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首页> 外文期刊>The Journal of biological chemistry >Mne1 Is a Novel Component of the Mitochondrial Splicing Apparatus Responsible for Processing of a COX1 Group I Intron in Yeast
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Mne1 Is a Novel Component of the Mitochondrial Splicing Apparatus Responsible for Processing of a COX1 Group I Intron in Yeast

机译:MNE1是对酵母中Intron的COX1组的加工处理的线粒体剪接装置的新组分

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Saccharomyces cerevisiae cells lacking Mne1 are deficient in intron splicing in the gene encoding the Cox1 subunit of cytochrome oxidase but contain wild-type levels of the bc1 complex. Thus, Mne1 has no role in splicing of COB introns or expression of the COB gene. Northern experiments suggest that splicing of the COX1 aI5β intron is dependent on Mne1 in addition to the previously known Mrs1, Mss116, Pet54, and Suv3 factors. Processing of the aI5β intron is similarly impaired in mne1Δ and mrs1Δ cells and overexpression of Mrs1 partially restores the respiratory function of mne1Δ cells. Mrs1 is known to function in the initial transesterification reaction of splicing. Mne1 is a mitochondrial matrix protein loosely associated with the inner membrane and is found in a high mass ribonucleoprotein complex specifically associated with the COX1 mRNA even within an intronless strain. Mne1 does not appear to have a secondary function in COX1 processing or translation, because disruption of MNE1 in cells containing intronless mtDNA does not lead to a respiratory growth defect. Thus, the primary defect in mne1Δ cells is splicing of the aI5β intron in COX1.
机译:缺乏mne1的酿酒酵母细胞在编码细胞色素氧化酶的COX1亚基的基因中缺乏MNE1的细胞缺乏,但含有BC1络合物的野生型水平。因此,MNE1在剪接COB内含子或COB基因的表达中没有作用。北方实验表明,除了先前已知的MRS1,MS116,PET54和SUV3因子外,COX1AI5β内含子的剪接依赖于MNE1。 AI5β内含子的处理在MNE1δ和MRS1δ细胞中类似地损害MRS1Δ细胞和MRS1的过表达部分恢复MNE1Δ细胞的呼吸功能。已知MRS1在剪接的初始酯交换反应中起作用。 Mne1是与内膜松散地松散地相关的线粒体基质蛋白,并且在甚至在无元株内与COX1 mRNA有特异性相关的高质量核糖核糖蛋白复合物。 MNE1似乎在COX1处理或翻译中没有次要功能,因为含有内部MTDNA的细胞中的MNE1的破坏不会导致呼吸生长缺陷。因此,MNE1δ细胞的主要缺陷是COX1中AI5β内含子的剪接。

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