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酵母DNA由同源RNA聚合酶I和II进行转录:核糖体基因由RNA聚合酶I进行选择性转录。

Transcription of yeast DNA by homologous RNA polymerases I and II: selective transcription of ribosomal genes by RNA polymerase I.

作者信息

Holland M J, Hager G L, Rutter W J

出版信息

Biochemistry. 1977 Jan 11;16(1):16-24. doi: 10.1021/bi00620a003.

Abstract

Purified yeast DNA was transcribed by homologous RNA polymerases I and II and Escherichia coli RNA polymerase. Transcripts synthesized in vitro were analyzed by molecular hybridization with complementary DNA (cDNA) synthesized from yeast poly(A)-containing mRNA with viral reverse transcriptase and ribosomal DNA labeled in vitro by nick translation with E. coli DNA polymerase I. RNA synthesized by polymerase I and II in the presence of Mn2+ contained sequences complementary to cDNA and rDNA at a frequency consistent with random transcription of the template. Similarly, E. coli RNA polymerase synthesized an apparently random transcript in the presence of either Mn2+ or Mg2+. In contrast to these results, RNA polymerase I but not polymerase II transcripts were markedly enriched in sequences complementary to rDNA when transcription was carried out in the presence of Mg2+. The observed enrichment was 15-30-fold higher than observed for polymerase II or E. coli polymerase transcripts and is consistent with the transcript being comprised of 6-10% ribosomal sequences. These data strongly suggest that RNA polymerase I plays a critical role in selective transcription of ribosomal cistrons.

摘要

纯化的酵母DNA由同源的RNA聚合酶I和II以及大肠杆菌RNA聚合酶进行转录。体外合成的转录本通过与用病毒逆转录酶从含酵母多聚腺苷酸(poly(A))的mRNA合成的互补DNA(cDNA)进行分子杂交分析,以及通过用大肠杆菌DNA聚合酶I缺口平移法体外标记的核糖体DNA进行分析。在锰离子(Mn2+)存在下,由聚合酶I和II合成的RNA含有与cDNA和rDNA互补的序列,其频率与模板的随机转录一致。同样,大肠杆菌RNA聚合酶在Mn2+或镁离子(Mg2+)存在下合成了一个明显随机的转录本。与这些结果相反,当在Mg2+存在下进行转录时,RNA聚合酶I而非聚合酶II的转录本在与rDNA互补的序列中显著富集。观察到的富集程度比聚合酶II或大肠杆菌聚合酶转录本高15 - 30倍,并且与转录本由6 - 10%的核糖体序列组成一致。这些数据强烈表明RNA聚合酶I在核糖体顺反子的选择性转录中起关键作用。

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