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Mutations in the U5 Region Adjacent to the Primer Binding Site Affect tRNA Cleavage by Human Immunodeficiency Virus Type 1 Reverse Transcriptase In Vivo▿

机译:U5区中与引物结合位点相邻的突变影响人免疫缺陷病毒1型逆转录酶体内的tRNA切割

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摘要

In retroviruses, the first nucleotide added to the tRNA primer defines the end of the U5 region in the right long terminal repeat, and the subsequent removal of this tRNA primer by RNase H exactly defines the U5 end of the linear double-stranded DNA. In most retroviruses, the entire tRNA is removed by RNase H cleavage at the RNA/DNA junction. However, the RNase H domain of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase cleaves the tRNA 1 nucleotide from the RNA/DNA junction at the U5/primer binding site (PBS) junction, which leaves an rA residue at the U5 terminus. We made sequence changes at the end of the U5 region adjacent to the PBS in HIV-1 to determine whether such changes affect the specificity of tRNA primer cleavage by RNase H. In some of the mutants, RNase H usually removed the entire tRNA, showing that the cleavage specificity was shifted by 1 nucleotide. This result suggests that the tRNA cleavage specificity of the HIV-1 RNase domain H depends on sequences in U5.
机译:在逆转录病毒中,添加到tRNA引物中的第一个核苷酸定义了右长末端重复序列中U5区域的末端,随后被RNase H去除的tRNA引物恰好定义了线性双链DNA的U5末端。在大多数逆转录病毒中,整个tRNA通过RNA / DNA连接处的RNase H裂解而被去除。但是,人类免疫缺陷病毒1型(HIV-1)逆转录酶的RNase H结构域从U5 /引物结合位点(PBS)交界处的RNA / DNA交界处切割了tRNA 1核苷酸,从而在U5处留下了rA残基总站。我们在与HIV-1中的PBS相邻的U5区末端进行了序列改变,以确定这些改变是否影响RNase H切割tRNA引物的特异性。在某些突变体中,RNase H通常会去除整个tRNA,显示切割特异性移位了1个核苷酸。该结果表明HIV-1 RNase结构域H的tRNA切割特异性取决于U5中的序列。

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