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Interaction between the phage HK022 Nun protein and the nut RNA of phage lambda.

机译:噬菌体HK022 Nun蛋白与噬菌体λ的螺母RNA之间的相互作用。

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摘要

The nun gene product of prophage HK022 excludes phage lambda infection by blocking the expression of genes downstream from the lambda nut sequence. The Nun protein functions both by competing with lambda N transcription-antitermination protein and by actively inducing transcription termination on the lambda chromosome. We demonstrate that Nun binds directly to a stem-loop structure within nut RNA, boxB, which is also the target for the N antiterminator. The two proteins show comparable affinities for boxB and they compete with each other. Their interactions with boxB are similar, as shown by RNase protection experiments, NMR spectroscopy, and analysis of boxB mutants. Each protein binds the 5' strand of the boxB stem and the adjacent loop. The stem does not melt upon the binding of Nun or N, as the 3' strand remains sensitive to a double-strand-specific RNase. The binding of RNA partially protects Nun from proteolysis and changes its NMR spectra. Evidently, although Nun and N bind to the same surface of boxB RNA, their respective complexes interact differently with RNA polymerase, inducing transcription termination or antitermination, respectively.
机译:噬菌体HK022的修女基因产物通过阻断λ螺母序列下游的基因表达来排除噬菌体λ感染。 Nun蛋白通过与λN转录-抗终止蛋白竞争并通过主动诱导λ染色体上的转录终止而起作用。我们证明Nun直接绑定到螺母RNA boxB内的茎环结构,boxB也是N抗终止剂的目标。这两种蛋白质对boxB具有相似的亲和力,并且彼此竞争。它们与boxB的相互作用相似,如RNase保护实验,NMR光谱和boxB突变体分析所示。每种蛋白质都与boxB茎的5'链和相邻环结合。由于3'链对双链特异性RNase敏感,因此茎在结合Nun或N时不会融化。 RNA的结合部分保护Nun免受蛋白水解并改变其NMR光谱。显然,尽管Nun和N与boxB RNA的同一表面结合,但它们各自的复合物与RNA聚合酶的相互作用不同,分别诱导转录终止或抗终止作用。

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