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一个在RNA转运方面存在缺陷的剪接连接缺失不会使核RNA聚腺苷酸化。

A splice junction deletion deficient in the transport of RNA does not polyadenylate nuclear RNA.

作者信息

Villarreal L P, White R T

出版信息

Mol Cell Biol. 1983 Aug;3(8):1381-8. doi: 10.1128/mcb.3.8.1381-1388.1983.

Abstract

A late region deletion mutant of simian virus 40 (dl5) was previously shown to be deficient in the transport of nuclear RNA. This is a splice junction deletion that has lost the 3' end of an RNA leader, an intervening sequence, and the 5' end of the splice acceptor site on the body of the mRNA. In this report, we analyzed the steady-state structure of the untransported nuclear RNA. The 5' ends of this RNA are heterogeneous but contain a prominent 5' end at the normal position (nucleotide 325) in addition to several other prominent 5' ends not seen in wild-type RNA. The 3' end of this RNA does not occur at the usual position (nucleotide 2674) of polyadenylation; instead, this RNA is non-polyadenylated, with the 3' end occurring either downstream or upstream of the normal position.

摘要

猿猴病毒40(dl5)的一个晚期区域缺失突变体先前已被证明在核RNA转运方面存在缺陷。这是一个剪接连接缺失,它丢失了RNA前导序列的3'端、一个间隔序列以及mRNA主体上剪接受体位点的5'端。在本报告中,我们分析了未转运的核RNA的稳态结构。该RNA的5'端是异质性的,但除了野生型RNA中未出现的其他几个突出的5'端外,在正常位置(核苷酸325)还含有一个突出的5'端。该RNA的3'端并非出现在通常的多聚腺苷酸化位置(核苷酸2674);相反,该RNA是非多聚腺苷酸化的,其3'端出现在正常位置的下游或上游。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dd2/369984/ccb99c02a841/molcellb00108-0057-a.jpg

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