School of Medical Sciences, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen, AB25 2ZD, Scotland, UK.
J Cell Sci. 2010 Jul 1;123(Pt 13):2199-206. doi: 10.1242/jcs.060210. Epub 2010 Jun 8.
The ability to undergo polarised cell growth is fundamental to the development of almost all walled organisms. Fungi are characterised by yeasts and moulds, and both cellular forms have been studied extensively as tractable models of cell polarity. Chitin is a hallmark component of fungal cell walls. Chitin synthesis is essential for growth, viability and rescue from many conditions that impair cell-wall integrity. In the polymorphic human pathogen Candida albicans, chitin synthase 3 (Chs3) synthesises the majority of chitin in the cell wall and is localised at the tips of growing buds and hyphae, and at the septum. An analysis of the C. albicans phospho-proteome revealed that Chs3 can be phosphorylated at Ser139. Mutation of this site showed that both phosphorylation and dephosphorylation are required for the correct localisation and function of Chs3. The kinase Pkc1 was not required to target Chs3 to sites of polarised growth. This is the first report demonstrating an essential role for chitin synthase phosphorylation in the polarised biosynthesis of fungal cell walls and suggests a new mechanism for the regulation of this class of glycosyl-transferase enzyme.
能够进行极化细胞生长是几乎所有有壁生物发育的基础。真菌的特征是酵母和霉菌,这两种细胞形式都被广泛研究为细胞极性的可处理模型。几丁质是真菌细胞壁的标志性成分。几丁质合成对于生长、活力和从许多破坏细胞壁完整性的条件中恢复至关重要。在多态性的人体病原体白色念珠菌中,几丁质合酶 3(Chs3)在细胞壁中合成大部分几丁质,定位于生长芽和菌丝的尖端以及隔膜处。对白色念珠菌磷酸化蛋白质组的分析表明,Chs3 可以在 Ser139 处被磷酸化。该位点的突变表明,磷酸化和去磷酸化对于 Chs3 的正确定位和功能都是必需的。激酶 Pkc1 不需要将 Chs3 靶向到极化生长的部位。这是首次报道几丁质合酶磷酸化在真菌细胞壁的极化生物合成中起重要作用,并为这类糖基转移酶的调控提出了一种新的机制。