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2
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A network of transcription factors in complex with a regulating cell cycle cyclin orchestrates fungal oxidative stress responses.一个与调控细胞周期细胞周期蛋白复合物的转录因子网络协调真菌的氧化应激反应。
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本文引用的文献

1
Genetic Control of the Cell Division Cycle in Yeast: V. Genetic Analysis of cdc Mutants.酵母细胞分裂周期的遗传控制:V. cdc 突变体的遗传分析。
Genetics. 1973 Jun;74(2):267-86. doi: 10.1093/genetics/74.2.267.
2
A new gene affecting the efficiency of mating-type interconversions in homothallic strains of Saccharomyces cerevisiae.一个影响酿酒酵母同宗配合菌株中交配型相互转换效率的新基因。
Genetics. 1977 Sep;87(1):33-50. doi: 10.1093/genetics/87.1.33.
3
Functional analysis of the Saccharomyces cerevisiae UBC11 gene.酿酒酵母UBC11基因的功能分析。
Yeast. 1998 Jun 15;14(8):747-57. doi: 10.1002/(SICI)1097-0061(19980615)14:8<747::AID-YEA271>3.0.CO;2-T.
4
MPF localization is controlled by nuclear export.成熟促进因子(MPF)的定位受核输出调控。
EMBO J. 1998 Jul 15;17(14):4127-38. doi: 10.1093/emboj/17.14.4127.
5
CDC16 controls initiation at chromosome replication origins.细胞分裂周期蛋白16(CDC16)控制染色体复制起点的起始。
Mol Cell. 1998 Feb;1(3):457-63. doi: 10.1016/s1097-2765(00)80046-5.
6
The regulation of Cdc20 proteolysis reveals a role for APC components Cdc23 and Cdc27 during S phase and early mitosis.Cdc20蛋白水解的调控揭示了后期促进复合物组分Cdc23和Cdc27在S期和有丝分裂早期的作用。
Curr Biol. 1998 Jun 18;8(13):750-60. doi: 10.1016/s0960-9822(98)70298-2.
7
A role for NIMA in the nuclear localization of cyclin B in Aspergillus nidulans.NIMA在构巢曲霉细胞周期蛋白B核定位中的作用。
J Cell Biol. 1998 Jun 29;141(7):1575-87. doi: 10.1083/jcb.141.7.1575.
8
Cyclin-specific START events and the G1-phase specificity of arrest by mating factor in budding yeast.芽殖酵母中细胞周期蛋白特异性的起始事件以及交配因子对G1期停滞的特异性
Mol Gen Genet. 1998 May;258(3):183-98. doi: 10.1007/s004380050722.
9
Combinatorial control in ubiquitin-dependent proteolysis: don't Skp the F-box hypothesis.泛素依赖性蛋白水解中的组合控制:不要忽视F-box假说。
Trends Genet. 1998 Jun;14(6):236-43. doi: 10.1016/s0168-9525(98)01473-5.
10
Pheromone-dependent G1 cell cycle arrest requires Far1 phosphorylation, but may not involve inhibition of Cdc28-Cln2 kinase, in vivo.在体内,信息素依赖的G1期细胞周期停滞需要Far1磷酸化,但可能不涉及对Cdc28-Cln2激酶的抑制。
Mol Cell Biol. 1998 Jul;18(7):3681-91. doi: 10.1128/MCB.18.7.3681.

酿酒酵母细胞周期中Cdc28细胞周期蛋白依赖性蛋白激酶活性的调控

Regulation of Cdc28 cyclin-dependent protein kinase activity during the cell cycle of the yeast Saccharomyces cerevisiae.

作者信息

Mendenhall M D, Hodge A E

机构信息

L. P. Markey Cancer Center, University of Kentucky, Lexington, Kentucky 40536-0096, USA.

出版信息

Microbiol Mol Biol Rev. 1998 Dec;62(4):1191-243. doi: 10.1128/MMBR.62.4.1191-1243.1998.

DOI:10.1128/MMBR.62.4.1191-1243.1998
PMID:9841670
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC98944/
Abstract

The cyclin-dependent protein kinase (CDK) encoded by CDC28 is the master regulator of cell division in the budding yeast Saccharomyces cerevisiae. By mechanisms that, for the most part, remain to be delineated, Cdc28 activity controls the timing of mitotic commitment, bud initiation, DNA replication, spindle formation, and chromosome separation. Environmental stimuli and progress through the cell cycle are monitored through checkpoint mechanisms that influence Cdc28 activity at key cell cycle stages. A vast body of information concerning how Cdc28 activity is timed and coordinated with various mitotic events has accrued. This article reviews that literature. Following an introduction to the properties of CDKs common to many eukaryotic species, the key influences on Cdc28 activity-cyclin-CKI binding and phosphorylation-dephosphorylation events-are examined. The processes controlling the abundance and activity of key Cdc28 regulators, especially transcriptional and proteolytic mechanisms, are then discussed in detail. Finally, the mechanisms by which environmental stimuli influence Cdc28 activity are summarized.

摘要

由CDC28编码的细胞周期蛋白依赖性蛋白激酶(CDK)是芽殖酵母酿酒酵母中细胞分裂的主要调节因子。通过在很大程度上仍有待阐明的机制,Cdc28活性控制有丝分裂承诺的时间、芽的起始、DNA复制、纺锤体形成和染色体分离。通过在关键细胞周期阶段影响Cdc28活性的检查点机制来监测环境刺激和细胞周期进程。关于Cdc28活性如何定时以及与各种有丝分裂事件协调的大量信息已经积累起来。本文对该文献进行综述。在介绍了许多真核生物共有的CDK特性之后,研究了对Cdc28活性的关键影响——细胞周期蛋白-CKI结合以及磷酸化-去磷酸化事件。然后详细讨论了控制关键Cdc28调节因子丰度和活性的过程,特别是转录和蛋白水解机制。最后,总结了环境刺激影响Cdc28活性的机制。