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一种来自感染2型腺病毒的细胞的新型病毒编码低分子量RNA。

A new species of virus-coded low molecular weight RNA from cells infected with adenovirus type 2.

作者信息

Söderlund H, Pettersson U, Vennström B, Philipson L, Mathews M B

出版信息

Cell. 1976 Apr;7(4):585-93. doi: 10.1016/0092-8674(76)90209-9.

Abstract

A virus-coded low molecular weight RNA (5.2S), which migrates slightly faster on polyacrylamide gels than the well characterized adenovirus-specific 5.5S RNA, has been isolated from cells infected with adenovirus type 2. Hybridization-competition experiments and RNA fingerprints indicate that the two virus-associated (VA) RNAs differ in their primary structures. The gene for 5.2S RNA is located to the right of the gene for 5.5S RNA, on the I strand of a DNA segment which extends between positions 30.3 and 32.2 on the map of adenovirus type 2 DNA. Both 5.5S and 5.2S RNA can be detected early after infection and also in the presence of cytosine-arabinoside or cycloheximide. After the onset of viral DNA replication, the synthesis of 5.2S RNA levels off, whereas 5.5S RNA is synthesized in increasing amounts. Both 5.2S and 5.5S RNAs are synthesized in isolated nuclei by an enzyme which resembles RNA polymerase III in its sensitivity to alpha-amanitin. In isolated nuclei, both RNA species are labeled with beta-32P-labeled GTP, which suggests that they are initiated at separate promotor sites.

摘要

从感染2型腺病毒的细胞中分离出一种病毒编码的低分子量RNA(5.2S),它在聚丙烯酰胺凝胶上的迁移速度比特征明确的腺病毒特异性5.5S RNA稍快。杂交竞争实验和RNA指纹图谱表明,这两种病毒相关(VA)RNA的一级结构不同。5.2S RNA基因位于5.5S RNA基因的右侧,在2型腺病毒DNA图谱上位置30.3和32.2之间延伸的DNA片段的I链上。5.5S和5.2S RNA在感染后早期以及在存在阿糖胞苷或环己酰亚胺的情况下都能被检测到。病毒DNA复制开始后,5.2S RNA的合成趋于平稳,而5.5S RNA的合成量不断增加。5.2S和5.5S RNA在分离的细胞核中由一种对α-鹅膏蕈碱敏感性类似于RNA聚合酶III的酶合成。在分离的细胞核中,这两种RNA都用β-32P标记的GTP进行标记,这表明它们在不同的启动子位点起始。

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