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腺病毒的体外转录

In vitro transcription of adenovirus.

作者信息

Fire A, Baker C C, Manley J L, Ziff E B, Sharp P A

出版信息

J Virol. 1981 Dec;40(3):703-19. doi: 10.1128/JVI.40.3.703-719.1981.

Abstract

A series of recombinants of adenovirus DNA fragments and pBR322 was used to test the transcriptional activity of the nine known adenovirus promoters in a cell-free extract. Specific initiation was seen at all five early promoters as well as at the major late promotor and at the intermediate promoter for polypeptide IX. The system failed to recognize the two other adenovirus promoters, which were prominent in vivo only at intermediate and late stages in infection. Microheterogeneity of 5' termini at several adenovirus promoters, previously shown in vivo, was reproduced in the in vitro reaction and indeed appeared to result from heterogeneous initiation rather than 5' processing. To test for the presence of soluble factors involved in regulation of nRNA synthesis, the activity of extracts prepared from early and late stages of infection was compared on an assortment of viral promoter sites. Although mock and early extracts showed identical transcription patterns, extracts prepared from late stages gave 5- to 10-fold relative enhancement of the late and polypeptide IX promoters as compared with early promoters.

摘要

一系列腺病毒DNA片段与pBR322的重组体用于检测无细胞提取物中九个已知腺病毒启动子的转录活性。在所有五个早期启动子、主要晚期启动子以及多肽IX的中间启动子处均可见特异性起始。该系统未能识别另外两个腺病毒启动子,这两个启动子仅在感染的中期和晚期在体内才显著。先前在体内显示的几个腺病毒启动子5'末端的微异质性在体外反应中重现,并且确实似乎是由异质起始而非5'加工导致的。为了检测参与nRNA合成调控的可溶性因子的存在,比较了从感染早期和晚期制备的提取物在各种病毒启动子位点上的活性。尽管模拟提取物和早期提取物显示出相同的转录模式,但与早期启动子相比,从晚期制备的提取物使晚期启动子和多肽IX启动子的相对活性提高了5至10倍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5590/256682/8f73993058b8/jvirol00165-0092-a.jpg

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