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首页> 外文期刊>Journal of Molecular Biology >Reverse Transcriptase and Reverse Splicing Activities Encoded by the Mobile Group II Intron COBI1 of Fission Yeast Mitochondrial DNA.
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Reverse Transcriptase and Reverse Splicing Activities Encoded by the Mobile Group II Intron COBI1 of Fission Yeast Mitochondrial DNA.

机译:裂变酵母线粒体DNA的Mobile II组内含子COBI1编码的逆转录酶和反向剪接活性。

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摘要

Mobile group II introns encode multidomain proteins with maturase activity involved in splicing and reverse transcriptase (RT) and (often) endonuclease activities involved in intron mobility. These activities are present in a ribonucleoprotein complex that contains the excised intron RNA and the intron-encoded protein. Here, we report biochemical studies of the protein encoded by the group IIA1 intron in the cob gene of fission yeast Schizosaccharomyces pombe mitochondria (cobI1). RNP particle fractions from the wild-type fission yeast strain with cobI1 in its mtDNA have RT activity even without adding an exogenous primer. Characterization of the cDNA products of such reactions showed a strong preference for excised intron RNA as template. Two main regions for initiation of cDNA synthesis were mapped within the intron, one near the DIVa putative high-affinity binding site for the intron-encoded protein and the other near domain VI. Adding exogenous primers complementary to cob exon 2 sequences near theintron/exon boundary stimulated RT activity but mainly for pre-mRNA rather than mRNA templates. Further in vitro experiments demonstrated that cobI1 RNA in RNP particle fractions can reverse splice into double-stranded DNA substrates containing the intron homing site. Target DNA primed reverse transcription was not detected unless a DNA target was used that was already nicked in the antisense strand of exon 2. This study shows that S.pombe cobI1 encodes RNP particles that have most of the biochemical activities needed for it to be a retroelement. Interestingly, it appears to lack an endonuclease activity, suggesting that the active homing exhibited by this intron in crosses may differ somewhat from that of the better-characterized introns.
机译:流动的II组内含子编码具有参与剪接的成熟酶活性和涉及内含子迁移性的逆转录酶(RT)和(通常)核酸内切酶活性的多域蛋白。这些活性存在于核糖核蛋白复合物中,该复合物包含已切除的内含子RNA和内含子编码的蛋白。在这里,我们报告由裂变酵母粟酒裂殖酵母线粒体(cobI1)的cob基因中的IIA1内含子组编码的蛋白质的生化研究。来自野生型裂变酵母菌株的mtDNA中具有cobI1的RNP颗粒级分即使不添加外源引物也具有RT活性。此类反应的cDNA产物的表征显示,强烈倾向于将内含子RNA作为模板。内含子内有两个主要的cDNA合成起始区域,一个位于内含子编码蛋白的DIVa推定的高亲和力结合位点附近,另一个位于域VI附近。在内含子/外显子边界附近添加与cob外显子2序列互补的外源引物可刺激RT活性,但主要用于前mRNA而非mRNA模板。进一步的体外实验表明,RNP颗粒级分中的cobI1 RNA可以反向剪接成包含内含子归巢位点的双链DNA底物。除非使用已在外显子2的反义链中刻痕的DNA靶,否则无法检测到靶DNA引发的逆转录。这项研究表明,S.pombe cobI1编码具有其必需的大部分生化活性的RNP颗粒。改造。有趣的是,它似乎缺乏核酸内切酶活性,表明该内含子在杂交中表现出的主动归巢可能与特性更好的内含子有所不同。

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