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聚腺苷酸(poly(A))限制元件对poly(A)长度调控的位置和序列要求

Position and sequence requirements for poly(A) length regulation by the poly(A) limiting element.

作者信息

Gupta J D, Gu H, Schoenberg D R

机构信息

Department of Molecular and Cellular Biochemistry, The Ohio State University, Columbus 43210, USA.

出版信息

RNA. 2001 Jul;7(7):1034-42. doi: 10.1017/s1355838201010329.

Abstract

The poly(A)-limiting element (PLE) is a cis-acting sequence that acts to limit poly(A) tail length on pre-mRNA to <20 nt. Functional PLEs are present in a number of genes, underscoring the generality of this control mechanism. The current study sought to define further the position requirements for poly(A) length regulation and the core sequence that comprises a PLE. Increasing the spacing between the PLE and the upstream 3' splice site or between the PLE and the downstream AAUAAA had no effect on poly(A) length control. However, moving the PLE from the terminal exon to either an upstream exon or intron eliminated poly(A) length control. Poly(A) length control was further evaluated using a battery of constructs in which the PLE was maintained in the terminal exon, but where upstream introns were either deleted, modified, or replaced with a polypyrimidine tract. Poly(A) length control was retained in all cases, indicating that the key feature is the presence of the PLE in the terminal exon. A battery of mutations demonstrated the importance of the 5' pyrimidine-rich portion of the element. Finally, UV crosslinking experiments identified an approximately 62-kDa protein in Hela nuclear extract that binds to a wild-type 23-nt PLE RNA oligonucleotides but not to a mutated nonfunctional form of the element.

摘要

聚腺苷酸限制元件(PLE)是一种顺式作用序列,其作用是将前体mRNA上的聚腺苷酸尾巴长度限制在<20个核苷酸。功能性PLE存在于许多基因中,这突出了这种调控机制的普遍性。当前的研究旨在进一步确定聚腺苷酸长度调控的位置要求以及构成PLE的核心序列。增加PLE与上游3'剪接位点之间或PLE与下游AAUAAA之间的间距对聚腺苷酸长度控制没有影响。然而,将PLE从末端外显子移至上游外显子或内含子会消除聚腺苷酸长度控制。使用一系列构建体进一步评估聚腺苷酸长度控制,其中PLE保留在末端外显子中,但上游内含子被删除、修饰或被多嘧啶序列取代。在所有情况下聚腺苷酸长度控制均得以保留,表明关键特征是末端外显子中存在PLE。一系列突变证明了该元件富含5'嘧啶部分的重要性。最后,紫外线交联实验在HeLa细胞核提取物中鉴定出一种约62 kDa的蛋白质,它能与野生型23个核苷酸的PLE RNA寡核苷酸结合,但不能与该元件的突变无功能形式结合。

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本文引用的文献

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Proc Natl Acad Sci U S A. 1999 Aug 3;96(16):8943-8. doi: 10.1073/pnas.96.16.8943.
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