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裂殖酵母粟酒裂殖酵母的线粒体基因组。2. 通过种间杂交在ade7-50h-菌株中定位基因以及将基因组克隆为小片段。

The mitochondrial genome of the fission yeast Schizosaccharomyces pombe. 2. Localization of genes by interspecific hybridization in strain ade7-50h- and cloning of the genome in small fragments.

作者信息

Lang B F, Wolf K

出版信息

Mol Gen Genet. 1984;196(3):465-72. doi: 10.1007/BF00436194.

Abstract

A series of 18 small overlapping restriction fragments has been cloned, covering the complete mitochondrial genome of Schizosaccharomyces pombe. By hybridizing mitochondrial gene probes from Saccharomyces cerevisiae and Neurospora crassa with restriction fragments of Schizosaccharomyces pombe mitochondrial DNA, the following homologous genes were localized on the mitochondrial genome of S. pombe: cob, cox1, cox2 and cox3, ATPase subunit 6 and 9 genes, the large rRNA gene and both types of open reading frames occurring in mitochondrial introns of various ascomycetes. The region of the genome, hybridizing with cob exon probes is separated by an intervening sequence of about 2500 bp, which is homologous with the first two introns of the cox1 gene in Saccharomyces cerevisiae (class II introns according to Michel et al. 1982). Similarly, in the cox1 homologous region, which covers about 4000 bp, two regions were detected hybridizing with class I intron probes, suggesting the existence of two cox1 introns in Schizosaccharomyces pombe. Hybridization with several specific exon probes with a determined order has revealed that cob, cox1, cox3 and the large rRNA gene are all transcribed from the same DNA strand. The low intensities of hybridization signals suggest a large evolutionary distance between Schizosaccharomyces pombe and Saccharomyces cerevisiae or Neurospora crassa mitochondrial genes. Considering the length of the mitochondrial DNA of Schizosaccharomyces pombe (about 19.4 kbp) and the expected length of the localized genes and intron sequences there is enough space left for encoding the expected set of tRNAs and the small rRNA gene. The existence of leader-, trailer-, ori- and spacer sequences or further unassigned reading frames is then restricted to a total length of about 3000 bp only.

摘要

已克隆出一系列18个小的重叠限制性片段,覆盖了粟酒裂殖酵母的完整线粒体基因组。通过将来自酿酒酵母和粗糙脉孢菌的线粒体基因探针与粟酒裂殖酵母线粒体DNA的限制性片段杂交,以下同源基因被定位在粟酒裂殖酵母的线粒体基因组上:细胞色素b(cob)、细胞色素c氧化酶亚基1(cox1)、细胞色素c氧化酶亚基2(cox2)和细胞色素c氧化酶亚基3(cox3)、ATP合酶亚基6和9基因、大核糖体RNA基因以及各种子囊菌线粒体内含子中出现的两种类型的开放阅读框。与cob外显子探针杂交的基因组区域被一个约2500 bp的间隔序列隔开,该间隔序列与酿酒酵母中cox1基因的前两个内含子同源(根据Michel等人1982年的分类为II类内含子)。同样地,在覆盖约4000 bp的cox1同源区域中,检测到两个与I类内含子探针杂交的区域,这表明粟酒裂殖酵母中存在两个cox1内含子。用几个具有确定顺序的特定外显子探针进行杂交表明,cob、cox1、cox3和大核糖体RNA基因均从同一DNA链转录。杂交信号的低强度表明粟酒裂殖酵母与酿酒酵母或粗糙脉孢菌的线粒体基因之间存在较大的进化距离。考虑到粟酒裂殖酵母线粒体DNA的长度(约19.4 kbp)以及定位基因和内含子序列的预期长度,仍有足够的空间来编码预期的tRNA集和小核糖体RNA基因。那么前导序列、尾随序列、ori序列和间隔序列或其他未分配的阅读框的存在总共仅限制在约3000 bp的长度内。

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