Bharat Chattoo Genome Research Centre, Department of Microbiology and Biotechnology Centre, Faculty of Science, The Maharaja Sayajirao University of Baroda, Vadodara, 390002, Gujarat, India.
Department of Microbiology and Biotechnology Centre, Faculty of Science, The Maharaja Sayajirao University of Baroda, Vadodara, 390002, Gujarat, India.
Int Microbiol. 2022 Nov;25(4):789-802. doi: 10.1007/s10123-022-00264-7. Epub 2022 Jul 12.
Eukaryotic cells respond to environmental cues through mitogen activated protein kinase (MAPK) signaling pathways. Each MAPK cascade is specific to particular stimuli and mediates specialized responses through activation of transcription factors. In the budding yeast, Saccharomyces cerevisiae, the pheromone-induced mating pathway and the starvation-responsive invasive growth/filamentation pathway generate their distinct outputs through the transcription factors Ste12 and Tec1, respectively. In this study, we report the functional characterization of these transcription factors in the closely related human opportunistic pathogenic yeast Candida glabrata. Two homologues each for S. cerevisiae TEC1 and STE12 were identified in C. glabrata. Both C. glabrata Tec1 proteins contain the N-terminal TEA DNA-binding domain characteristic of the TEA/ATTS transcription factor family. Similarly, the DNA-binding homeodomain shared by members of the highly conserved fungal Ste12 transcription factor family is present in N-terminus of both C. glabrata Ste12 transcription factors. We show that both C. glabrata STE12 genes are at least partial functional orthologues of S. cerevisiae STE12 as they can rescue the mating defect of haploid S. cerevisiae ste12 null mutant. Knockout of one of the STE12 genes (ORF CAGL0H02145g) leads to decreased biofilm development; a stronger biofilm-impaired phenotype results from loss of both CgSTE12 genes in the double deletion mutant (Cgste12ΔΔ). The transcript levels of one of the TEC1 genes (ORF CAGL0M01716g) were found to be upregulated upon exposure to low pH; its deletion causes slightly increased sensitivity to higher concentrations of acetic acid. Heat shock leads to increase in mRNA levels of one of the STE12 genes (ORF CAGL0M01254g). These findings suggest a role of Tec1 and Ste12 transcription factors in the regulation of some traits (biofilm formation, response to low pH stress and elevated temperature) that contribute to C. glabrata's ability to colonize various host niches and to occasionally cause disease.
真核细胞通过丝裂原活化蛋白激酶 (MAPK) 信号通路对环境信号作出反应。每条 MAPK 级联反应都针对特定的刺激,并通过激活转录因子来介导特定的反应。在出芽酵母酿酒酵母中,交配途径和饥饿响应的侵袭生长/丝状生长途径通过转录因子 Ste12 和 Tec1 分别产生其独特的输出。在这项研究中,我们报告了这些转录因子在密切相关的人类机会致病性酵母 Candida glabrata 中的功能特征。在 C. glabrata 中鉴定出酿酒酵母 TEC1 和 STE12 的每个对应物的两个同源物。C. glabrata Tec1 蛋白都包含 TEA/ATTS 转录因子家族特征的 N 端 TEA DNA 结合域。同样,高度保守的真菌 Ste12 转录因子家族成员共有的 DNA 结合同源结构域存在于 C. glabrata Ste12 转录因子的 N 端。我们表明,C. glabrata STE12 基因至少是酿酒酵母 STE12 的部分功能同源物,因为它们可以挽救酿酒酵母 ste12 缺失突变体的交配缺陷。敲除一个 STE12 基因(ORF CAGL0H02145g)导致生物膜发育减少;在双缺失突变体(Cgste12ΔΔ)中失去两个 CgSTE12 基因会导致更强的生物膜受损表型。暴露于低 pH 值会导致一个 Tec1 基因(ORF CAGL0M01716g)的转录水平上调;其缺失会导致对更高浓度的乙酸略微增加敏感性。热应激导致一个 STE12 基因(ORF CAGL0M01254g)的 mRNA 水平增加。这些发现表明 Tec1 和 Ste12 转录因子在调节一些特征(生物膜形成、对低 pH 应激和高温的反应)方面发挥作用,这些特征有助于 C. glabrata 定植各种宿主小生境并偶尔引起疾病的能力。