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Global Roles of Ssn6 in Tup1- and Nrg1-dependent Gene Regulation in the Fungal Pathogen, Candida albicans

机译:Ssn6在真菌病原体,白色念珠菌中的Tup1和Nrg1依赖性基因调节中的全局作用。

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In budding yeast, Tup1 and Ssn6/Cyc8 form a corepressor that regulates a large number of genes. This Tup1-Ssn6 corepressor appears to be conserved from yeast to man. In the pathogenic fungus Candida albicans , Tup1 regulates cellular morphogenesis, phenotypic switching, and metabolism, but the role of Ssn6 remains unclear. We show that there are clear differences in the morphological and invasive phenotypes of C. albicans ssn6 and tup1 mutants. Unlike Tup1, Ssn6 depletion promoted morphological events reminiscent of phenotypic switching rather than filamentous growth. Transcript profiling revealed minimal overlap between the Ssn6 and Tup1 regulons. Hypha-specific genes, which are repressed by Tup1 and Nrg1, were not derepressed in ssn6 cells under the conditions studied. In contrast, the phase specific gene WH11 was derepressed in ssn6 cells, but not in tup1 or nrg1 cells. Hence Ssn6 and Tup1 play distinct roles in C. albicans. Nevertheless, both Ssn6 and Tup1 were required for the Nrg1-mediated repression of an artificial NRE promoter, and lexA-Nrg1 mediated repression in the C. albicans one-hybrid system. These observations are explained in models that are generally consistent with the Tup1-Ssn6 paradigm in budding yeast.
机译:在出芽的酵母中,Tup1和Ssn6 / Cyc8形成了一个调控大量基因的共加压子。这种Tup1-Ssn6核心表达因子似乎从酵母到人都是保守的。在致病性真菌白色念珠菌中,Tup1调节细胞形态发生,表型转换和代谢,但Ssn6的作用仍不清楚。我们显示,在白色念珠菌ssn6和tup1突变体的形态和侵入表型上有明显的差异。与Tup1不同,Ssn6耗竭促进了形态事件,使人联想到表型转换而不是丝状生长。成绩单分析显示Ssn6和Tup1调节子之间的重叠最小。由Tup1和Nrg1抑制的菌丝特异性基因在所研究的条件下不会在ssn6细胞中被抑制。相反,在ssn6细胞中,相特异性基因WH11被抑制,而在tup1或nrg1细胞中则不被抑制。因此,Ssn6和Tup1在白色念珠菌中起不同的作用。但是,Ssn6和Tup1都是人工NRE启动子的Nrg1介导的阻遏作用和白色念珠菌一杂交系统中lexA-Nrg1介导的阻遏作用所必需的。这些观察结果在模型中得到了解释,该模型通常与发芽酵母中的Tup1-Ssn6范例一致。

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