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起始 tRNA 在 pre-mRNA 剪接调控中的潜在作用。

A potential role for initiator-tRNA in pre-mRNA splicing regulation.

机构信息

Department of Organic Chemistry, The Weizmann Institute of Science, Rehovot, Israel.

出版信息

Proc Natl Acad Sci U S A. 2010 Jun 22;107(25):11319-24. doi: 10.1073/pnas.0911561107. Epub 2010 Jun 7.

Abstract

The translation initiator-tRNA plays a crucial role in the initiation of protein synthesis in both prokaryotic and eukaryotic cells, by employing specific base pairing between its anticodon triplet CAU and the general initiation codon AUG in the mRNA. Here we show that the initiator-tRNA may also act, in a manner that is independent of its role in protein translation, as a pre-mRNA splicing regulator. Specifically, we show that alternative splicing events that are induced by mutations in the translation initiation AUG codon can be suppressed by expressing initiator-tRNA constructs carrying anticodon mutations that compensate for the AUG mutations. These mutated initiator-tRNAs appeared to be uncharged with an amino acid. Our results imply that recognition of the initiation AUG sequence by the anticodon triplet of initiator-tRNA in its unloaded state plays a role in quality control of splicing in the cell nucleus by a yet unresolved mechanism. Identifying the initiator-tRNA as a transacting splicing regulator suggests a novel involvement of this molecule in splicing regulation and provides a critical step toward deciphering this intriguing mechanism.

摘要

起始 tRNA 在原核和真核细胞的蛋白质合成起始中发挥着关键作用,通过其反密码子三核苷酸 CAU 与 mRNA 中通用起始密码子 AUG 之间的特异性碱基配对。在这里,我们表明起始 tRNA 可能以一种与其在蛋白质翻译中的作用无关的方式,作为前体 mRNA 剪接调节剂发挥作用。具体而言,我们表明,由翻译起始 AUG 密码子突变诱导的可变剪接事件可以通过表达带有反密码子突变的起始 tRNA 构建体来抑制,这些反密码子突变补偿了 AUG 突变。这些突变的起始 tRNA 似乎没有携带氨基酸。我们的结果表明,在未加载状态下,起始 tRNA 的反密码子三核苷酸对起始 AUG 序列的识别通过尚未阐明的机制在细胞核中剪接的质量控制中发挥作用。将起始 tRNA 鉴定为反式剪接调节因子表明该分子在剪接调节中的新参与,并为解析这一有趣机制提供了关键步骤。

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