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大肠杆菌信使核糖核酸降解的特异性核酸内切酶切割位点

Specific endonucleolytic cleavage sites for decay of Escherichia coli mRNA.

作者信息

Cannistraro V J, Subbarao M N, Kennell D

出版信息

J Mol Biol. 1986 Nov 20;192(2):257-74. doi: 10.1016/0022-2836(86)90363-3.

Abstract

The polycistronic lac mRNA of Escherichia coli contains three messages. The rate of degradation of the second (lacY) message was observed to be equal to that of the third (lacA), and each decayed twice as fast as did the first (lacZ). Specific 5'- and 3'-ended lacY mRNA molecules could be recovered from cells; most likely, they are generated from endonucleolytic cleavages that are a part of the degradative process. They were observed by S1 nuclease mapping, and the exact 5'- and 3'-end oligonucleotides of many of them were identified by direct sequencing. Almost all of the molecules started with a 5' adenosine that would be preceded by a pyrimidine. The specificity was further restricted by neighboring nucleotides, and analysis of the data suggested that 5'-U-U decreases-A-U- is especially vulnerable. Also, computer analyses predicted the most stable secondary structures of selected segments of the mRNA and suggested that cleavages may only occur in regions of single strandedness. A model of mRNA degradation is proposed based on these observations and earlier ones. There is no unique target on a message for the initial inactivating attack: any region free of ribosomes is vulnerable, but for statistical reasons the initial attack of most molecules is near the ribosome-loading site. With no further ribosome loading, the newly unprotected 5' ends are "chopped off" at one of the next preferred target sites almost as fast as the last ribosomes moves down the mRNA.

摘要

大肠杆菌的多顺反子乳糖操纵子mRNA包含三条信息。观察到第二条(lacY)信息的降解速率与第三条(lacA)相等,且每条的降解速度都是第一条(lacZ)的两倍。可以从细胞中回收特定5'端和3'端的lacY mRNA分子;很可能,它们是由作为降解过程一部分的内切核酸酶切割产生的。通过S1核酸酶图谱观察到了它们,并通过直接测序鉴定了其中许多分子的确切5'端和3'端寡核苷酸。几乎所有分子都以一个5'腺苷开头,其前面会有一个嘧啶。特异性还受到相邻核苷酸的进一步限制,对数据的分析表明5'-U-U-decreases-A-U-尤其脆弱。此外,计算机分析预测了mRNA选定片段的最稳定二级结构,并表明切割可能仅发生在单链区域。基于这些观察结果和早期的观察结果,提出了一个mRNA降解模型。对于初始的失活攻击,信息上没有唯一的靶点:任何没有核糖体的区域都是脆弱的,但出于统计原因,大多数分子的初始攻击都在核糖体加载位点附近。由于没有进一步的核糖体加载,新暴露的5'端几乎会在最后一个核糖体沿着mRNA移动的同时,在下一个优先靶点之一被“切掉”。

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