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来自道格拉斯酿酒酵母的CBP2基因是酿酒酵母基因的功能同源物,对于在野生型(含内含子)线粒体基因组存在的情况下进行呼吸生长至关重要。

The CBP2 gene from Saccharomyces douglasii is a functional homologue of the Saccharomyces cerevisiae gene and is essential for respiratory growth in the presence of a wild-type (intron-containing) mitochondrial genome.

作者信息

Li G Y, Tian G L, Slonimski P P, Herbert C J

机构信息

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

出版信息

Mol Gen Genet. 1996 Feb 25;250(3):316-22. doi: 10.1007/BF02174389.

DOI:10.1007/BF02174389
PMID:8602146
Abstract

In Saccharomyces cerevisiae the only known role of the CBP2 gene is the excision of the fifth intron of the mitochondrial cyt b gene (bI5). We have cloned the CBP2 gene from Saccharomyces douglasii (a close relative of S. cerevisiae). A comparison of the S. douglasii and S. cerevisiae sequences shows that there are 14% nucleotide substitutions in the coding region, with transitions being three times more frequent than transversions. At the protein level sequence identity is 87%. We have demonstrated that the S. douglasii CBP2 gene is essential for respiratory growth in the presence of a wild-type S. douglasii mitochondrial genome, but not in the presence of an intronless S. cerevisiae mitochondrial genome. Also the S. douglasii and S. cerevisiae CBP2 genes are completely interchangeable, even though the intron bI5 is absent from the S. douglasii mitochondrial genome.

摘要

在酿酒酵母中,CBP2基因唯一已知的作用是切除线粒体细胞色素b基因(bI5)的第五个内含子。我们从道格拉斯酿酒酵母(酿酒酵母的近亲)中克隆了CBP2基因。对道格拉斯酿酒酵母和酿酒酵母序列的比较表明,编码区有14%的核苷酸替换,转换的频率是颠换的三倍。在蛋白质水平上,序列同一性为87%。我们已经证明,在存在野生型道格拉斯酿酒酵母线粒体基因组的情况下,道格拉斯酿酒酵母CBP2基因对于呼吸生长是必需的,但在无内含子的酿酒酵母线粒体基因组存在的情况下则不是。此外,道格拉斯酿酒酵母和酿酒酵母的CBP2基因是完全可互换的,尽管道格拉斯酿酒酵母线粒体基因组中不存在内含子bI5。

相似文献

1
The CBP2 gene from Saccharomyces douglasii is a functional homologue of the Saccharomyces cerevisiae gene and is essential for respiratory growth in the presence of a wild-type (intron-containing) mitochondrial genome.来自道格拉斯酿酒酵母的CBP2基因是酿酒酵母基因的功能同源物,对于在野生型(含内含子)线粒体基因组存在的情况下进行呼吸生长至关重要。
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引用本文的文献

1
The Cbp2 protein stimulates the splicing of the omega intron of yeast mitochondria.Cbp2蛋白刺激酵母线粒体ω内含子的剪接。
Nucleic Acids Res. 1997 Apr 15;25(8):1597-604. doi: 10.1093/nar/25.8.1597.

本文引用的文献

1
Sequence of the mitochondrial gene encoding subunit I of cytochrome oxidase in Saccharomyces douglasii.道格拉斯酿酒酵母细胞色素氧化酶亚基I线粒体基因序列
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Protein facilitation of group I intron splicing by assembly of the catalytic core and the 5' splice site domain.
蛋白质通过催化核心和5'剪接位点结构域的组装促进I组内含子剪接。
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7
Assembly of the mitochondrial membrane system. Characterization of a yeast nuclear gene involved in the processing of the cytochrome b pre-mRNA.线粒体膜系统的组装。一个参与细胞色素b前体mRNA加工的酵母核基因的特性分析。
J Biol Chem. 1983 Aug 10;258(15):9459-68.
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Transformation of intact yeast cells treated with alkali cations.经碱金属阳离子处理的完整酵母细胞的转化
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9
Genetic applications of yeast transformation with linear and gapped plasmids.使用线性和缺口质粒进行酵母转化的遗传学应用。
Methods Enzymol. 1983;101:228-45. doi: 10.1016/0076-6879(83)01017-4.
10
A mutation in yeast mitochondrial DNA results in a precise excision of the terminal intron of the cytochrome b gene.酵母线粒体DNA中的一个突变导致细胞色素b基因末端内含子的精确切除。
J Biol Chem. 1985 Mar 25;260(6):3235-8.