Department of Biology, Concordia University, Montreal, QC H4B 1R6, Canada.
Centre for Microscopy and Cellular Imaging, Department of Biology, Concordia University, Montreal, QC H4B 1R6, Canada.
Genetics. 2022 Jan 4;220(1). doi: 10.1093/genetics/iyab155.
Zinc cluster transcription factors (TFs) are essential fungal regulators of gene expression. In the pathogen Candida albicans, the gene orf19.1604 encodes a zinc cluster TF regulating filament development. Hyperactivation of orf19.1604, which we have named RHA1 for Regulator of Hyphal Activity, generates wrinkled colony morphology under nonhyphal growth conditions, triggers filament formation, invasiveness, and enhanced biofilm formation and causes reduced virulence in the mouse model of systemic infection. The strain expressing activated Rha1 shows up-regulation of genes required for filamentation and cell-wall-adhesion-related proteins. Increased expression is also seen for the hyphal-inducing TFs Brg1 and Ume6, while the hyphal repressor Nrg1 is downregulated. Inactivation of RHA1 reduces filamentation under a variety of filament-inducing conditions. In contrast to the partial effect of either single mutant, the double rha1 ume6 mutant strain is highly defective in both serum- and Spider-medium-stimulated hyphal development. While the loss of Brg1 function blocks serum-stimulated hyphal development, this block can be significantly bypassed by Rha1 hyperactivity, and the combination of Rha1 hyperactivity and serum addition can generate significant polarization even in brg1 ume6 double mutants. Thus, in response to external signals, Rha1 functions with other morphogenesis regulators including Brg1 and Ume6, to mediate filamentation.
锌簇转录因子(TFs)是真菌基因表达的重要调控因子。在病原体白念珠菌中,orf19.1604 基因编码一种锌簇 TF,调节菌丝发育。orf19.1604 的过度激活,我们将其命名为 RHA1(菌丝活性调控因子),在非菌丝生长条件下产生皱缩的菌落形态,触发菌丝形成、侵袭和增强生物膜形成,并导致系统性感染小鼠模型中的毒力降低。表达激活的 Rha1 的菌株表现出对菌丝形成和细胞壁粘附相关蛋白所需基因的上调。菌丝诱导 TF Brg1 和 Ume6 的表达也增加,而菌丝抑制因子 Nrg1 下调。在各种诱导菌丝形成的条件下,RHA1 的失活减少了菌丝形成。与单个突变体的部分效应相反,rha1 ume6 双突变体菌株在血清和蜘蛛培养基刺激的菌丝发育方面高度缺陷。虽然 Brg1 功能的丧失阻止了血清刺激的菌丝发育,但 Rha1 的过度活跃可以显著绕过这种阻断,并且 Rha1 过度活跃和添加血清的组合甚至可以在 brg1 ume6 双突变体中产生显著的极化。因此,响应外部信号,Rha1 与其他形态发生调节剂(包括 Brg1 和 Ume6)一起发挥作用,介导菌丝形成。