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Beyond tRNA cleavage: novel essential function for yeast tRNA splicing endonuclease unrelated to tRNA processing

机译:超越tRNA裂解:与tRNA加工无关的酵母tRNA剪接核酸内切酶的新型基本功能

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摘要

Pre-tRNA splicing is an essential process in all eukaryotes. In yeast and vertebrates, the enzyme catalyzing intron removal from pre-tRNA is a heterotetrameric complex (splicing endonuclease [SEN] complex). Although the SEN complex is conserved, the subcellular location where pre-tRNA splicing occurs is not. In yeast, the SEN complex is located at the cytoplasmic surface of mitochondria, whereas in vertebrates, pre-tRNA splicing is nuclear. We engineered yeast to mimic the vertebrate cell biology and demonstrate that all three steps of pre-tRNA splicing, as well as tRNA nuclear export and aminoacylation, occur efficiently when the SEN complex is nuclear. However, nuclear pre-tRNA splicing fails to complement growth defects of cells with defective mitochondrial-located splicing, suggesting that the yeast SEN complex surprisingly serves a novel and essential function in the cytoplasm that is unrelated to tRNA splicing. The novel function requires all four SEN complex subunits and the catalytic core. A subset of pre-rRNAs accumulates when the SEN complex is restricted to the nucleus, indicating that the SEN complex moonlights in rRNA processing. Thus, findings suggest that selection for the subcellular distribution of the SEN complex may reside not in its canonical, but rather in a novel, activity.
机译:在所有真核生物中,pre-tRNA剪接是必不可少的过程。在酵母和脊椎动物中,催化从pre-tRNA去除内含子的酶是异四聚体复合物(剪接内切核酸酶[SEN]复合物)。尽管SEN复合体是保守的,但tRNA前剪接发生的亚细胞位置却不是。在酵母中,SEN复合体位于线粒体的细胞质表面,而在脊椎动物中,tRNA前的剪接是有核的。我们对酵母进行了工程改造,以模仿脊椎动物的细胞生物学,并证明了当SEN复合物为核时,tRNA剪接的所有三个步骤以及tRNA的核输出和氨基酰化作用均有效发生。然而,核pre-tRNA剪接不能通过线粒体定位的剪接来补充细胞的生长缺陷,这表明酵母SEN复合体出人意料地在与tRNA剪接无关的细胞质中发挥了新的必不可少的功能。新功能需要所有四个SEN复杂亚基和催化核心。当SEN复合物被限制在细胞核中时,前rRNA的一个子集会积累,这表明SEN复合物在rRNA加工过程中表现出月光。因此,发现表明对SEN复合物亚细胞分布的选择可能不在于其规范,而在于其新颖的活性。

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