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粟酒裂殖酵母Pmr1p对细胞壁完整性至关重要,是极化细胞生长和胞质分裂所必需的。

Schizosaccharomyces pombe Pmr1p is essential for cell wall integrity and is required for polarized cell growth and cytokinesis.

作者信息

Cortés Juan Carlos G, Katoh-Fukui Reiko, Moto Kanako, Ribas Juan Carlos, Ishiguro Junpei

机构信息

Department of Biology, Faculty of Science and Engineering, Konan University, Okamoto 8-9-1, Kobe 658-8501, Japan.

出版信息

Eukaryot Cell. 2004 Oct;3(5):1124-35. doi: 10.1128/EC.3.5.1124-1135.2004.

Abstract

The cps5-138 fission yeast mutant shows an abnormal lemon-like morphology at 28 degrees C in minimal medium and a lethal thermosensitive phenotype at 37 degrees C. Cell growth is completely inhibited at 28 degrees C in a Ca2+-free medium, in which the wild type is capable of growing normally. Under these conditions, actin patches become randomly distributed throughout the cell, and defects in septum formation and subsequent cytokinesis appear. The mutant cell is hypersensitive to the cell wall-digesting enzymatic complex Novozym234 even under permissive conditions. The gene SPBC31E1.02c, which complements all the mutant phenotypes described above, was cloned and codes for the Ca2+-ATPase homologue Pmr1p. The gene is not essential under optimal growth conditions but is required under conditions of low Ca2+ (<0.1 mM) or high temperature (>35 degrees C). The green fluorescent protein-tagged Cps5 proteins, which are expressed under physiological conditions (an integrated single copy with its own promoter in the cps5Delta strain), display a localization pattern typical of endoplasmic reticulum proteins. Biochemical analyses show that 1,3-beta-D-glucan synthase activity in the mutant is decreased to nearly half that of the wild type and that the mutant cell wall contains no detectable galactomannan when the cells are exposed to a Ca2+-free medium. The mutant acid phosphatase has an increased electrophoretic mobility, suggesting that incomplete protein glycosylation takes place in the mutant cells. These results indicate that S. pombe Pmr1p is essential for the maintenance of cell wall integrity and cytokinesis, possibly by allowing protein glycosylation and the polarized actin distribution to take place normally. Disruption and complementation analyses suggest that Pmr1p shares its function with a vacuolar Ca2+-ATPase homologue, Pmc1p (SPAPB2B4.04c), to prevent lethal activation of calcineurin for cell growth.

摘要

裂殖酵母cps5 - 138突变体在28℃的基本培养基中呈现异常的柠檬状形态,在37℃具有致死性热敏表型。在无Ca2 +的培养基中,28℃时细胞生长完全受到抑制,而野生型在此条件下能够正常生长。在这些条件下,肌动蛋白斑在整个细胞中随机分布,出现隔膜形成及随后胞质分裂的缺陷。即使在允许条件下,突变细胞对细胞壁消化酶复合物诺维信234也高度敏感。克隆了能互补上述所有突变表型的基因SPBC31E1.02c,其编码Ca2 + - ATP酶同源物Pmr1p。该基因在最佳生长条件下并非必需,但在低Ca2 +(<0.1 mM)或高温(>35℃)条件下是必需的。在生理条件下(在cps5Delta菌株中以单拷贝整合并带有自身启动子)表达的绿色荧光蛋白标记的Cps5蛋白呈现出内质网蛋白典型的定位模式。生化分析表明,当细胞暴露于无Ca2 +的培养基中时,突变体中1,3 - β - D - 葡聚糖合酶活性降至野生型的近一半,且突变体细胞壁中未检测到半乳甘露聚糖。突变体酸性磷酸酶的电泳迁移率增加,表明突变体细胞中发生了不完全的蛋白质糖基化。这些结果表明,粟酒裂殖酵母Pmr1p可能通过使蛋白质糖基化和肌动蛋白正常极化分布,对维持细胞壁完整性和胞质分裂至关重要。破坏和互补分析表明,Pmr1p与液泡Ca2 + - ATP酶同源物Pmc1p(SPAPB2B4.04c)共同发挥功能,以防止钙调神经磷酸酶对细胞生长的致死性激活。

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