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Two deletions within genes for simian virus 40 structural proteins VP2 and VP3 lead to formation of abnormal transcriptional complexes.

机译:猿猴病毒40个结构蛋白VP2和VP3的基因内的两个缺失导致异常转录复合物的形成。

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摘要

The procedure developed by R. M. Fernandez-Muñoz et al. (J. Virol. 29:612-623, 1979) for isolating simian virus 40 (SV 40) chromatin free of disrupted previrions was optimized for preparing late transcriptional complexes, and these complexes were partially characterized. Transcriptional complexes derived from wild-type virus and from several deletion and temperature-sensitive mutants could be activated more than five-fold either by the anionic detergent Sarkosyl or by 300 mM ammonium sulfate, in agreement with the properties of SV40 transcriptional complexes prepared by other procedures. In contrast, complexes from cells infected with deletion mutants dl1261 or dl1262 were not activated at all by a high salt concentration, even though the extent of their activation by Sarkosyl was normal. Mutants dl1261 and dl1262 carry deletions of 54 and 36 base pairs, respectively, at an approximate map position of 0.91, which is within the overlapping genes for the virion proteins VP2 and VP3. The effects of these deletions on transcription in vitro indicate that VP2 or VP3 or both are bound to late transcriptional complexes in a way that affects the progress of initiated RNA polymerase. The properties of late transcriptional complexes derived from wild-type SV40 can be explained by the presence of the following two different kinds of complexes: (i) a minority class (about 20%), which is free of VP2 or VP3, active at low concentrations of ammonium sulfate in vitro, and responsible for late transcription in vivo, and (ii) a majority class (about 80%) with VP2 or VP3 bound, which is inactive at low salt concentrations both in vitro and in vivo but capable of being activated by high salt concentrations or by Sarkosyl. We propose that mutant VP2 and VP3 proteins from dl1261 and dl1262 bind to the majority class of late transcriptional complexes in a way that can be reversed by Sarkosyl but not by a high salt concentration.
机译:R. M.Fernandez-Muñoz等人开发的程序。 (J.Virol.29:612-623,1979)用于分离没有破坏的前病毒体的猿猴病毒40(SV 40)染色质被优化用于制备晚期转录复合物,并且对这些复合物进行了部分表征。可以通过阴离子洗涤剂Sarkosyl或300 mM硫酸铵将源自野生型病毒以及一些缺失和温度敏感突变体的转录复合物激活五倍以上,这与其他方法制备的SV40转录复合物的特性一致程序。相反,来自被缺失突变体dl1261或dl1262感染的细胞的复合物根本没有被高盐浓度活化,即使它们被Sarkosyl活化的程度是正常的。突变体dl1261和dl1262分别在约0.91的图谱位置带有54和36个碱基对的缺失,这在病毒体蛋白VP2和VP3的重叠基因内。这些缺失对体外转录的影响表明VP2或VP3或两者都以影响起始RNA聚合酶进程的方式与后期转录复合物结合。源自野生型SV40的后期转录复合物的特性可以通过以下两种不同类型的复合物的存在来解释:(i)少数类(约20%),不含VP2或VP3,在低浓度时具有活性浓度的硫酸铵在体外,并负责体内的后期转录;以及(ii)多数种类(约80%)的VP2或VP3结合物,在体外和体内低盐浓度下均无活性,但能够高盐浓度或Sarkosyl激活。我们提出,来自dl1261和dl1262的突变VP2和VP3蛋白以一种可以被Sarkosyl逆转但不能被高盐浓度逆转的方式与大多数后期转录复合物结合。

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