Thompson Blaine K, Christensen Shawn M
Department of Biology; University of Texas at Arlington; Arlington, TX USA.
Mob Genet Elements. 2011 May;1(1):29-37. doi: 10.4161/mge.1.1.16485.
Restriction-like endonuclease (RLE) bearing non-LTR retrotransposons are site-specific elements that integrate into the genome through a target primed reverse transcription mechanism (TPRT). R2 elements have been used as a model system for investigating non-LTR retrotransposon integration. We previously demonstrated that R2 retrotransposons require two subunits of the element-encoded multifunctional protein to integrate-one subunit bound upstream of the insertion site and one bound downstream. R2 elements have been phylogenetically categorized into four clades: R2-A, B, C and D, that diverged from a common ancestor more than 850 million years ago. All R2 elements target the same sequence within 28S rDNA. The amino-terminal domain of R2Bm, an R2-D clade element, contains a single zinc finger and a Myb motif that are responsible for binding R2 protein downstream of the insertion site. Target site recognition is of interest as it is the first step in the integration reaction and may help elucidate evolutionary history and integration mechanism. The amino-terminal domain of R2-A clade members contains three zinc fingers and a Myb motif. We show here that R2Lp, an R2-A clade member, uses its amino-terminal DNA binding motifs to bind upstream of the insertion site. Because the R2-A and R2-D clade elements recognize 28S rDNA differently, we conclude the A- and D-clades represent independent targeting events to the 28S site. Our results also indicate a certain plasticity of insertional mechanics exists between the two clades.
携带非长末端重复反转录转座子的类限制内切酶(RLE)是通过靶标引发逆转录机制(TPRT)整合到基因组中的位点特异性元件。R2元件已被用作研究非长末端重复反转录转座子整合的模型系统。我们之前证明,R2反转录转座子需要元件编码的多功能蛋白的两个亚基才能进行整合——一个亚基结合在插入位点上游,另一个结合在下游。R2元件在系统发育上已被分为四个进化枝:R2-A、B、C和D,它们在8.5亿多年前从一个共同祖先分化而来。所有R2元件都靶向28S rDNA内的相同序列。R2-D进化枝元件R2Bm的氨基末端结构域包含一个单一的锌指和一个Myb基序,它们负责在插入位点下游结合R2蛋白。靶位点识别很重要,因为它是整合反应的第一步,可能有助于阐明进化历史和整合机制。R2-A进化枝成员的氨基末端结构域包含三个锌指和一个Myb基序。我们在此表明,R2-A进化枝成员R2Lp利用其氨基末端DNA结合基序在插入位点上游结合。由于R2-A和R2-D进化枝元件对28S rDNA的识别方式不同,我们得出结论,A进化枝和D进化枝代表了对28S位点的独立靶向事件。我们的结果还表明,这两个进化枝之间存在一定的插入机制可塑性。