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禽肿瘤病毒感染细胞中病毒RNA的大小和遗传内容。

Size and genetic content of viral RNAs in avian oncovirus-infected cells.

作者信息

Hayward W S

出版信息

J Virol. 1977 Oct;24(1):47-63. doi: 10.1128/JVI.24.1.47-63.1977.

Abstract

Viral complementary DNA (cDNA) sequences corresponding to the gag, pol, env, src, and c regions of the Rous sarcoma virus genome were selected by hybridizing viral cDNA to RNA from viruses that lack the env or src gene or to polyadenylic acid [poly(A)]-containing RNA fragments of different lengths and isolating either hybridized or unhybridized DNA. The specificities, genetic complexities, and map locations of the selected cDNA's were shown to be in good agreement with the size and map locations of the corresponding viral genes. Analyses of virus-specific RNA, using the specific cDNA's as molecular probes, demonstrated that oncovirus-infected cells contained genome-length (30-40S) RNA plus either one or two species of subgenome-length viral RNA. The size and genetic content of these RNAs varied, depending on the genetic makeup of the infecting virus, but in each case the smaller RNAs contained only sequences located near the 3' end of the viral genome. Three RNA species were detected in Schmidt-Ruppin Rous sarcoma virus-infected cells: 39S (genome-length) RNA; 28S RNA, with an apparent sequence of env-src-c-poly(A); and 21S RNA, with an apparent sequence of src-c-poly(A). Cells infected with the Bryan high-titer strain of Rous sarcoma virus, which lacks the env gene, contained genome-length (35S) RNA and 21S src-specific RNA, but not the 28S RNA species. Leukosis virus-infected cells contained two detectable RNA species: 35S (genome-length) RNA and 21S RNA, with apparent sequence env-c-poly(A). Since gag and pol sequences were detected only in genome-length RNAs, it seems likely that the full-length transcripts function as mRNA for these two genes. The 28S and 21S RNAs could be the active messengers for the env and src genes. Analyses of sequence homologies among nucleic acids of different avian oncoviruses demonstrated substantial similarities within most of the genetic regions of these viruses. However, the "common" region of Rous-associated virus-0, an endogenous virus, was found to differ significantly from that of the other viruses tested.

摘要

通过使病毒互补DNA(cDNA)与缺乏env或src基因的病毒的RNA或与不同长度的含聚腺苷酸[poly(A)]的RNA片段杂交,并分离杂交或未杂交的DNA,选择了与劳氏肉瘤病毒基因组的gag、pol、env、src和c区域相对应的病毒cDNA序列。所选cDNA的特异性、遗传复杂性和图谱位置与相应病毒基因的大小和图谱位置高度一致。使用特异性cDNA作为分子探针分析病毒特异性RNA,结果表明肿瘤病毒感染的细胞含有基因组长度(30 - 40S)的RNA以及一种或两种亚基因组长度的病毒RNA。这些RNA的大小和遗传内容各不相同,这取决于感染病毒的基因组成,但在每种情况下,较小的RNA仅包含位于病毒基因组3'端附近的序列。在施密特 - 鲁平劳氏肉瘤病毒感染的细胞中检测到三种RNA:39S(基因组长度)RNA;28S RNA,其明显序列为env - src - c - poly(A);以及21S RNA,其明显序列为src - c - poly(A)。感染缺乏env基因的劳氏肉瘤病毒布莱恩高滴度株的细胞含有基因组长度(35S)RNA和21S src特异性RNA,但不含28S RNA。白血病病毒感染的细胞含有两种可检测到的RNA:35S(基因组长度)RNA和21S RNA,其明显序列为env - c - poly(A)。由于仅在基因组长度的RNA中检测到gag和pol序列,全长转录本似乎可能作为这两个基因的mRNA发挥作用。28S和21S RNA可能是env和src基因的活性信使。对不同禽肿瘤病毒核酸序列同源性的分析表明,这些病毒的大多数遗传区域内存在大量相似性。然而,发现内源性病毒劳氏相关病毒 - 0的“共同”区域与所测试的其他病毒有显著差异。

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