首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >The inducible N-acetylglucosamine catabolic pathway gene cluster in Candida albicans: Discrete N-acetylglucosamine-inducible factors interact at the promoter of NAG1
【2h】

The inducible N-acetylglucosamine catabolic pathway gene cluster in Candida albicans: Discrete N-acetylglucosamine-inducible factors interact at the promoter of NAG1

机译:诱导型N-乙酰氨基葡萄糖分解代谢 白色念珠菌的途径基因簇:离散 N-乙酰氨基葡萄糖诱导因子在 NAG1的启动子

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The catabolic pathway of N-acetylglucosamine (GlcNAc) in Candida albicans is an important facet of its pathogenicity. One of the pathway genes, encoding glucosamine-6-phosphate deaminase (NAG1) is transcriptionally regulated by GlcNAc. Sequence analysis of a 4-kb genomic clone containing NAG1 indicates that this gene is part of a cluster containing two other genes of the GlcNAc catabolic pathway, i.e., DAC1, GlcNAc-6-phosphate deacetylase, and HXK1, hexokinase. All three genes are temporally and coordinately induced by GlcNAc suggesting a common regulatory mechanism for these genes. The NAG1 promoter is up-regulated when induced by GlcNAc in C. albicans but not in Saccharomyces cerevisiae. In vivo analysis of the deletion constructs delineated the minimal promoter to −130 bp and mapped two regions at −200 and −400 bp upstream of +1 (ATG) responsible for GlcNAc induction. Gel mobility-shift assays and “footprinting” (DNase protection method) analyses revealed two regions, 5′-GGAGCAAAAAAATGT 3′ (−164 to −150, box A) and 5′-ACGGTGAGTTG 3′ (−291 to −281, box B), that are recognized and bound by at least two inducible activator proteins directing the regulation of gene expression.
机译:白色念珠菌中N-乙酰氨基葡萄糖(GlcNAc)的分解代谢途径是其致病性的重要方面。 GlcNAc转录调控的一种途径基因,编码6-氨基葡萄糖氨基葡萄糖(NAG1)。含有NAG1的4-kb基因组克隆的序列分析表明,该基因是含有GlcNAc分解代谢途径的其他两个基因(即DAC1,GlcNAc-6-磷酸脱乙酰酶和HXK1己糖激酶)的簇的一部分。这三个基因在时间和坐标上均由GlcNAc诱导,提示了这些基因的共同调控机制。当由GlcNAc诱导在白色念珠菌中而不是在酿酒酵母中时,NAG1启动子被上调。缺失构建体的体内分析将最小启动子描绘为-130 bp,并将两个区域(负责GlcNAc诱导)定位在+1(ATG)的-200和-400 bp处。凝胶迁移率变动分析和“足迹”(DNA酶保护方法)分析揭示了两个 5'-GGAGCAAAAAAATGT 3'区域(-164至-150,方框A)和 5'-ACGGTGAGTTG 3'(-291至-281,方框B), 结合至少两种诱导蛋白 基因表达的调控。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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