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腺病毒2型(Ad2)信使核糖核酸(mRNA)加工步骤:多聚腺苷酸(poly(A))加尾的核序列得以保留,且多聚腺苷酸化先于剪接发生。

Steps in the processing of Ad2 mRNA: poly(A)+ nuclear sequences are conserved and poly(A) addition precedes splicing.

作者信息

Nevins J R, Darnell J E

出版信息

Cell. 1978 Dec;15(4):1477-93. doi: 10.1016/0092-8674(78)90071-5.

Abstract

The conservation of nuclear Ad2 sequences during nucleocytoplasmic transport has been estimated from the accumulation of 3H-uridine in nuclear and cytoplasmic Ad2-specific RNA from the major late transcription unit. From 10-28% is conserved of the total Ad2 nuclear RNA synthesized from each of five regions of the genome that specify groups of 3' co-terminal mRNAs. The sum of the conservation of all the regions was equivalent to 100%, signifying the conservation of at least a part of each transcript or all of about one fifth to one sixth of the transcripts. The conservation of poly(A)+ Ad2 nuclear RNA is about 4 times greater than of total Ad2 nuclear RNA, approaching 100% conservation of poly(A)+ nuclear sequences. Since each mRNA contains three "spliced" sequences that are probably encoded only once per transcript, these data on conservation of the Ad2 sequences suggest that each transcriptional event from the 16-99 transcription unit gives rise to one of a possible 13-14 mRNA molecules with destruction of the remainder of the transcribed RNA. The portion which is conserved resides next to the region to which which poly(A) is added. Three models for the choice of poly(A) sites were considered: termination at the poly(A) site, cleavage shortly after synthesis of one of the sites before transcription was complete, and cleavage after completion of transcription. The first model was ruled out by the demonstration of equimolar synthesis over the 16-99 region. The second model is strongly supported because 3H-uridine label appears equally rapidly in the time range 2-10 min in each of the five 3' poly(A) addition sites, whereas chain completion before cleavage would lead to a faster appearance of label in the most promoter-distal site. Furthermore, briefly labeled RNA molecules extending from 16 to each of several poly(A) addition sites were the first poly(A)- terminated 3H-uridine-labeled molecules detected, demonstrating that poly(A) addition precedes splicing. The choice of which mRNA emerges from each transcriptional event would appear to depend upon first choosing one of five 3' mRNA ends followed by a 5' splicing event.

摘要

通过测量3H-尿苷在核内和胞质中来自主要晚期转录单位的腺病毒2型(Ad2)特异性RNA中的积累情况,估算了核质转运过程中Ad2序列的保守性。从基因组五个区域中的每个区域合成的Ad2核RNA总量中,有10%-28%是保守的,这五个区域分别指定了3' 共末端mRNA的组。所有区域保守性的总和相当于100%,这意味着每个转录本的至少一部分是保守的,或者约五分之一到六分之一的转录本全部保守。聚腺苷酸化(poly(A)+)的Ad2核RNA的保守性比总Ad2核RNA大约高4倍,接近poly(A)+核序列100%的保守性。由于每个mRNA包含三个“剪接”序列,每个转录本可能只编码一次,这些关于Ad2序列保守性的数据表明,来自16-99转录单位的每个转录事件会产生13-14种可能的mRNA分子中的一种,同时转录的其余RNA会被降解。保守的部分位于添加poly(A)的区域旁边。考虑了三种选择poly(A)位点的模型:在poly(A)位点终止、在转录完成前合成其中一个位点后不久进行切割以及转录完成后进行切割。通过在16-99区域进行等摩尔合成的证明排除了第一个模型。第二个模型得到了有力支持,因为在2-10分钟的时间范围内,3H-尿苷标记在五个3' poly(A)添加位点中的每个位点出现的速度相同,而在切割前完成链延伸会导致在最远离启动子的位点更快出现标记。此外,从16延伸到几个poly(A)添加位点中的每个位点的短暂标记RNA分子是最早检测到的poly(A)终止的3H-尿苷标记分子,这表明poly(A)添加先于剪接。每个转录事件产生哪种mRNA的选择似乎首先取决于从五个3' mRNA末端中选择一个,然后是5' 剪接事件。

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