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The Candida albicans histidine kinase Chk1p: Signaling and cell wall mannan

机译:白色念珠菌组氨酸激酶Chk1p:信号传导和细胞壁甘露聚糖

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Several published functions associated with the CHK1 histidine kinase of Candida albicans resemble those of the MAPK Cek1p and its cognate receptor Sho1p (SSU81). To explore this further, we have compared mutants lacking the proteins mentioned above and have constructed a double sho1/chk1 Delta null mutant to determine relationships among these proteins. We observed that the sensitivity to Congo red (CR), calcofluor white (CW), as well as clumping of cells, was slightly increased in the double mutant compared to the single chk1 Delta or sho1 Delta mutants. However, Cek1p phosphorylation via Sho1p, which occurs during log phase growth in the presence or absence of CR in Wt cells, does not require Chk1p. These data suggest that Chk1p and Sho1p are components of parallel but independent signal pathways. In addition, bulk mannan of strains was analyzed by GLC/MS and GPC MALLS and NMR. Compared to Wt and a CHK1 gene-reconstituted strain (CHK23) that contained high, intermediate and low Mw mannan species, we found that the mannan of strains CHK21 (chk1 Delta null), the cek1 Delta null, and the double mutant consisted only of low Mw mannan. The sho1 Delta null mutant only demonstrated a reduced intermediate type of mannan. Alcian blue binding was lower in cek1 Delta, chk1 Delta, and the double sho1/chk1 Delta null mutant lacking high and intermediate Mw mannan than in the sho1 Delta null which had a partial loss of intermediate Mw mannan only. We conclude that the Chk1p HK is part of a functionally similar but parallel pathway to the Sho1p-Cek1p pathway that confers resistance to the cell wall inhibitors CR and CW. However, a functional relationship in mannan biosynthesis of Chk1p and Cek1p exists that only partially requires Sho1p.
机译:与白色念珠菌的CHK1组氨酸激酶相关的几种已公开功能与MAPK Cek1p及其同源受体Sho1p(SSU81)相似。为了进一步探讨这一点,我们比较了缺少上述蛋白质的突变体,并构建了一个双sho1 / chk1 Delta无效突变体来确定这些蛋白质之间的关系。我们观察到,与单个chk1 Delta或sho1 Delta突变体相比,双重突变体对刚果红(CR),钙氟白(CW)以及细胞团块的敏感性略有提高。但是,在Wt细胞中存在或不存在CR的对数生长期期间,通过Sho1p发生的Cek1p磷酸化不需要Chk1p。这些数据表明Chk1p和Sho1p是平行但独立的信号通路的组成部分。另外,通过GLC / MS和GPC MALLS和NMR分析了菌株的大部分甘露聚糖。与Wt和包含高,中和低Mw甘露聚糖种的CHK1基因重组菌株(CHK23)相比,我们发现菌株CHK21(chk1 Delta null),cek1 Delta null和double突变体的甘露聚糖仅由以下组成:低分子量甘露聚糖。 sho1 Delta null突变体仅表现出甘露聚糖减少的中间类型。缺少高和中等Mw甘露聚糖的cek1 Delta,chk1 Delta和双sho1 / chk1 Delta无突变体的Alcian蓝结合低于仅部分损失了中等Mw甘露聚糖的sho1 Delta无。我们得出结论,Chk1p HK是功能相似但与Sho1p-Cek1p途径平行的途径的一部分,该途径赋予了对细胞壁抑制剂CR和CW的抗性。但是,在Chk1p和Cek1p的甘露聚糖生物合成中存在功能关系,仅部分需要Sho1p。

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