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鉴定参与胰岛素样生长因子-II(IGF-II)信使核糖核酸(mRNA)位点特异性切割的RNA序列和结构。

Identification of RNA sequences and structures involved in site-specific cleavage of IGF-II mRNAs.

作者信息

van Dijk E L, Sussenbach J S, Holthuizen P E

机构信息

Laboratory for Physiological Chemistry, Utrecht University, The Netherlands.

出版信息

RNA. 1998 Dec;4(12):1623-35. doi: 10.1017/s1355838298981316.

Abstract

Insulin-like growth factor-II (IGF-II) mRNAs are subject to site-specific endonucleolytic cleavage in the 3' untranslated region (UTR), rendering an unstable 5' cleavage product containing the coding region and a very stable 3' cleavage product of 1.8 kb consisting of the 3'-UTR sequence and the poly(A) tail. Previously, it was established that two widely separated elements in the 3'-UTR (elements I and II), that can form a duplex structure, are necessary and sufficient for cleavage. To further investigate the sequence and secondary structure requirements for cleavage, we have introduced a number of mutations around the cleavage site and assayed their effects on cleavage. Several recognition determinants involved in the endonucleolytic cleavage of IGF-II mRNAs were identified. Mutational analysis around the cleavage site revealed that cleavage is sequence specific and that the cleavage site must be in a single-stranded conformation to allow efficient cleavage. In addition, we have identified an accessory protein that specifically interacts with a stem-loop structure located 133 to 73 nt upstream of the cleavage site.

摘要

胰岛素样生长因子-II(IGF-II)信使核糖核酸(mRNAs)在3'非翻译区(UTR)会发生位点特异性内切核酸酶切割,产生一个不稳定的包含编码区的5'切割产物和一个由3'-UTR序列及多聚腺苷酸(poly(A))尾组成的1.8 kb非常稳定的3'切割产物。此前已确定,3'-UTR中两个相距甚远的元件(元件I和元件II),它们能形成双链结构,对于切割而言是必需且足够的。为了进一步研究切割的序列和二级结构要求,我们在切割位点周围引入了一些突变,并检测它们对切割的影响。确定了一些参与IGF-II mRNAs内切核酸酶切割的识别决定因素。切割位点周围的突变分析表明,切割具有序列特异性,且切割位点必须处于单链构象才能实现高效切割。此外,我们还鉴定出一种辅助蛋白,它能与位于切割位点上游133至73个核苷酸处的茎环结构特异性相互作用。

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