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首页> 外文期刊>Nucleic acids research >Yeast RNA polymerase I binds preferentially to A+T-rich linkers in rDNA
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Yeast RNA polymerase I binds preferentially to A+T-rich linkers in rDNA

机译:酵母RNA聚合酶I优先结合到RDNA中的+ T-富含的接头

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Restriction fragments of yeast rDNA retained by purified RNA polymerases on nitrocellulose filters were analysed by gel eleotrophoresis. The EcoRI fragment B was preferentially retained by RNA polymerise I, but not by RNA polymerase III. The in vivo initiation sites for both polymerases are located within this fragment. Further analysis indicated that the preferred binding site for RNA polymerase I is highly AT-rich regions rather than a true promoter. The reported selective in vitro transcription of rDNA by purified yeast RNA polymerase I could then be explained by this preferential binding.
机译:通过凝胶Eleootrophoreris分析通过纯化的RNA聚合酶保留在硝酸纤维素过滤器上保留的酵母RDNA的限制片段。 ECORI片段B优先由RNA聚合I保留,但不是由RNA聚合酶III保留。两种聚合酶的体内起始位点位于该片段内。进一步的分析表明,RNA聚合酶I的优选结合位点I具有高度富有的区域,而不是真正的启动子。通过纯化的酵母RNA聚合酶I,通过纯化的酵母RNA聚合酶I可以解释所报道的rDNA的体外转录。

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