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裂殖酵母中DNA合成起始的控制

Control over the onset of DNA synthesis in fission yeast.

作者信息

Simanis V, Hayles J, Nurse P

机构信息

Cell Cycle Control Laboratory, Imperial Cancer Research Fund, Lincoln's Inn Fields, London, U.K.

出版信息

Philos Trans R Soc Lond B Biol Sci. 1987 Dec 15;317(1187):507-16. doi: 10.1098/rstb.1987.0077.

DOI:10.1098/rstb.1987.0077
PMID:2894685
Abstract

The fission yeast Schizosaccharomyces pombe has been used to identify gene functions required for the cell to become committed to the mitotic cell cycle and to initiate the processes leading to chromosome replication in S-phase. Two gene functions cdc2 and cdc10 must be executed for the cell to traverse 'start' and proceed from G1 into S-phase. Before the completion of these two functions the cell is in an uncommitted state and can undergo alternative developmental fates such as conjugation. A third gene, suc1, has also been identified whose product may interact directly with that of cdc2 at 'start'. The molecular functions of the genes involved in the completion of 'start' have been investigated. The cdc2 gene has been shown to be a protein kinase, suggesting that phosphorylation may be involved in the control over the transition from G1 into S-phase. The biochemical functions of the cdc10 and suc1 gene products have not yet been elucidated. A control at 'start' has also been shown to exist in the budding yeast Saccharomyces cerevisiae. Traverse of 'start' requires the execution of the CDC28 gene function. The cdc2 and CDC28 gene products (lower-case letters represent genes of Schizosaccharomyces pombe, and capital letters genes of Saccharomyces cerevisiae) are functionally homologous, suggesting that the processes involved in traverse of 'start' are highly conserved. An analogous control may also exist in the G1 period of mammalian cells, suggesting that the 'start' control step, after which cells become committed to the mitotic cell cycle, may have been conserved through evolution.

摘要

裂殖酵母粟酒裂殖酵母已被用于确定细胞进入有丝分裂细胞周期并启动导致S期染色体复制过程所需的基因功能。细胞要穿过“起始点”并从G1期进入S期,必须执行两种基因功能,即cdc2和cdc10。在完成这两种功能之前,细胞处于未决定状态,可以经历诸如接合等其他发育命运。还鉴定出了第三个基因suc1,其产物可能在“起始点”处与cdc2的产物直接相互作用。已经对参与完成“起始点”的基因的分子功能进行了研究。已证明cdc2基因是一种蛋白激酶,这表明磷酸化可能参与了从G1期到S期过渡的控制。cdc10和suc1基因产物的生化功能尚未阐明。在芽殖酵母酿酒酵母中也已证明存在“起始点”控制。穿过“起始点”需要执行CDC28基因功能。cdc2和CDC28基因产物(小写字母代表粟酒裂殖酵母的基因,大写字母代表酿酒酵母的基因)在功能上是同源的,这表明参与穿过“起始点”的过程高度保守。在哺乳动物细胞的G1期可能也存在类似的控制,这表明细胞进入有丝分裂细胞周期后,“起始点”控制步骤可能在进化过程中得以保留。

相似文献

1
Control over the onset of DNA synthesis in fission yeast.裂殖酵母中DNA合成起始的控制
Philos Trans R Soc Lond B Biol Sci. 1987 Dec 15;317(1187):507-16. doi: 10.1098/rstb.1987.0077.
2
The fission yeast cell cycle control gene cdc2: isolation of a sequence suc1 that suppresses cdc2 mutant function.裂殖酵母细胞周期控制基因cdc2:抑制cdc2突变体功能的suc1序列的分离。
Mol Gen Genet. 1986 Feb;202(2):291-3. doi: 10.1007/BF00331653.
3
Site-specific mutagenesis of cdc2+, a cell cycle control gene of the fission yeast Schizosaccharomyces pombe.粟酒裂殖酵母细胞周期控制基因cdc2⁺的位点特异性诱变
Mol Cell Biol. 1986 Oct;6(10):3523-30. doi: 10.1128/mcb.6.10.3523-3530.1986.
4
Control of DNA synthesis genes in fission yeast by the cell-cycle gene cdc10+.细胞周期基因cdc10 +对裂殖酵母中DNA合成基因的调控
Nature. 1992 Jan 30;355(6359):449-53. doi: 10.1038/355449a0.
5
Cloning, sequencing and transcriptional control of the Schizosaccharomyces pombe cdc10 'start' gene.粟酒裂殖酵母cdc10“起始”基因的克隆、测序及转录调控
EMBO J. 1985 Feb;4(2):457-63. doi: 10.1002/j.1460-2075.1985.tb03651.x.
6
Characterization of the fission yeast cdc10+ protein that is required for commitment to the cell cycle.
J Cell Sci. 1989 Jan;92 ( Pt 1):51-6. doi: 10.1242/jcs.92.1.51.
7
A B-type cyclin negatively regulates conjugation via interacting with cell cycle 'start' genes in fission yeast.在裂殖酵母中,一种B型细胞周期蛋白通过与细胞周期“起始”基因相互作用来负向调节接合过程。
EMBO J. 1994 Apr 15;13(8):1863-72. doi: 10.1002/j.1460-2075.1994.tb06455.x.
8
res2+, a new member of the cdc10+/SWI4 family, controls the 'start' of mitotic and meiotic cycles in fission yeast.Res2+是cdc10+/SWI4家族的一个新成员,它控制裂殖酵母有丝分裂和减数分裂周期的“起始”。
EMBO J. 1994 Apr 15;13(8):1873-80. doi: 10.1002/j.1460-2075.1994.tb06456.x.
9
Yeast as a model system for understanding the control of DNA replication in Eukaryotes.
Bioessays. 1990 Oct;12(10):457-63. doi: 10.1002/bies.950121002.
10
The Cdc2 protein kinase controls Cdc10/Sct1 complex formation.
Mol Biol Cell. 1997 Jun;8(6):1105-15. doi: 10.1091/mbc.8.6.1105.

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