Center for RNA Biology, The Ohio State University, Columbus, OH, USA.
Department of Biological Chemistry and Pharmacology, The Ohio State University College of Medicine, Columbus, OH, USA.
FEBS Lett. 2019 Apr;593(7):670-679. doi: 10.1002/1873-3468.13349. Epub 2019 Mar 9.
Until cytoplasmic recapping was discovered, decapping was thought to irreversibly destine an mRNA to degradation. Contradicting this idea, we readily observe mRNAs targeted by cytoplasmic capping in uncapped, yet stable forms. 5' rapid amplification of cDNA ends (RACE) shows that nearly all uncapped ends correspond to capped analysis of gene expression tags and that the recapping of ZNF207 mRNA may be restricted to a single splice isoform. Here, a modified RACE approach detected uncapped 5' RNA ends mapping to 46 mRNAs in cells expressing a dominant negative cytoplasmic capping enzyme and in normal cells. Eleven of 46 cloned mRNAs also contained splice isoform-limiting sequences. Collectively, these data reinforce earlier work and suggest that alternative splicing may play a role in targeting transcripts for - and/or determining the position of - cytoplasmic capping.
直到细胞质重新帽化被发现,去帽化被认为不可逆转地使 mRNA 降解。与这个观点相反,我们很容易观察到细胞质帽化靶向的 mRNAs 以未帽化但稳定的形式存在。5' 快速扩增 cDNA 末端 (RACE) 显示,几乎所有未帽化的末端都对应于有帽分析的基因表达标签,并且 ZNF207 mRNA 的重新帽化可能仅限于单一剪接异构体。在这里,一种改良的 RACE 方法检测到表达显性细胞质帽化酶的细胞和正常细胞中未帽化的 5' RNA 末端映射到 46 个 mRNAs。46 个克隆的 mRNAs 中有 11 个也含有剪接异构体限制序列。总的来说,这些数据强化了早期的工作,并表明选择性剪接可能在靶向转录物和/或确定细胞质帽化的位置方面发挥作用。