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来自肖普纤维瘤和恶性兔纤维瘤病毒基因组区域的早期RNA的转录图谱分析。

Transcriptional mapping of early RNA from regions of the Shope fibroma and malignant rabbit fibroma virus genomes.

作者信息

Cabirac G F, Mulloy J J, Strayer D S, Sell S, Leibowitz J L

出版信息

Virology. 1986 Aug;153(1):53-69. doi: 10.1016/0042-6822(86)90007-3.

Abstract

Malignant rabbit fibroma virus (MV) is a recombinant poxvirus derived from Shope fibroma virus (SFV) and rabbit myxoma virus (D. S. Strayer, E. Skaletsky, G. F. Cabirac, P. A. Sharp, L. B. Corbeil, S. Sell, and J. L. Leibowitz, 1983a, J. Immunol. 130, 399-404; W. Block, C. Upton, and G. McFadden, 1984, Virology 140, 113-124). We report here the transcriptional mapping of early RNAs transcribed from the SFV sequences within MV and from the corresponding regions in SFV. Hybridization analysis and S1 nuclease mapping of RNA using viral DNA probes were used to define 5' and 3' ends of the various transcripts. The RNAs described here are transcribed in one direction in a densely arranged head to tail fashion similar to that described for some vaccinia virus early transcriptional units. At late times of infection the early SFV RNAs are not detected whereas the early MV RNAs are present in minor amounts. The early SFV and MV transcripts range in size from 3170 to 425 nucleotides (nt) long. All of the longer transcripts are produced as a result of read through transcription. Three MV transcripts contain fused SFV and rabbit myxoma virus sequences due to transcription through the recombination junction region in the MV genome. Two other MV transcripts are transcribed from a unique initiation site near another recombination junction region resulting in RNAs that are composed of SFV sequences having unique 5' ends.

摘要

恶性兔纤维瘤病毒(MV)是一种重组痘病毒,源自肖普纤维瘤病毒(SFV)和兔黏液瘤病毒(D. S. 斯特雷耶、E. 斯凯莱茨基、G. F. 卡比拉克、P. A. 夏普、L. B. 科比尔、S. 塞尔和J. L. 莱博维茨,1983a,《免疫学杂志》130,399 - 404;W. 布洛克、C. 厄普顿和G. 麦克法登,1984,《病毒学》140,113 - 124)。我们在此报告从MV内的SFV序列以及SFV相应区域转录的早期RNA的转录图谱。使用病毒DNA探针进行RNA的杂交分析和S1核酸酶图谱分析,以确定各种转录本的5'和3'末端。此处描述的RNA以密集排列的头对头方式单向转录,类似于一些痘苗病毒早期转录单位的情况。在感染后期未检测到早期SFV RNA,而早期MV RNA少量存在。早期SFV和MV转录本的大小范围为3170至425个核苷酸(nt)长。所有较长的转录本都是通读转录的结果。由于通过MV基因组中的重组连接区转录,三个MV转录本包含融合的SFV和兔黏液瘤病毒序列。另外两个MV转录本从另一个重组连接区附近的独特起始位点转录,产生由具有独特5'末端的SFV序列组成的RNA。

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