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猴病毒40早期信使核糖核酸。I. 来自转化细胞和裂解感染细胞的信使核糖核酸中3'和5'末端以及两个主要剪接位点的基因组定位。

Simian virus 40 early mRNA's. I. Genomic localization of 3' and 5' termini and two major splices in mRNA from transformed and lytically infected cells.

作者信息

Reddy V B, Ghosh P K, Lebowitz P, Piatak M, Weissman S M

出版信息

J Virol. 1979 Apr;30(1):279-96. doi: 10.1128/JVI.30.1.279-296.1979.

Abstract

We have studied the structure of polyadenylated virus-specific cytoplasmic mRNA's in mouse and human cells transformed by simian virus 40 and in monkey cells infected with simian virus 40 in the presence of cytosine arabinoside by means of reverse transcriptase-catalyzed complementary DNA synthesis and complementary DNA sequencing. Abundant mRNA species containing splices from residues 4490 to 4557 (0.533 to 0.546 map units [m.u.]) and 4490 to 4837 (0.533 to 0.600 m.u.) were identified in both transformed and infected cells. Two principal reverse transcriptase stops were observed at the 5' termini of these mRNA's, both occurring with approximately equal frequency. The most distal of these stops was localized at residues 5152 to 5154 (0.660 m.u.), and the second was at residues 5147 to 5148 (0.659 m.u.). Several additional minor stops, between approximately 0.62 and 0.65 m.u., were also found on complementary DNA copied from transformed cell mRNA; in contrast, only one additional stop was present on complementary DNA copied from early lytic mRNA. These data suggest the presence of a prinicipal 5' terminus of early lytic and transformed cell mRNA's at residues 5152 to 5154 and raise the possibility of additional 5' termini at one or more locations in the 0.62 to 0.659 m.u. region of these mRNA's. Transformed cell mRNA was also found to contain a single 3' terminus at positions 2504 and 2505 (0.153 m.u.); termini lying beyond this site were not detected.

摘要

我们通过逆转录酶催化的互补DNA合成和互补DNA测序,研究了在猿猴病毒40转化的小鼠和人类细胞以及在阿糖胞苷存在下感染猿猴病毒40的猴细胞中,多聚腺苷酸化的病毒特异性细胞质mRNA的结构。在转化细胞和感染细胞中均鉴定出了丰富的mRNA种类,其剪接片段来自4490至4557位残基(0.533至0.546个图距单位[m.u.])以及4490至4837位残基(0.533至0.600 m.u.)。在这些mRNA的5'末端观察到两个主要的逆转录酶终止位点,二者出现的频率大致相等。其中最远端的终止位点位于5152至5154位残基(0.660 m.u.),第二个位于5147至5148位残基(0.659 m.u.)。在从转化细胞mRNA复制的互补DNA上还发现了几个额外的次要终止位点,大约在0.62至0.65 m.u.之间;相比之下,从早期裂解mRNA复制的互补DNA上仅存在一个额外的终止位点。这些数据表明早期裂解和转化细胞mRNA的主要5'末端位于5152至5154位残基处,并增加了在这些mRNA的0.62至0.659 m.u.区域中一个或多个位置存在额外5'末端的可能性。还发现转化细胞mRNA在2504和2505位(0.153 m.u.)含有单个3'末端;未检测到位于该位点之外的末端。

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