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一个21个碱基对的DNA片段指导猴病毒40晚期前导区内的转录衰减。

A 21-base pair DNA fragment directs transcription attenuation within the simian virus 40 late leader.

作者信息

Kessler M, Ben-Asher E, Resenkov O, Hatini V, Bengal E, Aloni Y

机构信息

Department of Molecular Genetics and Virology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

J Biol Chem. 1991 Jul 15;266(20):13019-27.

PMID:1649173
Abstract

Transcription through the late simian virus 40 (SV40) sequences have been examined in vivo and in vitro for identifying attenuation signals involved in regulating late RNA transcription. In addition to the previously identified and characterized attenuator 1 situated 93 nucleotides downstream from the major late transcription start site, a second attenuator, attenuator 2, situated 55 nucleotides downstream from it, has been identified. Attenuated transcripts mapping to this site have been observed in vivo as well as in several different in vitro transcription systems. The signal inducing transcription attenuation has been localized to a 21-base pair DNA fragment and has been found to function independently of the promoter directing transcription or its distance from the transcription start site. Furthermore, this attenuator, unlike that preceding it, does not include a region of dyad symmetry or A+T-rich sequences. Also, similar to the adenovirus 2 attenuator, but in contrast to SV40 attenuator 1, the block to elongation at the SV40 attenuator 2 appears to be modulated by the general transcription factors. It is concluded that in SV40 there are at least two types of attenuators: one that is dependent on RNA secondary structure and a second that is sequence specific and is modulated, at least in part, by the general transcription factors.

摘要

为了鉴定参与调节晚期RNA转录的衰减信号,已在体内和体外对猿猴病毒40(SV40)晚期序列的转录进行了研究。除了先前鉴定并表征的位于主要晚期转录起始位点下游93个核苷酸处的衰减子1外,还鉴定出了第二个衰减子,即衰减子2,它位于衰减子1下游55个核苷酸处。在体内以及几种不同的体外转录系统中都观察到了定位到该位点的衰减转录本。诱导转录衰减的信号已定位到一个21碱基对的DNA片段,并且已发现其功能独立于指导转录的启动子或其与转录起始位点的距离。此外,与之前的衰减子不同,这个衰减子不包括二元对称区域或富含A+T的序列。同样,与腺病毒2衰减子类似,但与SV40衰减子1不同,SV40衰减子2处的延伸阻滞似乎受一般转录因子调节。得出的结论是,在SV40中至少有两种类型的衰减子:一种依赖于RNA二级结构,另一种是序列特异性的,并且至少部分受一般转录因子调节。

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