Munro Carol A, Selvaggini Serena, de Bruijn Irene, Walker Louise, Lenardon Megan D, Gerssen Bertus, Milne Sarah, Brown Alistair J P, Gow Neil A R
School of Medical Sciences, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK.
Mol Microbiol. 2007 Mar;63(5):1399-413. doi: 10.1111/j.1365-2958.2007.05588.x.
Chitin is an essential component of the fungal cell wall and its synthesis is under tight spatial and temporal regulation. The fungal human pathogen Candida albicans has a four member chitin synthase gene family comprising of CHS1 (class II), CHS2 (class I), CHS3 (class IV) and CHS8 (class I). LacZ reporters were fused to each CHS promoter to examine the transcriptional regulation of chitin synthesis. Each CHS promoter had a unique regulatory profile and responded to the addition of cell wall damaging agents, to mutations in specific CHS genes and exogenous Ca2+. The regulation of both CHS gene expression and chitin synthesis was co-ordinated by the PKC, HOG MAP kinase and Ca2+/calcineurin signalling pathways. Activation of these pathways also resulted in increased chitin synthase activity in vitro and elevated cell wall chitin content. Combinations of treatments that activated multiple pathways resulted in synergistic increases in CHS expression and in cell wall chitin content. Therefore, at least three pathways co-ordinately regulate chitin synthesis and activation of chitin synthesis operates at both transcriptional and post-transcriptional levels.
几丁质是真菌细胞壁的重要组成部分,其合成受到严格的空间和时间调控。人类真菌病原体白色念珠菌有一个由四个成员组成的几丁质合酶基因家族,包括CHS1(II类)、CHS2(I类)、CHS3(IV类)和CHS8(I类)。将LacZ报告基因与每个CHS启动子融合,以研究几丁质合成的转录调控。每个CHS启动子都有独特的调控模式,并对细胞壁损伤剂的添加、特定CHS基因突变和外源Ca2+作出反应。CHS基因表达和几丁质合成的调控由PKC、HOG丝裂原活化蛋白激酶和Ca2+/钙调神经磷酸酶信号通路协调。这些信号通路的激活还导致体外几丁质合酶活性增加和细胞壁几丁质含量升高。激活多个信号通路的联合处理导致CHS表达和细胞壁几丁质含量协同增加。因此,至少有三条信号通路协同调节几丁质合成,几丁质合成的激活在转录和转录后水平均起作用。