首页> 外文期刊>Yeast >Screening for new yeast mutants affected in mannosylphosphorylation of cell wall mannoproteins [Review]
【24h】

Screening for new yeast mutants affected in mannosylphosphorylation of cell wall mannoproteins [Review]

机译:筛选受细胞壁甘露糖蛋白甘露糖基磷酸化影响的新酵母突变体[综述]

获取原文
获取原文并翻译 | 示例
           

摘要

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 1, 11 and 111, 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.
机译:我们已经对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基磷酸含量有关的非必需基因。通过检查缺失剂对阳离子染料阿尔辛蓝和离子交换剂QAE-Sephadex的亲和力,我们选择了50个菌株。根据其在阿尔辛蓝测定法中的反应性(蓝色强度),将磷酸盐含量低于野生型细胞的突变体排列在先前表征的突变体定义的组中,如下所示:I组(mnn6),II组(介于mnn6和mnn9之间)和群组III(mnn9)。类似地,在第VI组中包括表现为mnn1(即比野生型更深的蓝色)的菌株。为了证实表型和特定突变之间的关联,用克隆对菌株进行互补或进行四联体分析。进一步测试了所选菌株的细胞外转化酶和葡聚糖酶。在第1、11和111组中,我们发现了一些已知参与寡糖生物合成的基因(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),细胞代谢以及孤儿基因。在第六组中,我们发现了与环境调控的转导途径有关的基因(PAL2和RIM20)以及其他具有其他功能或未知功能的基因。我们得出的结论是,在某些缺乏特定糖基化/分泌过程的缺失中,甘露糖基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基磷酸的含量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号