Zeiner Gusti M, Hitchcock Robert A, Sturm Nancy R, Campbell David A
Department of Microbiology, Immunology, and Molecular Genetics, University of California at Los Angeles, 609 Charles E. Young Dr. East, Los Angeles, CA 90095-1489, USA.
Mol Cell Biol. 2004 Dec;24(23):10390-6. doi: 10.1128/MCB.24.23.10390-10396.2004.
In all trypanosomatids, trans splicing of the spliced leader (SL) RNA is a required step in the maturation of all nucleus-derived mRNAs. The SL RNA is transcribed with an oligo-U 3' extension that is removed prior to trans splicing. Here we report the identification and characterization of a nonexosomal, 3'-->5' exonuclease required for SL RNA 3'-end formation in Trypanosoma brucei. We named this enzyme SNIP (for snRNA incomplete 3' processing). The central 158-amino-acid domain of SNIP is related to the exonuclease III (ExoIII) domain of the 3'-->5' proofreading epsilon subunit of Escherichia coli DNA polymerase III holoenzyme. SNIP had a preference for oligo(U) 3' extensions in vitro. RNA interference-mediated knockdown of SNIP resulted in a growth defect and correlated with the accumulation of one- to two- nucleotide 3' extensions of SL RNA, U2 and U4 snRNAs, a five-nucleotide extension of 5S rRNA, and the destabilization of U3 snoRNA and U2 snRNA. SNIP-green fluorescent protein localized to the nucleoplasm, and substrate SL RNA derived from SNIP knockdown cells showed wild-type cap 4 modification, indicating that SNIP acts on SL RNA after cytosolic trafficking. Since the primary SL RNA transcript was not the accumulating species in SNIP knockdown cells, SL RNA 3'-end formation is a multistep process in which SNIP provides the ultimate 3'-end polishing. We speculate that SNIP is part of an organized nucleoplasmic machinery responsible for processing of SL RNA.
在所有锥虫中,剪接前导(SL)RNA的反式剪接是所有细胞核来源mRNA成熟过程中的一个必要步骤。SL RNA转录时带有一个寡聚U 3'末端延伸,该延伸在反式剪接之前被去除。在此,我们报告了在布氏锥虫中SL RNA 3'末端形成所需的一种非外切体3'→5'核酸外切酶的鉴定和特征。我们将这种酶命名为SNIP(用于snRNA不完全3'加工)。SNIP的中央158个氨基酸结构域与大肠杆菌DNA聚合酶III全酶3'→5'校对ε亚基的核酸外切酶III(ExoIII)结构域相关。SNIP在体外对寡聚(U)3'末端延伸具有偏好性。RNA干扰介导的SNIP敲低导致生长缺陷,并与SL RNA、U2和U4 snRNA的一到两个核苷酸3'末端延伸、5S rRNA的五个核苷酸延伸的积累以及U3 snoRNA和U2 snRNA的不稳定相关。SNIP-绿色荧光蛋白定位于核质,并且来源于SNIP敲低细胞的底物SL RNA显示出野生型帽4修饰,表明SNIP在胞质运输后作用于SL RNA。由于初级SL RNA转录本不是SNIP敲低细胞中积累的物种,SL RNA 3'末端形成是一个多步骤过程,其中SNIP提供最终的3'末端修饰。我们推测SNIP是负责SL RNA加工的有组织核质机制的一部分。