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对来自猴疱疹病毒基因组中致癌所需区域转录的RNA进行图谱绘制。

Mapping of RNA transcribed from a region of the Herpesvirus saimiri genome required for oncogenicity.

作者信息

Kamine J, Bakker A, Desrosiers R C

出版信息

J Virol. 1984 Nov;52(2):532-40. doi: 10.1128/JVI.52.2.532-540.1984.

Abstract

A region of the Herpesvirus saimiri genome that is not essential for replication of the virus has recently been shown to be required for its oncogenicity in New World primates. We have examined the RNAs derived from this region of the genome in permissively infected cells. Two polyadenylated RNAs, of 4.9 and 2.3 kilobases, were the major species coded for by this region of the genome. These two RNAs, as well as a much less abundant RNA of 6.5 kilobases, were specifically altered in two different nononcogenic deletion mutants of H. saimiri. The 4.9- and 2.3-kilobase RNAs were mapped by S1 nuclease and exonuclease VII digestion of DNA-RNA hybrids. The transcripts were found to be spliced, overlapping, and transcribed from right to left on the genetic map, with their 3' termini each ca. 150 base pairs from the left border between the unique and repetitive DNA regions. These RNAs were not detected at immediate early times after infection. The possible role of these RNAs in the origin of the malignant T-cell lymphoma caused by this virus is discussed.

摘要

最近研究表明,在新世界灵长类动物中,疱疹病毒萨氏病毒基因组中一个对病毒复制并非必需的区域,却是其致癌性所必需的。我们已经检测了在允许性感染细胞中源自该基因组区域的RNA。两种多聚腺苷酸化RNA,分别为4.9千碱基和2.3千碱基,是该基因组区域编码的主要种类。这两种RNA,以及一种丰度低得多的6.5千碱基RNA,在疱疹病毒萨氏病毒的两种不同的非致癌缺失突变体中发生了特异性改变。通过对DNA-RNA杂交体进行S1核酸酶和核酸外切酶VII消化,对4.9千碱基和2.3千碱基的RNA进行了定位。发现这些转录本是剪接的、重叠的,并且在遗传图谱上从右向左转录,它们的3'末端各自距离独特DNA区域和重复DNA区域之间的左边界约150个碱基对。在感染后的早期未检测到这些RNA。本文讨论了这些RNA在该病毒引起的恶性T细胞淋巴瘤起源中的可能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b426/254555/1dbcfeda70e8/jvirol00128-0238-a.jpg

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