Lee Hye-Jeong, Kim Jong-Myeong, Kang Woo Kyu, Yang Heebum, Kim Jeong-Yoon
Department of Microbiology and Molecular Biology, College of Bioscience and Biotechnology, Chungnam National University, Daejeon, Republic of Korea.
Department of Microbiology and Molecular Biology, College of Bioscience and Biotechnology, Chungnam National University, Daejeon, Republic of Korea
Eukaryot Cell. 2015 Jul;14(7):671-83. doi: 10.1128/EC.00016-15. Epub 2015 May 22.
NDR (nuclear Dbf2-related) kinases are essential components for polarized morphogenesis, cytokinesis, cell proliferation, and apoptosis. The NDR kinase Cbk1 is required for the hyphal growth of Candida albicans; however, the molecular functions of Cbk1 in hyphal morphogenesis are largely unknown. Here, we report that Cbk1 downregulates the transcriptional repressor Nrg1 through the mRNA-binding protein Ssd1, which has nine Cbk1 phosphorylation consensus motifs. We found that deletion of SSD1 partially suppressed the defective hyphal growth of the C. albicans cbk1Δ/Δ mutant and that Ssd1 physically interacts with Cbk1. Cbk1 was required for Ssd1 localization to polarized growth sites. The phosphomimetic SSD1 allele (ssd1-9E) allowed the cbk1Δ/Δ mutant to form short hyphae, and the phosphodeficient SSD1 allele (ssd1-9A) resulted in shorter hyphae than did the wild-type SSD1 allele, indicating that Ssd1 phosphorylation by Cbk1 is important for hyphal morphogenesis. Furthermore, we show that the transcriptional repressor Nrg1 does not disappear during hyphal initiation in the cbk1Δ/Δ mutant but is completely absent in the cbk1Δ/Δ ssd1Δ/Δ double mutant. Deletion of SSD1 also increased Als3 expression and internalization of the cbk1Δ/Δ mutant in the human embryonic kidney cell line HEK293T. Collectively, our results suggest that one of the functions of Cbk1 in the hyphal morphogenesis of C. albicans is to downregulate Nrg1 through Ssd1.
NDR(核Dbf2相关)激酶是极化形态发生、胞质分裂、细胞增殖和细胞凋亡的重要组成部分。NDR激酶Cbk1是白色念珠菌菌丝生长所必需的;然而,Cbk1在菌丝形态发生中的分子功能在很大程度上尚不清楚。在此,我们报告Cbk1通过具有九个Cbk1磷酸化共有基序的mRNA结合蛋白Ssd1下调转录抑制因子Nrg1。我们发现缺失SSD1部分抑制了白色念珠菌cbk1Δ/Δ突变体有缺陷的菌丝生长,并且Ssd1与Cbk1发生物理相互作用。Cbk1是Ssd1定位于极化生长位点所必需的。模拟磷酸化的SSD1等位基因(ssd1-9E)使cbk1Δ/Δ突变体形成短菌丝,而磷酸缺陷型SSD1等位基因(ssd1-9A)导致的菌丝比野生型SSD1等位基因的更短,表明Cbk1对Ssd1的磷酸化对于菌丝形态发生很重要。此外,我们表明转录抑制因子Nrg1在cbk1Δ/Δ突变体的菌丝起始过程中不会消失,但在cbk1Δ/Δ ssd1Δ/Δ双突变体中完全不存在。缺失SSD1也增加了cbk1Δ/Δ突变体在人胚肾细胞系HEK293T中的Als3表达和内化。总的来说,我们的结果表明Cbk1在白色念珠菌菌丝形态发生中的功能之一是通过Ssd1下调Nrg1。