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人腺病毒2感染细胞中DNA链特异性早期信使RNA种类的分离

Isolation of DNA Strand-specific early messenger RNA species in cells infected by human adenovirus 2.

作者信息

Büttner W, Veres-Molnár Z, Green M

出版信息

Proc Natl Acad Sci U S A. 1974 Aug;71(8):2951-5. doi: 10.1073/pnas.71.8.2951.

Abstract

Hybridization to the separated light (L) and heavy (H) strands of adenovirus 2 DNA in 50% formamide at 37 degrees was used to isolate undegraded virus-specific RNA molecules from the polyribosomes of cycloheximide-treated human KB cells early after infection with adenovirus 2. About 20% of polyribosomal RNA labeled with [(3)H]uridine from 4 to 7 hr after infection was virus-specific. Twice as much labeled RNA was homologous to the L strand as to the H strand. Polyacrylamide gel electrophoresis of RNA selected with unfractionated adenovirus DNA resolved a major component of virus-specific RNA in the 19-20 S region of the gel and smaller amounts of viral RNA in two heterogeneous fractions migrating at 15-18 S and 21-26 S. Selection with individual DNA strands showed that the 19-20 S main size class of early mRNA consists of two homogeneous RNA species with slightly different mobilities, the transcripts from the L and H strand having molecular weights of 7.4 x 10(5) and 7.7 x 10(5), respectively. The 15-18 S RNA hybridized with the L strand and the 21-26 S RNA with the H strand.

摘要

在37℃下于50%甲酰胺中,将腺病毒2 DNA的轻链(L)和重链(H)进行杂交,用于从感染腺病毒2后早期经环己酰亚胺处理的人KB细胞的多核糖体中分离未降解的病毒特异性RNA分子。感染后4至7小时用[³H]尿苷标记的多核糖体RNA中约20%是病毒特异性的。与L链同源的标记RNA量是与H链同源的两倍。用未分级的腺病毒DNA选择的RNA进行聚丙烯酰胺凝胶电泳,在凝胶的19 - 20 S区域分辨出病毒特异性RNA的主要成分,在15 - 18 S和21 - 26 S迁移的两个异质组分中有少量病毒RNA。用单链DNA选择表明,早期mRNA的19 - 20 S主要大小类由两种迁移率略有不同的均一RNA物种组成,L链和H链的转录本分子量分别为7.4×10⁵和7.7×10⁵。15 - 18 S RNA与L链杂交,21 - 26 S RNA与H链杂交。

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