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大肠杆菌复制起点oriC在体外和体内的局部DNA解链及结构扰动

Localized DNA melting and structural pertubations in the origin of replication, oriC, of Escherichia coli in vitro and in vivo.

作者信息

Gille H, Messer W

机构信息

Max-Planck-Institut für Immunbiologie, Spemann Laboratories, Freiburg, FRG.

出版信息

EMBO J. 1991 Jun;10(6):1579-84. doi: 10.1002/j.1460-2075.1991.tb07678.x.

Abstract

The leftmost region of the Escherichia coli origin of DNA replication (oriC) contains three tandemly repeated AT-rich 13mers which have been shown to become single-stranded during the early stages of initiation in vitro. Melting is induced by the ATP form of DnaA, the initiator protein of DNA replication. KMnO4 was used to probe for single-stranded regions and altered DNA conformation during the initiation of DNA replication at oriC in vitro and in vivo. Unpairing in the AT-rich 13mer region is thermodynamically stable even in the absence of DnaA protein, but only when divalent cations are omitted from the reaction. In the presence of Mg2+, oriC melting is strictly DnaA dependent. The sensitive region is distinct from that detected in the absence of DnaA as it is located further to the left within the minimal origin. In addition, the DNA is severely distorted between the three 13mers and the IHF binding site in oriC. A change of conformation can also be observed during the initiation of DNA replication in vivo. This is the first in vivo evidence for a structural change at the 13mers during initiation complex formation.

摘要

大肠杆菌DNA复制起点(oriC)的最左端区域包含三个串联重复的富含AT的13聚体,研究表明,在体外起始的早期阶段,这些13聚体可变成单链。DNA复制起始蛋白DnaA的ATP形式可诱导解链。在体外和体内oriC处DNA复制起始过程中,利用高锰酸钾探测单链区域和改变的DNA构象。即使在没有DnaA蛋白的情况下,富含AT的13聚体区域的解链在热力学上也是稳定的,但前提是反应中省略二价阳离子。在Mg2+存在的情况下,oriC解链严格依赖于DnaA。敏感区域与在没有DnaA时检测到的区域不同,因为它位于最小起点内更靠左的位置。此外,oriC中三个13聚体与整合宿主因子(IHF)结合位点之间的DNA严重扭曲。在体内DNA复制起始过程中也可观察到构象变化。这是在起始复合物形成过程中13聚体发生结构变化的首个体内证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d93d/452823/420e7c16b26a/emboj00104-0271-a.jpg

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