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Tracing the path of DNA substrates in active Tetrahymena telomerase holoenzyme complexes: mapping of DNA contact sites in the RNA subunit

机译:追踪活性四膜虫端粒酶全酶复合物中DNA底物的路径:绘制RNA亚基中DNA接触位点的图谱

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Telomerase, the enzyme that extends single-stranded telomeric DNA, consists of an RNA subunit (TER) including a short template sequence, a catalytic protein (TERT) and accessory proteins. We used site-specific UV cross-linking to map the binding sites for DNA primers in TER within active Tetrahymena telomerase holoenzyme complexes. The mapping was performed at single-nucleotide resolution by a novel technique based on RNase H digestion of RNA–DNA hybrids made with overlapping complementary oligodeoxynucleotides. These data allowed tracing of the DNA path through the telomerase complexes from the template to the TERT binding element (TBE) region of TER. TBE is known to bind TERT and to be involved in the template 5′-boundary definition. Based on these findings, we propose that upstream sequences of each growing telomeric DNA chain are involved in regulation of its growth arrest at the 5′-end of the RNA template. The upstream DNA–TBE interaction may also function as an anchor for the subsequent realignment of the 3′-end of the DNA with the 3′-end of the template to enable initiation of synthesis of a new telomeric repeat.
机译:端粒酶是一种延伸单链端粒DNA的酶,它由一个RNA亚基(TER)组成,包括一个短模板序列,一个催化蛋白(TERT)和辅助蛋白。我们使用位点特异性UV交联来绘制活性四膜虫端粒酶全酶复合物中TER中DNA引物的结合位点。通过基于重叠重叠互补寡聚脱氧核苷酸制成的RNA-DNA杂合体的RNase H消化的新技术,以单核苷酸分辨率进行了定位。这些数据允许通过端粒酶复合物从模板到TER的TERT结合元件(TBE)区域追踪DNA路径。已知TBE结合TERT并参与模板5'-边界的定义。基于这些发现,我们建议每个正在生长的端粒DNA链的上游序列都参与其在RNA模板5'端的生长停滞的调节。上游DNA-TBE相互作用也可以充当锚,随后将DNA的3'-末端与模板的3'-末端重新排列,以启动新端粒重复序列的合成。

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