首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Origin-specific DNA-binding membrane-associated protein may be involved in repression of initiation of DNA replication in Bacillus subtilis.
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Origin-specific DNA-binding membrane-associated protein may be involved in repression of initiation of DNA replication in Bacillus subtilis.

机译:特定于起源的DNA结合膜相关蛋白可能与抑制枯草芽孢杆菌中DNA复制的启动有关。

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摘要

Previous binding studies with labeled double-stranded Bacillus subtilis DNA fragments to a protein blot of renatured Bacillus membrane proteins showed selective binding of two adjacent origin fragments to a 64-kDa protein. The selective binding of the 64-kDa protein could be blocked by prior incubation of the blots with a specific polyclonal antibody. An in vitro replication system derived from a B. subtilis DNA-membrane complex showed initiation activity without addition of exogenous enzymes or template. When the complex was first incubated with the 64-kDa antibody or with its Fab fragments, initiation activity was enhanced. Antibodies to several other Bacillus membrane proteins as well as nonspecific antibodies did not show any significant stimulatory effect. A heavy-density-label experiment indicated that the complex initiated multiple rounds of replication in the presence of the 64-kDa antibody but not in its absence. The 64-kDa antibody plus an initiation inhibitor (streptovaricin) showed only repair and elongation activity. The 64-kDa protein may act in vivo as a repressor/regulator of initiation activity.
机译:先前用标记的双链枯草芽孢杆菌DNA片段与变性的芽孢杆菌膜蛋白的蛋白质印迹进行的结合研究表明,两个相邻的起始片段与64 kDa蛋白选择性结合。可以通过事先将印迹与特异性多克隆抗体一起孵育来阻止64 kDa蛋白的选择性结合。源自枯草芽孢杆菌DNA-膜复合物的体外复制系统显示出起始活性,而没有添加外源酶或模板。当复合物首先与64-kDa抗体或其Fab片段一起孵育时,启动活性得到增强。针对其他几种芽孢杆菌膜蛋白的抗体以及非特异性抗体均未显示任何明显的刺激作用。一项高密度标记实验表明,该复合物在存在64 kDa抗体的情况下启动了多轮复制,但在不存在抗体的情况下却未启动。 64 kDa抗体加起始抑制剂(链霉菌素)仅显示修复和延长活性。 64-kDa蛋白可在体内充当起始活性的阻遏物/调节物。

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