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莫洛尼氏鼠肉瘤病毒(M-MSV)与莫洛尼氏鼠白血病病毒(M-MLV)RNA序列关系的异源双链研究

A heteroduplex study of the sequence relationships between the RNAs of M-MSV and M-MLV.

作者信息

Hu S, Davidson N

出版信息

Cell. 1977 Mar;10(3):469-77. doi: 10.1016/0092-8674(77)90034-4.

DOI:10.1016/0092-8674(77)90034-4
PMID:844103
Abstract

The regions of sequence homology between the RNA genomes of a murine sarcoma virus (clone 124 Moloney-MSV) and its parental helper virus (clone 3 Moloney-murine leukemia virus (M-MLV)) have been mapped. Long complementary DNA transcripts of the M-MLV RNA were hybridized to M-MSV RNA, and the structures of the hybrids were observed in the electron microscope. Beginning at the 5' end, the two RNAs are homologous for a region of length 2.25 kb (kilobases). In the next region, of length approximately 4.2 kb on the MLV genome, there are several homology segments between MLV and MSV, but there are also several short sequences present on MLV and deleted in MSV. There is then a major substitution loop; with a sequence (beta L) of length 2.9 kb present on MLV and missing on MSV, and a sequence (beta S) of length 1.5 kb present on MSV and missing on MLV. At the 3' end, there is a homology sequence of length 0.8 kb. On the basis of these results, other data on genes expressed in M-MSV-transformed cells, and by analogy with the avian gene map, we suggest that the gag genes (internal structural proteins) lie in the 2.25 kb region of homology near the 5' ends of M-MSV and M-MLV RNAs, and that the beta S segment contains a sarcoma (src) gene. Some of the heteroduplexes and some of the MLV cDNA/MLV RNA homoduplexes are circular, thus showing that cDNA transcription is initiated at an internal position in the RNA, proceeds to the 5' end, and them "jumps" to the 3' end.

摘要

已绘制出鼠肉瘤病毒(克隆124莫洛尼 - 鼠肉瘤病毒(MSV))及其亲本辅助病毒(克隆3莫洛尼 - 鼠白血病病毒(M - MLV))的RNA基因组之间的序列同源区域。将M - MLV RNA的长互补DNA转录本与M - MSV RNA杂交,并在电子显微镜下观察杂交体的结构。从5'端开始,两种RNA在长度为2.25 kb(千碱基)的区域内同源。在MLV基因组上接下来长度约为4.2 kb的区域中,MLV和MSV之间有几个同源片段,但MLV上也有几个短序列在MSV中缺失。然后有一个主要的替代环;有一个长度为2.9 kb的序列(βL)存在于MLV上而在MSV中缺失,还有一个长度为1.5 kb的序列(βS)存在于MSV上而在MLV中缺失。在3'端,有一个长度为0.8 kb的同源序列。基于这些结果、关于M - MSV转化细胞中表达的基因的其他数据以及与禽基因图谱的类比,我们认为gag基因(内部结构蛋白)位于M - MSV和M - MLV RNA 5'端附近长度为2.25 kb的同源区域,并且βS片段包含一个肉瘤(src)基因。一些异源双链体和一些MLV cDNA/MLV RNA同源双链体是环状的,因此表明cDNA转录在RNA的内部位置起始,延伸至5'端,然后“跳跃”至3'端。

相似文献

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A heteroduplex study of the sequence relationships between the RNAs of M-MSV and M-MLV.莫洛尼氏鼠肉瘤病毒(M-MSV)与莫洛尼氏鼠白血病病毒(M-MLV)RNA序列关系的异源双链研究
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引用本文的文献

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J Virol. 1980 May;34(2):464-73. doi: 10.1128/JVI.34.2.464-473.1980.
2
Biogenesis of a transforming gene.一种转化基因的生物发生
Mol Biol Rep. 1981 May 22;7(1-3):163-5. doi: 10.1007/BF00778748.
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Analysis of the env gene of a molecularly cloned and biologically active Moloney mink cell focus-forming proviral DNA.
对分子克隆且具有生物活性的莫洛尼貂细胞病灶形成前病毒DNA的env基因进行分析。
J Virol. 1982 Oct;44(1):19-31. doi: 10.1128/JVI.44.1.19-31.1982.
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Isolation of a transformation-defective deletion mutant of Moloney murine sarcoma virus.莫洛尼氏鼠肉瘤病毒转化缺陷型缺失突变体的分离
J Virol. 1982 Feb;41(2):735-43. doi: 10.1128/JVI.41.2.735-743.1982.
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J Virol. 1982 May;42(2):538-46. doi: 10.1128/JVI.42.2.538-546.1982.
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