Nakazawa T, Horiuchi H, Ohta A, Takagi M
Department of Biotechnology, The University of Tokyo, Japan.
J Bacteriol. 1998 Apr;180(8):2079-86. doi: 10.1128/JB.180.8.2079-2086.1998.
Additional copies of the centromeric DNA (CEN) region induce pseudohyphal growth in a dimorphic yeast, Candida maltosa (T. Nakazawa, T. Motoyama, H. Horiuchi, A. Ohta, and M. Takagi, J. Bacteriol. 179:5030-5036, 1997). To understand the mechanism of this transition, we screened the gene library of C. maltosa for sequences which could suppress this morphological change. As a result, we isolated the 5' end of a new gene, EPD1 (for essential for pseudohyphal development), and then cloned the entire gene. The predicted amino acid sequence of Epdlp was highly homologous to those of Ggp1/Gas1/Cwh52p, a glycosylphosphatidylinositol-anchored protein of Saccharomyces cerevisiae, and Phr1p and Phr2p of Candida albicans. The expression of EPD1 was moderately regulated by environmental pH. A homozygous EPD1 null mutant showed some morphological defects and reduction in growth rate and reduced levels of both alkali-soluble and alkali-insoluble beta-glucans. Moreover, the mutant could not undergo the transition from yeast form to pseudohyphal form induced by additional copies of the CEN sequence at pH 4 or by n-hexadecane at pH 4 or pH 7, suggesting that EPD1 is not essential for yeast form growth but is essential for transition to the pseudohyphal form. Overexpression of the amino-terminal part of Epd1p under the control of the GAL promoter suppressed the pseudohyphal development induced by additional copies of the CEN sequence, whereas overexpression of the full-length EPD1 did not. This result and the initial isolation of the 5' end of EPD1 as a suppressor of the pseudohyphal growth induced by the CEN sequence suggest that the amino-terminal part of Epd1p may have a dominant-negative effect on the functions of Epd1p in the pseudohyphal growth induced by the CEN sequence.
着丝粒DNA(CEN)区域的额外拷贝会在二态性酵母麦芽糖假丝酵母中诱导假菌丝生长(T. Nakazawa、T. Motoyama、H. Horiuchi、A. Ohta和M. Takagi,《细菌学杂志》179:5030 - 5036,1997年)。为了理解这种转变的机制,我们在麦芽糖假丝酵母的基因文库中筛选能够抑制这种形态变化的序列。结果,我们分离出了一个新基因EPD1(假菌丝发育必需基因)的5'端,随后克隆了整个基因。Epdlp的预测氨基酸序列与酿酒酵母的糖基磷脂酰肌醇锚定蛋白Ggp1/Gas1/Cwh52p以及白色念珠菌的Phr1p和Phr2p高度同源。EPD1的表达受到环境pH的适度调控。纯合的EPD1缺失突变体表现出一些形态缺陷、生长速率降低以及碱溶性和碱不溶性β - 葡聚糖水平降低。此外,该突变体在pH 4时不能由CEN序列的额外拷贝诱导从酵母形态转变为假菌丝形态,在pH 4或pH 7时也不能由正十六烷诱导转变,这表明EPD1对于酵母形态生长不是必需的,但对于向假菌丝形态的转变是必需的。在GAL启动子控制下,Epd1p氨基末端部分的过表达抑制了由CEN序列额外拷贝诱导的假菌丝发育,而全长EPD1的过表达则没有。这一结果以及最初将EPD1的5'端作为CEN序列诱导的假菌丝生长的抑制子分离出来,表明Epd1p的氨基末端部分可能对Epd1p在CEN序列诱导的假菌丝生长中的功能具有显性负效应。