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酿酒酵母中特定的早期G1期阻滞伴随着严格反应,导致细胞在静止状态下生长停滞,类似于高等真核生物的G0期。

Specific early-G1 blocks accompanied with stringent response in Saccharomyces cerevisiae lead to growth arrest in resting state similar to the G0 of higher eucaryotes.

作者信息

Iida H, Yahara I

出版信息

J Cell Biol. 1984 Apr;98(4):1185-93. doi: 10.1083/jcb.98.4.1185.

Abstract

Growth arrests of Saccharomyces cerevisiae cells in early G1 phase brought by various means were classified into two types according to the mode of growth recovery after release of the restraints against growth. The first type, including arrests caused by cdc25, cdc33, cdc35, and ils1 mutations at the nonpermissive temperature and also by sulfur starvation, showed a subsequent delay in the onset of budding when shifted back to permissive conditions. The length of the delay was positively correlated with the time that cells had been arrested. The second type, including those caused by cdc28 and cdc24 mutations and by alpha factor, did not affect the mode of growth recovery after the shift to permissive conditions irrespective of the time that cell proliferation had been restricted. Growth arrests of the first type seem to allow yeast cells to enter a resting state equivalent to the G0 state of higher eucaryotes because features of the G0 shown with lymphocytes and other cultured cells including unusually long delay before the growth recovery (L.H. Augenlicht and R. Baserga, 1974, Exp. Cell Res., 89:255-262; and Kumagai, J., H. Akiyama, S. Iwashita, H. lida, and I. Yahara, 1981, J. Immunol., 126:1249-1254) appeared to be associated with this type. We have noted that arrests of the first type were always accompanied with a stringent response of macromolecular synthesis and its partial release by cycloheximide. Mapping of arrest points along the path of the cell cycle by the reciprocal shift experiment suggested that arrest points in G1 that led to the G0-like arrest precede or are near the step sensitive to alpha-factor.

摘要

通过各种方式使酿酒酵母细胞在G1早期阶段生长停滞,根据解除生长限制后生长恢复的模式,可将其分为两种类型。第一种类型,包括在非允许温度下由cdc25、cdc33、cdc35和ils1突变以及硫饥饿导致的生长停滞,当转移回允许条件时,随后出芽起始会延迟。延迟的长度与细胞停滞的时间呈正相关。第二种类型,包括由cdc28和cdc24突变以及α因子导致的生长停滞,无论细胞增殖受限的时间长短,转移到允许条件后均不影响生长恢复模式。第一种类型的生长停滞似乎使酵母细胞进入了一种与高等真核生物的G0状态相当的静止状态,因为淋巴细胞和其他培养细胞所表现出的G0特征,包括生长恢复前异常长的延迟(L.H.奥根利希特和R.巴塞尔加,1974年,《实验细胞研究》,89:255 - 262;熊谷纯、秋山博、岩下幸司、饭田浩、矢原一,1981年,《免疫学杂志》,126:1249 - 1254)似乎与这种类型相关。我们注意到,第一种类型的停滞总是伴随着大分子合成的严格反应以及放线菌酮对其的部分解除。通过双向转移实验沿细胞周期路径绘制停滞点表明,导致类G0停滞的G1期停滞点先于或接近对α因子敏感的步骤。

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