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Disruption of 12 ORFs located on chromosomes IV, VII and XIV of Saccharomyces cerevisiae reveals two essential genes

机译:位于酿酒酵母IV,VII和XIV染色体上的12个ORF的破坏揭示了两个必需基因

摘要

We describe the generation of null-mutants of 12 open reading frames (ORFs), discovered during the systematic sequencing of the Saccharomyces cerevisiae genome. These ORFs are located on chromosome IV (YDL183c), on chromosome VII (YGL139w, YGL140c, YGL141w, YGR280c and YGR284c) or on chromosome XIV (YNL006w, YNR004w, YNR007c, YNR008w, YNR009w and YNR013c). Disruptants were generated using the PCR-based short flanking homology (SFH) strategy in yeast strain FY1679. Tetrad analysis, following sporulation of the heterozygous disruptants, revealed that YGR280c and YNL006w are essential genes for vegetative yeast growth in rich medium. The lethality of the two genes was confirmed by gene complementation analysis. The protein encoded by YNL006w (LST8) is now known to be involved in transport of permeases from the Golgi to the plasma membrane. Basic phenotypic analyses were performed on haploid disruptants from both mating types of 10 non-essential genes. One disruptant (YNR004w) revealed a slow growth rate on glucose-minimal medium at 15 degrees C. For each of the individual ORFs, a disruption cassette and the corresponding cognate gene were cloned into appropriate plasmids.
机译:我们描述了酿酒酵母基因组的系统测序过程中发现的12个开放阅读框(ORF)的空突变体的生成。这些ORF位于IV染色体(YDL183c),VII染色体(YGL139w,YGL140c,YGL141w,YGR280c和YGR284c)或XIV染色体(YNL006w,YNR004w,YNR007c,YNR008w,YNR009w和YNR013c)。使用基于PCR的短侧翼同源性(SFH)策略在酵母FY1679中产生干扰物。在对杂合破坏子进行孢子形成后的Tetrad分析表明,YGR280c和YNL006w是营养酵母在丰富培养基中生长的必需基因。通过基因互补分析证实了这两个基因的致死性。现在已知由YNL006w(LST8)编码的蛋白质与渗透酶从高尔基体到质膜的运输有关。对来自10个非必需基因的两种交配类型的单倍体破坏基因进行了基本表型分析。一种破坏剂(YNR004w)显示在15摄氏度的葡萄糖最小培养基上生长缓慢。对于每个单独的ORF,将破坏盒和相应的同源基因克隆到适当的质粒中。

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