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腺病毒核心在体外的转录

Transcription of adenovirus cores in vitro.

作者信息

Vayda M E, Leong K, Flint S J

出版信息

Virology. 1984 Nov;139(1):152-63. doi: 10.1016/0042-6822(84)90336-2.

Abstract

Transcription in whole HeLa cell extracts of the nucleoprotein core complexes released from adenovirus type 2 or type 5 virions has been examined. The average length of transcripts from deproteinized DNA templates increased steadily during a 90-min reaction in vitro, exhibiting an elongation rate of approximately 70 nucleotides per minute. On the other hand, transcripts made from viral core templates were restricted to a length of less than 2000 nucleotides. Accordingly, efficient transcription of cores (50 nucleotides elongated/min) ceased after 10-20 min of incubation in whole-cell extracts. Deproteinized viral DNA and viral nucleoprotein complexes appeared to support the initiation of a similar number of transcripts per template molecule, but the rate of initiation was faster when cores were provided as templates. Deproteinized viral DNA supported the synthesis of VA-RNA and of transcripts that hybridized to the region of the viral genome containing the 5' portion of the major late transcriptional. Viral cores also directed the synthesis of RNA products which hybridized to fragments of the viral genome containing E1A, E1B, and E4 regions. The results of nuclease protection experiments indicated that the presence of core proteins did not preclude accurate initiation of transcription from the E4 region.

摘要

对从2型或5型腺病毒病毒粒子中释放的核蛋白核心复合物在完整的HeLa细胞提取物中的转录情况进行了检测。在体外90分钟的反应过程中,来自脱蛋白DNA模板的转录本平均长度稳步增加,显示出每分钟约70个核苷酸的延伸速率。另一方面,由病毒核心模板产生的转录本长度限制在2000个核苷酸以下。因此,在全细胞提取物中孵育10 - 20分钟后,核心的有效转录(每分钟延伸50个核苷酸)就停止了。脱蛋白的病毒DNA和病毒核蛋白复合物似乎支持每个模板分子起始相似数量的转录本,但以核心作为模板时起始速率更快。脱蛋白的病毒DNA支持VA - RNA以及与包含主要晚期转录5'部分的病毒基因组区域杂交的转录本的合成。病毒核心还指导合成与包含E1A、E1B和E4区域的病毒基因组片段杂交的RNA产物。核酸酶保护实验结果表明,核心蛋白的存在并不妨碍从E4区域准确起始转录。

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