Kapitonov Vladimir V, Koonin Eugene V
National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, USA.
Biol Direct. 2015 Apr 28;10:20. doi: 10.1186/s13062-015-0055-8.
The RAG1 and RAG2 proteins are essential subunits of the V(D)J recombinase that is required for the generation of the enormous variability of antibodies and T-cell receptors in jawed vertebrates. It was demonstrated previously that the 600-aa catalytic core of RAG1 evolved from the transposase of the Transib superfamily transposons. However, although homologs of RAG1 and RAG2 genes are adjacent in the purple sea urchin genome, a transposon encoding both proteins so far has not been reported. Here we describe such transposons in the genomes of green sea urchin, a starfish and an oyster. Comparison of the domain architectures of the RAG1 homologs in these transposons, denoted TransibSU, and other Transib superfamily transposases provides for reconstruction of the structure of the hypothetical TransibVDJ transposon that gave rise to the VDJ recombinases at the onset of vertebrate evolution some 500 million years ago.
RAG1和RAG2蛋白是V(D)J重组酶的必需亚基,而V(D)J重组酶是有颌脊椎动物产生抗体和T细胞受体巨大变异性所必需的。先前已证明,RAG1的600个氨基酸的催化核心是从Transib超家族转座子的转座酶进化而来的。然而,尽管RAG1和RAG2基因的同源物在紫海胆基因组中相邻,但迄今为止尚未报道编码这两种蛋白的转座子。在此,我们描述了绿海胆、一种海星和一种牡蛎基因组中的此类转座子。对这些转座子(称为TransibSU)中RAG1同源物的结构域结构与其他Transib超家族转座酶进行比较,有助于重建大约5亿年前脊椎动物进化开始时产生VDJ重组酶的假想TransibVDJ转座子的结构。