Suppr超能文献

RNA聚合酶II在体外的启动子近端暂停:短于20个核苷酸的转录本没有加帽。

Promoter-proximal pausing by RNA polymerase II in vitro: transcripts shorter than 20 nucleotides are not capped.

作者信息

Coppola J A, Field A S, Luse D S

出版信息

Proc Natl Acad Sci U S A. 1983 Mar;80(5):1251-5. doi: 10.1073/pnas.80.5.1251.

Abstract

We have synthesized RNA from cloned adenovirus 2 late promoter DNA in an in vitro transcription extract under UTP-limiting conditions. Under these circumstances, almost all of the alpha-amanitin-sensitive RNA produced is shorter than 20 nucleotides; most of these short transcripts are present in four species, 6, 7, 13, and 17 nucleotides. These short RNAs are initiated at the adenovirus 2 promoter, as judged by partial sequence analysis and by the abolition of their synthesis upon cleavage of the template DNA at sites which also abolish the production of full-length transcripts. All of the short transcripts can be chased, with excess UTP, into 197-base run-off transcripts; thus, these RNAs are precursors of full-length transcripts and not synthetic "dead ends." Significantly, none of these short RNAs is capped or 2'-O-methylated. However, 79-base run-off transcripts synthesized from this promoter with nonlimiting NTP levels are fully capped.

摘要

我们在体外转录提取物中,于UTP受限条件下,从克隆的腺病毒2晚期启动子DNA合成了RNA。在这些情况下,几乎所有产生的α-鹅膏蕈碱敏感RNA都短于20个核苷酸;这些短转录本大多存在于四种类型中,分别为6、7、13和17个核苷酸。通过部分序列分析以及在那些也会消除全长转录本产生的位点切割模板DNA后其合成的消除来判断,这些短RNA在腺病毒2启动子处起始。所有短转录本在加入过量UTP后,都能被追踪转化为197个碱基的连续转录本;因此,这些RNA是全长转录本的前体,而非合成的“死端”。值得注意的是,这些短RNA均未进行加帽或2'-O-甲基化修饰。然而,在非限制性NTP水平下从该启动子合成的79个碱基的连续转录本是完全加帽的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb12/393573/b6b1c5488edf/pnas00631-0101-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验