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Evidence for the Identity of Shared 5′-Terminal Sequences Between Genome RNA and Subgenomic mRNAs of B77 Avian Sarcoma Virus

机译:B77禽肉瘤病毒基因组RNA和亚基因组mRNA之间共享5-末端序列同一性的证据

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摘要

The polyribosomal fraction from chicken embryo fibroblasts infected with B77 avian sarcoma virus contained 38S, 28S, and 21S virus-specific RNAs in which sequences identical to the 5′-terminal 101 bases of the 38S genome RNA were present. The only polyadenylic acid-containing RNA species with 5′ sequences which was detectable in purified virions had a sedimentation coefficient of 38S. This evidence is consistent with the hypothesis that a leader sequence derived from the 5′ terminus of the RNA is spliced to the bodies of the 28S and 21S mRNA's, both of which have been shown previously to be derived from the 3′ terminal half of the 38S RNA. The entire 101-base 5′ terminal sequence of the genome RNA appeared to be present in the majority of the subgenomic intracellular virus-specific mRNA's, as established by several different methods. First, the extent of hybridization of DNA complementary to the 5′-terminal 101 bases of the genome to polyadenylic acid-containing subgenomic RNA was similar to the extent of its hybridization to 38S RNA from infected cells and from purified virions. Second, the fraction of the total cellular polyadenylic acid-containing RNA with 5′ sequences was similar to the fraction of RNA containing sequences identical to the extreme 3′ terminus of the genome RNA when calculated by the rate of hybridization of the appropriate complementary DNA probes. This suggests that most intracellular virus-specific RNA molecules contain sequences identical to those present in the 5′-terminal 101 bases of the genome. Third, the size of most of the radioactively labeled DNA complementary to the 5′-terminal 101 bases of the genome remained unchanged after the probe was annealed to either intracellular 38S RNA or to various size classes of subgenomic RNA and the hybrids were digested with S1 nuclease and denatured with alkali. However, after this procedure some DNA fragments of lower molecular weight were present. This was not the case when the DNA complementary to the 5′-terminal 101 bases of the genome was annealed to 38S genome RNA. These results suggest that, although the majority of the intracellular RNA contains the entire 101-base 5′-terminal leader sequence, a small population of virus-specific RNAs exist that contain either a shortened 5′ leader sequence or additional splicing in the terminal 101 bases.
机译:感染了B77禽肉瘤病毒的鸡胚成纤维细胞的多核糖体级分包含38S,28S和21S病毒特异性RNA,其中存在与38S基因组RNA的5'-末端101个碱基相同的序列。在纯化的病毒体中可检测到的唯一具有5'序列的含聚腺苷酸的RNA种类的沉降系数为38S。该证据与以下假设相一致:从RNA 5'端衍生的前导序列被剪接到28S和21S mRNA的主体上,这两个序列先前都已证明是从RNA的3'末端一半衍生而来。 38S RNA。如通过几种不同的方法所建立的,基因组RNA的整个101个碱基的5'末端序列似乎存在于大多数亚基因组细胞内病毒特异性mRNA中。首先,与基因组的5'-末端101个碱基互补的DNA与含聚腺苷酸的亚基因组RNA的杂交程度类似于其与感染细胞和纯化病毒体与38S RNA杂交的程度。第二,当通过合适的互补DNA探针的杂交速率计算时,具有5'序列的总细胞含聚腺苷酸的RNA的分数与包含与基因组RNA的极端3'末端相同的序列的RNA的分数相似。 。这表明大多数细胞内病毒特异性RNA分子包含的序列与基因组5'-末端101个碱基中存在的序列相同。第三,将探针退火至细胞内38S RNA或不同大小类别的亚基因组RNA并用S1消化杂交后,与基因组5'-末端101个碱基互补的大多数放射性标记DNA的大小保持不变。核酸酶并用碱变性。然而,在该程序之后,存在一些较低分子量的DNA片段。当与基因组5'-末端101个碱基互补的DNA与38S基因组RNA退火时,情况并非如此。这些结果表明,尽管大多数细胞内RNA包含完整的101个碱基的5'-末端前导序列,但仍存在少量病毒特异性RNA,它们在101末端包含缩短的5'前导序列或其他剪接基地。

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