Conde Raúl, Pablo Guadalupe, Cueva Rosario, Larriba Germán
Departamento de Microbiología, Facultad de Ciencias, Universidad de Extremadura, 06071 Badajoz, Spain.
Yeast. 2003 Oct 30;20(14):1189-211. doi: 10.1002/yea.1032.
We have carried out a screen of 622 deletion strains generated during the EUROFAN B0 project to identify non-essential genes related to the mannosylphosphate content of the cell wall. By examining the affinity of the deletants for the cationic dye alcian blue and the ion exchanger QAE-Sephadex, we have selected 50 strains. On the basis on their reactivity (blue colour intensity) in the alcian blue assay, mutants with a lower phosphate content than wild-type cells were then arranged in groups defined by previously characterized mutants, as follows: group I (mnn6), group II (between mnn6 and mnn9) and group III (mnn9). Similarly, strains that behaved like mnn1 (i.e. a blue colour deeper than wild-type) were included in group VI. To confirm the association between the phenotype and a specific mutation, strains were complemented with clones or subjected to tetrad analysis. Selected strains were further tested for extracellular invertase and exoglucanase. Within groups I, II and III, we found some genes known to be involved in oligosaccharide biosynthesis (ALG9, ALG12, HOC1), secretion (BRE5, COD4/COG5, VPS53), transcription (YOL072w/THP1, ELP2, STB1, SNF11), cell polarity (SEP7, RDG1), mitochondrial function (YFH1), cell metabolism, as well as orphan genes. Within group VI, we found genes involved in environmentally regulated transduction pathways (PAL2 and RIM20) as well as others with miscellaneous or unknown functions. We conclude that mannosylphosphorylation is severely impaired in some deletants deficient in specific glycosylation/secretion processes, but many other different pathways may also modulate the amount of mannosylphosphate in the cell wall.
我们对EUROFAN B0项目期间产生的622个缺失菌株进行了筛选,以鉴定与细胞壁甘露糖磷酸含量相关的非必需基因。通过检测缺失突变体对阳离子染料阿尔辛蓝和离子交换剂QAE-葡聚糖凝胶的亲和力,我们挑选出了50个菌株。然后,根据它们在阿尔辛蓝检测中的反应性(蓝色强度),将磷酸含量低于野生型细胞的突变体按照先前已鉴定的突变体定义的组别进行分类,如下:第一组(mnn6)、第二组(介于mnn6和mnn9之间)和第三组(mnn9)。同样,表现与mnn1相似(即蓝色比野生型更深)的菌株被归入第六组。为了证实表型与特定突变之间的关联,对菌株进行了克隆互补或四分体分析。对挑选出的菌株进一步检测其胞外转化酶和外切葡聚糖酶。在第一组、第二组和第三组中,我们发现了一些已知参与寡糖生物合成(ALG9、ALG12、HOC1)、分泌(BRE5、COD4/COG5、VPS53)、转录(YOL072w/THP1、ELP2、STB1、SNF11)、细胞极性(SEP7、RDG1)、线粒体功能(YFH1)、细胞代谢的基因,以及一些孤儿基因。在第六组中,我们发现了参与环境调节信号转导途径的基因(PAL2和RIM20)以及其他功能多样或未知的基因。我们得出结论,在一些特定糖基化/分泌过程缺陷的缺失突变体中,甘露糖磷酸化受到严重损害,但许多其他不同途径也可能调节细胞壁中甘露糖磷酸的含量。