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腺病毒2型感染期间由RNA聚合酶III转录的低分子量病毒RNA。

Low molecular weight viral RNAs transcribed by RNA polymerase III during adenovirus 2 infection.

作者信息

Weinmann R, Brendler T G, Raskas H J, Roeder R G

出版信息

Cell. 1976 Apr;7(4):557-66. doi: 10.1016/0092-8674(76)90206-3.

Abstract

Nuclei isolated from human cells productively infected with adenovirus 2 have been shown to synthesize four low molecular weight RNA species which hybridize efficiently to viral DNA. One species corresponds to the 5.5S or VA RNA (Ohe, Weissman, and Cooke, 1969), and is designated V156. The other three species are novel and have been designated V200, V140, V130, since they are approximately 200, 140, and 130 nucleotides in length, respectively. These viral RNAs retain their distinct electrophoretic properties after denaturation with formamide. RNA species with electrophoretic mobilities similar to those of the V200, V156, and V140 RNAs have been found in the cytoplasmic fraction of cells at late times after adenovirus infection. In isolated nuclei, the V200, V156, V140, and V130 RNAs are all synthesized by DNA-dependent RNA polymerase III, since synthesis is sensitive to high but not to low concentrations of alpha-amanitin. The synthesis of these low molecular weight RNAs continues for a prolonged period of time in isolated nuclei, suggesting that reinitiation occurs. Adenovirus 2 DNA fragments obtained by digestion with restriction endonucleases Eco RI and Sma I were used to map the location of the DNA sequences which encode the RNAs. All the low molecular weight RNAs hybridized to a region of the genome between o.18 and 0.38 fractional lengths from the left end of the adenovirus genome, suggesting that the respective DNA sequences are clustered. Other nonviral low molecular weight RNAs are synthesized in nuclei isolated from infected cells. These include the cellular 5S rRNA species which was minitored by its hybridization to purified 5S DNA from Xenopus laevis.

摘要

已证明,从被腺病毒2有效感染的人细胞中分离出的细胞核能合成四种低分子量RNA,它们能与病毒DNA高效杂交。其中一种与5.5S或VA RNA相对应(Ohe、Weissman和Cooke,1969),被命名为V156。另外三种是新发现的,分别命名为V200、V140、V130,因为它们的长度分别约为200、140和130个核苷酸。用甲酰胺变性后,这些病毒RNA仍保持其独特的电泳特性。在腺病毒感染后的晚期,在细胞的细胞质部分发现了电泳迁移率与V200、V156和V140 RNA相似的RNA。在分离的细胞核中,V200、V156、V140和V130 RNA均由依赖DNA的RNA聚合酶III合成,因为其合成对高浓度但不对低浓度的α-鹅膏蕈碱敏感。这些低分子量RNA在分离的细胞核中持续合成很长一段时间,表明发生了重新起始。用限制性内切酶Eco RI和Sma I消化获得的腺病毒2 DNA片段用于绘制编码这些RNA的DNA序列的位置。所有低分子量RNA都与腺病毒基因组左端0.18至0.38长度分数之间的基因组区域杂交,表明各自的DNA序列是成簇的。在从感染细胞中分离出的细胞核中还合成了其他非病毒低分子量RNA。其中包括细胞5S rRNA,通过其与非洲爪蟾纯化的5S DNA杂交进行监测。

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