溯到脊椎动物物种形成之初),APOBEC1和APOBEC3都是AID的哺乳动物特异性衍生物,并且一系列复杂的结构域重排支撑了灵长类动物APOBEC3的扩展和进化。