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对鼠白血病病毒21S RNA上5'前导序列的分析:利用长逆转录酶产物进行异源双链图谱分析。

Analysis of a 5' leader sequence on murine leukemia virus 21S RNA: heteroduplex mapping with long reverse transcriptase products.

作者信息

Rothenberg E, Donoghue D J, Baltimore D

出版信息

Cell. 1978 Mar;13(3):435-51. doi: 10.1016/0092-8674(78)90318-5.

Abstract

The majority of the mRNA that specifies retrovirus glycoproteins is known to be derived from the 3' half of the genome. To examine whether the glycoprotein mRNA of murine leukemia viruses (MuLVs) might consist of portions derived from both the 5' and 3' ends of the viral genome, we performed hybridization with a 5'-specific probe and heteroduplex analysis with long reverse transcribed DNA. A 5' probe was made by purifying a discrete 50 nucleotide-long reverse transcript attached to its tRNA primer. This probe was found to hybridize to RNA of the size of glycoprotein mRNA--21S, poly(A)-containing RNA--indicating that the mRNA could have a 5' leader sequence. The 5'-specific sequences were studied by electron microscopic examination of hybrids between 21S RNA and the two longest discrete cDNA species synthesized in the endogenous reverse transcriptase reaction. One of these species, 8.8 kb long, is only made in the absence of actinomycin D, but it does not contain any self-complementary sequences, and therefore appears to be a complete transcript of the viral genome. The shorter of the two species, 8.2 kb long, is synthesized whether or not actinomycin D is present; it must terminate 500--600 nucleotides internal to the 5' end of the template RNA. The structures observed in heteroduplexes of 21S RNA and these DNAs indicated the presence of a leader sequence approximately 500 nucleotides long at the 5' end of the 21S RNA. Sequences comprising this leader segment in the 21S RNA mapped at the 5' end of the genome RNA; the rest of the 21S RNA consisted of sequences from the 3' portion of the genome. Analysis of heteroduplexes with 8.2 kb DNA suggested that actinomycin D could block the reverse transcription of most of the sequence in the genome RNA that appears as a leader in the 21S RNA.

摘要

已知指定逆转录病毒糖蛋白的大多数mRNA来源于基因组的3' 半区。为了研究鼠白血病病毒(MuLVs)的糖蛋白mRNA是否可能由病毒基因组5' 和3' 端的部分组成,我们用5' 特异性探针进行杂交,并对长逆转录DNA进行异源双链分析。通过纯化附着于其tRNA引物的50个核苷酸长的离散逆转录产物制备了5' 探针。发现该探针与糖蛋白mRNA大小的RNA——含poly(A)的21S RNA杂交,表明该mRNA可能有一个5' 前导序列。通过电子显微镜检查21S RNA与内源性逆转录酶反应中合成的两个最长离散cDNA物种之间的杂交体,研究了5' 特异性序列。其中一个物种长8.8 kb,仅在没有放线菌素D的情况下产生,但它不包含任何自我互补序列,因此似乎是病毒基因组的完整转录本。两个物种中较短的一个长8.2 kb,无论是否存在放线菌素D都会合成;它必须在模板RNA 5' 端内部500 - 600个核苷酸处终止。在21S RNA与这些DNA的异源双链体中观察到结构表明,21S RNA的5'端存在一个约500个核苷酸长的前导序列。21S RNA中构成该前导片段的序列定位在基因组RNA的5'端;21S RNA的其余部分由基因组3'部分的序列组成。用8.2 kb DNA对异源双链体的分析表明,放线菌素D可以阻断基因组RNA中大部分在21S RNA中表现为前导序列的序列的逆转录。

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