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Fission Yeast Rho5p GTPase Is a Functional Paralogue of Rho1p That Plays a Role in Survival of Spores and Stationary-Phase Cells

机译:裂变酵母Rho5p GTPase是Rho1p的功能旁系同源物,在孢子和固定相细胞的存活中发挥作用

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摘要

The Rho GTPase family and their effectors are key regulators involved in many eukaryotic cell functions related to actin organization and polarity establishment. Schizosaccharomyces pombe Rho1p is essential, directly activates the (1,3)-β-d-glucan synthase, and participates in regulation of cell wall growth and morphogenesis. Here we describe the characterization of the fission yeast Rho5p GTPase, highly homologous to Rho1p, sharing 86% identity and 95% similarity. Overexpression of the hyperactive allele rho5-G15V causes a morphological effect similar to that of rho1-G15V, but the penetrance is significantly lower, and overexpression of the dominant-negative allele rho5-T20N causes lysis like that of rho1-T20N. Importantly, overexpression of rho5+ but no other rho genes is able to rescue the lethality of rho1Δ cells. Shutoff experiments indicated that Rho5p can replace Rho1p, but it is not as effective in maintaining cell wall integrity or actin organization. rho5+ expression is hardly detected during log-phase growth but is induced under nutritional starvation conditions. rho5Δ cells are viable and do not display any defects during logarithmic growth. However, when rho1+ expression is repressed during stationary phase, rho5Δ cells display reduced viability. Ascospores lacking Rho5p are less resistant to heat or lytic enzymes than wild-type spores. Moreover, h90 mutant strains carrying the hyperactive rho5-G15V or the dominant-negative rho5-T20N alleles display severe ascospore formation defects. These results suggest that Rho5p functions in a way similar to, but less efficient than, Rho1p, plays a nonessential role during stationary phase, and participates in the spore wall formation.
机译:Rho GTPase家族及其效应子是参与许多与肌动蛋白组织和极性建立有关的真核细胞功能的关键调控因子。粟酒裂殖酵母Rho1p是必不可少的,它直接激活(1,3)-β-d-葡聚糖合酶,并参与细胞壁生长和形态发生的调控。在这里,我们描述裂变酵母Rho5p GTPase的表征,与Rho1p高度同源,具有86%的同一性和95%的相似性。高活性等位基因rho5-G15V的过表达引起类似于rho1-G15V的形态学效应,但渗透率明显较低,显性阴性等位基因rho5-T20N的过表达引起像rho1-T20N一样的裂解。重要的是,rho5 +的过​​表达但没有其他rho基因能够挽救rho1Δ细胞的致死性。 Shutoff实验表明Rho5p可以代替Rho1p,但在维持细胞壁完整性或肌动蛋白组织方面不那么有效。在对数生长期几乎未检测到rho5 +表达,但在营养饥饿的条件下被诱导。 rho5Δ细胞是活的,在对数生长过程中不显示任何缺陷。然而,当rho1 +表达在稳定期受到抑制时,rho5Δ细胞显示出降低的生存能力。缺少Rho5p的子囊孢子对热或裂解酶的抵抗力比野生型孢子弱。此外,携带高活性rho5-G15V或显性负性rho5-T20N等位基因的h90突变株显示出严重的子囊孢子形成缺陷。这些结果表明,Rho5p的功能类似于Rho1p,但效率不如Rho1p,在稳定期起着不必要的作用,并参与了孢子壁的形成。

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