首页> 外文期刊>Bioscience, Biotechnology, and Biochemistry >Upregulation of Genes Involved in Gluconeogenesis and the Glyoxylate Cycle Suppressed the Drug Sensitivity of an N-Glycan-Deficient Saccharomyces cerevisiae Mutant
【24h】

Upregulation of Genes Involved in Gluconeogenesis and the Glyoxylate Cycle Suppressed the Drug Sensitivity of an N-Glycan-Deficient Saccharomyces cerevisiae Mutant

机译:涉及糖原异生和乙醛酸循环的基因的上调抑制了N-聚糖缺陷型酿酒酵母突变体的药物敏感性。

获取原文
获取原文并翻译 | 示例
       

摘要

Saccharomyces cerevisiae strain TIY20, which produces a mammalian high-mannose type N-glycan, exhibits a severe growth defect due to disruption of yeast-specific outer chain mannosyltransferases. We have isolated a more fit strain, YAB103, from TIY20 by the use of a novel mutagenesis technique based on the disparity theory of evolution. To determine why YAB103 lacked the growth defect and the hygromycin B sensitivity of its parent, TIY20, gene expression profiles of YAB103 and TIY20 were analyzed using DNA microarrays. Expression of genes that encode enzymes in the gluconeogenesis pathway and glyoxylate cycle, which produce glucose 6-phophate and its derivatives, was up-regulated in YAB103. Up-regulation of these genes suppressed the drug sensitivity of the TIY20 strain. Furthermore, we found that YAB103 had a thicker cell-wall due to an increase in glucan content. To our knowledge, this is first report linking N-glycosyla-tion to gluconeogenesis and the glyoxylate cycle.
机译:产生哺乳动物高甘露糖型N-聚糖的酿酒酵母菌株TIY20由于酵母特异性外链甘露糖基转移酶的破坏而显示出严重的生长缺陷。通过使用基于进化差异理论的新型诱变技术,我们从TIY20中分离了更合适的菌株YAB103。为了确定为什么YAB103缺乏其母体TIY20的生长缺陷和潮霉素B敏感性,使用DNA微阵列分析了YAB103和TIY20的基因表达谱。在YAB103中上调了糖异生途径和乙醛酸循环中编码酶的基因的表达,这些酶产生6-磷酸葡萄糖及其衍生物。这些基因的上调抑制了TIY20菌株的药物敏感性。此外,我们发现,由于葡聚糖含量的增加,YAB103的细胞壁更厚。据我们所知,这是第一个将N-糖基化与糖异生和乙醛酸循环联系起来的报道。

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