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来自酿酒酵母和道格拉斯酵母的NAM2蛋白是线粒体亮氨酰-tRNA合成酶,并且参与mRNA剪接。

The NAM2 proteins from S. cerevisiae and S. douglasii are mitochondrial leucyl-tRNA synthetases, and are involved in mRNA splicing.

作者信息

Herbert C J, Labouesse M, Dujardin G, Slonimski P P

机构信息

Centre de Génétique Moléculaire du CNRS, Laboratoire propre associé à l'Université Pierre et Marie Curie, Gif-sur-Yvette, France.

出版信息

EMBO J. 1988 Feb;7(2):473-83. doi: 10.1002/j.1460-2075.1988.tb02835.x.

Abstract

We have cloned and sequenced the NAM2 gene of Saccharomyces douglasii, which is a homologue of the NAM2 gene of Saccharomyces cerevisiae. The wild-type S.douglasii gene possesses the suppressor functions of the mutant S. cerevisiae NAM2-1 allele, being able to cure a mitochondrial b14 maturase deficiency. By sequence comparisons and direct measurements we have demonstrated that the NAM2 genes encode mitochondrial leucyl tRNA synthetases (EC 6.1.1.4.). Using a derivative of the NAM2 gene, where the expression of the gene is under the control of the UAS GAL10, we have shown that the processing of the pre-mRNA from the two mosaic genes oxi3 and cob-box is impaired when transcription of the gene is repressed. These results lead us to conclude that the mitochondrial leucyl tRNA synthetase is involved in protein synthesis and mRNA splicing. Sequence comparisons show that the mitochondrial and Escherichia coli leucyl tRNA synthetases are highly homologous; however, significant features which may be important for the splicing functions of the mitochondrial enzymes are absent from the bacterial enzyme.

摘要

我们已经克隆并测序了道格拉斯酿酒酵母的NAM2基因,它是酿酒酵母NAM2基因的同源物。野生型道格拉斯酿酒酵母基因具有突变型酿酒酵母NAM2 - 1等位基因的抑制功能,能够治愈线粒体b14成熟酶缺陷。通过序列比较和直接测量,我们证明NAM2基因编码线粒体亮氨酰tRNA合成酶(EC 6.1.1.4.)。使用NAM2基因的一个衍生物,其中该基因的表达受UAS GAL10控制,我们已经表明,当该基因的转录被抑制时,来自两个嵌合基因oxi3和cob - box的前体mRNA的加工受到损害。这些结果使我们得出结论,线粒体亮氨酰tRNA合成酶参与蛋白质合成和mRNA剪接。序列比较表明,线粒体和大肠杆菌亮氨酰tRNA合成酶高度同源;然而,细菌酶缺乏可能对线粒体酶的剪接功能很重要的显著特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d07d/454344/95f3e5887375/emboj00139-0177-a.jpg

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