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首页> 外文期刊>Yeast >Disruption of six novel ORFs on the left arm of chromosome XII reveals onegene essential for vegetative growth of Saccharomyces cerevisiae
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Disruption of six novel ORFs on the left arm of chromosome XII reveals onegene essential for vegetative growth of Saccharomyces cerevisiae

机译:XII染色体左臂上六个新ORF的破坏揭示了酿酒酵母营养生长必不可少的一个基因

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Deletion via PCR-mediated gene replacement, together with basic functional and bioinformatic analyses, have been performed on six novel open reading-frames (ORFs) on the left arm of chromosome XII of Saccharomyces cerevisiae (YLL033w, YLL032c, YLL031c, YLL030c, YLL029w and YLL028w). ORF deletion was realized using either a short-flanking homology (SFH) or a long-flanking homology (LFH) replacement cassette in the diploid strain FY1679. Sporulation and tetrad analysis showed that YLL031c is the only essential gene of the six. Microscopic examination of the non-growing spores carrying a disrupted copy of the essential gene showed that most of them were blocked after one or two cell divisions with heterogeneous bud size. The standard EUROFAN growth tests failed to reveal any obvious phenotype resulting from the deletion of each the five non-essential ORFs. Bioinformatic analysis revealed that YLL029w is probably an aminopeptidase for mitochondrial or nuclear protein processing and YLL028w may be involved in drug resistance in S. cerevisiae. Replacement cassettes, comprising the promoter and terminator regions of each of the six ORFs, were cloned into pUG7 and demonstrated to efficiently mediate gene replacement in an alternative diploid strain, W303. All the cognate gene clones were constructed, using either PCR products amplified from genomic DNA, or gap-repair. All clones and strains generated have been deposited in the EUROFAN genetic stock centre (EUROSCARF, Frankfurt). Copyright (C) 1999 John Wiley & Sons, Ltd.
机译:通过PCR介导的基因置换的删除,以及基本的功能和生物信息学分析,已在酿酒酵母XII染色体左臂(YLL033w,YLL032c,YLL031c,YLL030c,YLL029w和YLL029w和YLL028w)。使用二倍体菌株FY1679中的短侧同源(SFH)或长侧同源(LFH)替换盒可实现ORF缺失。孢子形成和四联体分析表明YLL031c是这六个中的唯一必需基因。显微镜检查未生长的带有必需基因拷贝的孢子,结果显示,大多数芽孢在一到两个细胞分裂后,芽大小不一,被阻断。标准的EUROFAN生长测试未能揭示出由于删除了五个非必需ORF而导致的任何明显表型。生物信息学分析表明,YLL029w可能是线粒体或核蛋白加工的氨基肽酶,YLL028w可能与酿酒酵母的耐药性有关。将包含六个ORF中每一个的启动子和终止子区域的替换盒克隆到pUG7中,并证明可在另一种二倍体菌株W303中有效介导基因替换。使用从基因组DNA扩增的PCR产物或缺口修复构建所有同源基因克隆。产生的所有克隆和菌株均已保存在EUROFAN遗传储备中心(EUROSCARF,法兰克福)中。版权所有(C)1999 John Wiley&Sons,Ltd.

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