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Repair of DNA double-strand breaks in Escherichia coli cells requires synthesis of proteins that can be induced by UV light.

机译:修复大肠杆菌细胞中DNA双链断裂需要合成可以被紫外线诱导的蛋白质。

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摘要

The repair of DNA double-strand breaks in Escherichia coli cells irradiated with gamma rays occurs only after new proteins are synthesized in response to damage introduced in the genome DNA. One protein whose synthesis is thus induced is the recA protein, and previous work has shown that recA- cells do not repair double-strand breaks. However, inducing recA protein by treating cells with nalidixic acid does not induce repair of double-strand breaks, so this repair requires more than the presence of the recA protein. When repair of double-strand breaks is blocked, the genome DNA is degraded by an endonuclease-like action. Evidence is presented to show that the inducible inhibition of DNA degradation after x-irradiation [Pollard, E. C. & Randall, E. P. (1973) Radiat. Res. 55, 265] is probably caused by the inducible repair of DNA double-strand breaks.
机译:伽马射线辐照的大肠杆菌细胞中DNA双链断裂的修复仅在响应于基因组DNA中引入的损伤而合成新蛋白质后才发生。因此诱导合成的一种蛋白质是recA蛋白,先前的研究表明recA细胞不能修复双链断裂。但是,通过用萘啶酸处理细胞来诱导recA蛋白不会诱导双链断裂的修复,因此这种修复比recA蛋白的存在还需要更多。当双链断裂的修复被阻断时,基因组DNA被内切核酸酶样作用降解。提出的证据表明,X-射线辐照后DNA降解的诱导抑制作用[Pollard,E.C。和Randall,E.P。(1973)Radiat.Acad.Sci.USA。 Res。 [55,265]可能是由DNA双链断裂的诱导修复引起的。

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  • 作者

    Krasin, F; Hutchinson, F;

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  • 年度 1981
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  • 正文语种 en
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