Saiz J E, Santos M A, Vázquez de Aldana C R, Revuelta J L
Departamento de Microbiología y Genética, Universidad de Salamanca, Spain.
Yeast. 1999 Jan 30;15(2):155-64. doi: 10.1002/(SICI)1097-0061(19990130)15:2<155::AID-YEA342>3.0.CO;2-U.
In this report we describe the construction and basic phenotypic analysis of deletion mutants in six open reading frames (ORFs) of unknown function from the yeast Saccharomyces cerevisiae. Using the dominant kanMX marker and polymerase chain reaction (PCR) methods, deletion cassettes were constructed for five ORFs (YNL099c, YNL100w, YNL101w, YNL106c and YNL242w) located on chromosome XIV and one ORF (YOR109w) located on chromosome XV. The recovery of viable haploid deletant strains among the meiotic products of heterozygous deletants for each ORF demonstrated that none of the analysed ORFs was essential. With the exception of YNL242w, no alterations in growth characteristics or mating and sporulation efficiencies associated with deletion of the ORFs were observed. Homozygous diploid ynl242w delta cells obtained in three different genetic backgrounds were unable to sporulate, indicating that the product of this ORF is required for sporulation. Complementation of the sporulation defect by the cognate gene clone confirmed this observation. YNL106c and YOR109w are very similar and show strong sequence homology with a mammalian phosphatidylinositol-phosphate 5-phosphatase, synaptojanin, known to be involved in synaptic vesicle cycling. Strains bearing single and double deletions of YNL106c and YOR109w were seen to display abnormal vacuolar morphologies of varying degrees. Complementation tests indicated that YNL106c and YOR109w are redundant genes.
在本报告中,我们描述了酿酒酵母中6个功能未知的开放阅读框(ORF)缺失突变体的构建及基本表型分析。利用显性kanMX标记和聚合酶链反应(PCR)方法,构建了位于第XIV号染色体上的5个ORF(YNL099c、YNL100w、YNL101w、YNL106c和YNL242w)以及位于第XV号染色体上的1个ORF(YOR109w)的缺失盒。每个ORF的杂合缺失体减数分裂产物中可存活单倍体缺失菌株的回收表明,所分析的ORF均非必需。除YNL242w外,未观察到与ORF缺失相关的生长特性、交配和孢子形成效率的改变。在三种不同遗传背景下获得的纯合二倍体ynl242wΔ细胞无法形成孢子,表明该ORF的产物是孢子形成所必需的。同源基因克隆对孢子形成缺陷的互补证实了这一观察结果。YNL106c和YOR109w非常相似,与已知参与突触小泡循环的哺乳动物磷脂酰肌醇磷酸5-磷酸酶突触素具有很强的序列同源性。携带YNL106c和YOR109w单缺失和双缺失的菌株表现出不同程度的异常液泡形态。互补试验表明YNL106c和YOR109w是冗余基因。