生物
科尔1
质粒
底漆(化妆品)
复制的起源
RNA聚合酶
遗传学
分子生物学
核苷酸
DNA聚合酶Ⅰ
DNA复制
聚合酶
核糖核酸
DNA
逆转录酶
基因
有机化学
化学
作者
Gerald Selzer,Tapan Som,Tateo Itoh,Jun-ichi Tomizawa
出处
期刊:Cell
[Cell Press]
日期:1983-01-01
卷期号:32 (1): 119-129
被引量:205
标识
DOI:10.1016/0092-8674(83)90502-0
摘要
Replication of Escherichia coli plasmid p15A was examined by use of a cell extract or a mixture of three purified E. coli enzymes: RNA polymerase; RNAase H; and DNA polymerase I. In each system, replication initiates at any of three consecutive nucleotides located at a unique site. Primer transcription starts 508 bp upstream of the replication origin. The region between 294 and 524 bp upstream of the origin determines the incompatibility property. This region specifies an RNA (RNA I) of about 105 nucleotides that is involved in regulation of primer formation. We compare the nucleotide sequences around the origins of related plasmids p15A, ColE1, pBR322, RSF1030 and CloDF13, and discuss the significance of possible RNA secondary structures in primer formation.
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