García-Sánchez Susana, Mavor Abigail L, Russell Claire L, Argimon Silvia, Dennison Paul, Enjalbert Brice, Brown Alistair J P
Aberdeen Fungal Group, School of Medical Sciences, University of Aberdeen, Institute of Medical Sciences, Foresterhill, Aberdeen AB25 2ZD, United Kingdom.
Mol Biol Cell. 2005 Jun;16(6):2913-25. doi: 10.1091/mbc.e05-01-0071. Epub 2005 Apr 6.
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.
在出芽酵母中,Tup1和Ssn6/Cyc8形成一种共抑制因子,调控大量基因。这种Tup1-Ssn6共抑制因子似乎从酵母到人类都保守存在。在致病真菌白色念珠菌中,Tup1调控细胞形态发生、表型转换和代谢,但Ssn6的作用仍不清楚。我们发现白色念珠菌ssn6和tup1突变体在形态和侵袭表型上存在明显差异。与Tup1不同,Ssn6缺失促进了类似于表型转换的形态学事件,而不是丝状生长。转录谱分析显示Ssn6和Tup1调控子之间的重叠极少。在研究的条件下,被Tup1和Nrg1抑制的菌丝特异性基因在ssn6细胞中并未去抑制。相反,阶段特异性基因WH11在ssn6细胞中去抑制,但在tup1或nrg1细胞中没有。因此,Ssn6和Tup1在白色念珠菌中发挥不同作用。然而,Ssn6和Tup1都是Nrg1介导的人工NRE启动子抑制以及白色念珠菌单杂交系统中LexA-Nrg1介导的抑制所必需的。这些观察结果在与出芽酵母中Tup1-Ssn6范式总体一致的模型中得到了解释。