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细胞膜组分对处于半甲基化状态的pBR322复制起点处DNA合成的抑制作用。

Inhibition of DNA synthesis at the hemimethylated pBR322 origin of replication by a cell membrane fraction.

作者信息

Malki A, Kern R, Kohiyama M, Hughes P

机构信息

Department of Molecular Biology, Institut Jacques Monod, Universite Paris VII, France.

出版信息

Nucleic Acids Res. 1992 Jan 11;20(1):105-9. doi: 10.1093/nar/20.1.105.

Abstract

The replication of both ColE1-type plasmids and plasmids bearing the origin of replication of the Escherichia coli chromosome (oriC) has been shown to be inhibited by hemimethylation of adenine residues within GATC sequences. In the case of oriC plasmids, this inhibition was previously shown to be mediated by the specific affinity of the hemimethylated origin DNA for an outer cell membrane fraction. Here, we suggest that a similar mechanism is operating in the case of the ColE1-like plasmid pBR322 as (i) a hemimethylated DNA fragment carrying the promoter for the RNA which primes DNA synthesis (RNAII) is specifically bound by the same membrane fraction and, (ii) the addition of the membrane fraction to a soluble assay of pBR322 replication results in preferential inhibition of initiation on the hemimethylated template. We suggest that membrane sequestration of hemimethylated origin DNA and/or associated replication genes following replication may be a common element restricting DNA replication to precise moments in the cell cycle.

摘要

研究表明,ColE1型质粒以及携带大肠杆菌染色体复制起点(oriC)的质粒的复制会受到GATC序列内腺嘌呤残基半甲基化的抑制。对于oriC质粒,先前已证明这种抑制作用是由半甲基化的起始DNA与外细胞膜组分的特异性亲和力介导的。在此,我们认为类似的机制也在ColE1样质粒pBR322中起作用,原因如下:(i)携带引发DNA合成的RNA(RNAII)启动子的半甲基化DNA片段会被相同的膜组分特异性结合;(ii)将膜组分添加到pBR322复制的可溶性检测体系中会优先抑制半甲基化模板上的起始过程。我们认为,复制后半甲基化起始DNA和/或相关复制基因的膜隔离可能是将DNA复制限制在细胞周期精确时刻的一个共同因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc50/310332/1ea27e0cefe9/nar00075-0121-a.jpg

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