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在染色体复制叉通过后,大肠杆菌oriC和dnaA基因启动子会与DNA腺嘌呤甲基转移酶隔离。

E. coli oriC and the dnaA gene promoter are sequestered from dam methyltransferase following the passage of the chromosomal replication fork.

作者信息

Campbell J L, Kleckner N

机构信息

Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.

出版信息

Cell. 1990 Sep 7;62(5):967-79. doi: 10.1016/0092-8674(90)90271-f.

Abstract

We have examined individual GATC sites throughout the E. coli genome for their kinetics of remethylation by dam methyltransferase following the passage of the chromosomal replication fork. We present evidence for three major conclusions: that oriC is a single function unit that is specifically sequestered from dam methyltransferase for a significant period of time and then released; that the dnaA promoter region is subject to sequestration analogous to that observed at oriC and thus that hemimethylation-dependent sequestration is a general phenomenon; and that each round of replication initiation triggers a transient, temporally coordinate block in both reinitiation at oriC and expression of the dnaA gene. These and other observations are all consistent with the notion that hemimethylation in these two regions acts coordinately to ensure that every origin undergoes initiation once and only once per cell cycle; other possible roles for sequestration at dnaA are also considered.

摘要

我们研究了大肠杆菌基因组中各个GATC位点在染色体复制叉通过后被dam甲基转移酶重新甲基化的动力学。我们提供了三个主要结论的证据:oriC是一个单一功能单元,在相当长的一段时间内被特异性地隔离于dam甲基转移酶之外,然后被释放;dnaA启动子区域经历类似于在oriC观察到的隔离,因此半甲基化依赖性隔离是一种普遍现象;并且每一轮复制起始都会在oriC的重新起始和dnaA基因的表达中触发一个短暂的、时间上协调的阻断。这些以及其他观察结果都与这样一种观点一致,即这两个区域的半甲基化协同作用,以确保每个复制起点在每个细胞周期中仅起始一次;还考虑了在dnaA处隔离的其他可能作用。

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