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Involvement of Rho-type GTPase in control of cell size in Saccharomyces cerevisiae

机译:Rho型GTPase参与酿酒酵母细胞大小的控制。

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摘要

Maintaining specific cell size, which is important for many organisms, is achieved by coordinating cell growth and cell division. In the budding yeast Saccharomyces cerevisiae, the existence of two cell-size checkpoints is proposed: at the first checkpoint, cell size is monitored before budding at the G(1)/S transition, and at the second checkpoint, actin depolymerization occurring in the small bud is monitored before the G(2)/M transition. Morphological analyses have revealed that the small GTPase Rho1p participates in cell-size control at both the G(1)/S and the G(2)/M boundaries. One group of rho1 mutants (rho1A) underwent premature entry into mitosis, leading to the birth of abnormally small cells. In another group of rho1 mutants (rho1B), the mother cells failed to reach an appropriate size before budding, and expression of the G(1) cyclin Cln2p began at an earlier phase of the cell cycle. Analyses of mutants defective in Rho1p effector proteins indicate that Skn7p, Fks1p and Mpk1p are involved in cell-size control. Thus, Rho1p and its downstream regulatory pathways are involved in controlling cell size in S. cerevisiae.
机译:通过协调细胞生长和细胞分裂,可以维持对许多生物至关重要的特定细胞大小。在萌芽的酿酒酵母中,提出了两个细胞大小的检查点的存在:在第一个检查点,在G(1)/ S过渡出芽之前监测细胞大小,在第二个检查点,在细胞中发生肌动蛋白解聚。在G(2)/ M转换之前监视小芽。形态学分析表明,小的GTPase Rho1p在G(1)/ S和G(2)/ M边界均参与细胞大小控制。一组rho1突变体(rho1A)提前进入有丝分裂状态,导致异常小细胞的诞生。在另一组rho1突变体(rho1B)中,母细胞在出芽前未能达到合适的大小,而G(1)细胞周期蛋白Cln2p的表达始于细胞周期的早期。 Rho1p效应蛋白缺陷突变体的分析表明,Skn7p,Fks1p和Mpk1p参与细胞大小控制。因此,Rho1p及其下游调节途径参与啤酒酵母中细胞大小的控制。

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