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通过电子显微镜对大肠杆菌RNA聚合酶结合位点在噬菌体S13和0X174 DNA上的定位

Localization of Escherichia coli RNA polymerase binding sites on bacteriophage S13 and 0X174 DNAs by electron microscopy.

作者信息

Rassart E, Spencer J H, Zollinger M

出版信息

J Virol. 1979 Jan;29(1):179-84. doi: 10.1128/JVI.29.1.179-184.1979.

Abstract

Complexes between Escherichia coli RNA polymerase and bacteriophage S13 and phage phiX174 replicative form III DNAs have been shown to form at specific locations on the phage genomes. The major locations on S13 have been mapped at 8 to 10 and 92 to 96% of the genome length, starting from the unique Pst I cleavage site. The locations correspond to the beginnings of genes D and B, respectively. Four minor locations map at 18 to 22, 28 to 32, 50 to 56, and 70 to 74% of the genome. The 70 to 74% site corresponds to the beginning of the A gene. The major locations on phiX174 are at 8 to 10, 50 to 54, and 92 to 94% of the genome. The 50 to 54% site is at the start of the H gene and has an equivalent minor site on S13, but it is not a promoter site. Three minor sites on phiX174, at 20 to 24, 26 to 32, and 68 to 74% of the genome, correspond to sites on S13. The data confirm the locations of sites identified by restriction fragment binding experiments (E. Rassart and J. H. Spencer, J. Virol. 27:677--687, 1978) and the assignment of putative promoters at the start of genes A, B and D.

摘要

已证明大肠杆菌RNA聚合酶与噬菌体S13及噬菌体φX174复制型III DNA之间的复合物在噬菌体基因组的特定位置形成。从独特的Pst I切割位点开始,S13上的主要位置已定位在基因组长度的8%至10%以及92%至96%处。这些位置分别对应基因D和B的起始处。四个次要位置分别位于基因组的18%至22%、28%至32%、50%至56%以及70%至74%处。70%至74%的位点对应基因A的起始处。φX174上的主要位置在基因组的8%至10%、50%至54%以及92%至94%处。50%至54%的位点位于H基因的起始处,在S13上有一个等效的次要位点,但它不是启动子位点。φX174上的三个次要位点,分别位于基因组的20%至24%、26%至32%以及68%至74%处,与S13上的位点相对应。这些数据证实了通过限制性片段结合实验所确定的位点位置(E. Rassart和J. H. Spencer,《病毒学杂志》27:677 - 687,1978年)以及在基因A、B和D起始处假定启动子的定位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee67/353096/1fcae48665ec/jvirol00181-0199-a.jpg

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