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Chk1 通路是在细胞周期停滞于“起始点”后防止有丝分裂所必需的。

The chk1 pathway is required to prevent mitosis following cell-cycle arrest at 'start'.

作者信息

Carr A M, Moudjou M, Bentley N J, Hagan I M

机构信息

MRC Cell Mutation Unit, Sussex University, Falmer, UK.

出版信息

Curr Biol. 1995 Oct 1;5(10):1179-90. doi: 10.1016/s0960-9822(95)00234-x.

Abstract

BACKGROUND

The G2-M-phase transition is controlled by cell-cycle checkpoint pathways which inhibit mitosis if previous events are incomplete or if the DNA is damaged. Genetic analyses in yeast have defined two related, but distinct, pathways which prevent mitosis--one which acts when S phase is inhibited, and one which acts when the DNA is damaged. In the fission yeast Schizosaccharomyces pombe, many of the gene products involved have been identified. Six 'radiation checkpoint' (rad) gene products are required for both the S-M and DNA-damage checkpoints, whereas Chk1, a putative protein kinase, is required only for the DNA-damage checkpoint and not for the S-M checkpoint following the inhibition of DNA synthesis.

RESULTS

We have genetically defined a third mitotic control checkpoint pathway in fission yeast which prevents mitosis when passage through 'start' (the commitment point in G1) is compromized. In cycling cells arrested at start, mitosis is prevented by a Chk1-dependent pathway. In the absence of Chk1, G1 cells attempt an abortive mitosis with a 1C DNA content without entering S phase. Similar results are seen in the absence of Rad17, a typical example of a rad gene product.

CONCLUSIONS

Genetic dissection of checkpoints in logarithmically growing fission yeast has identified a pathway that couples mitosis to correct passage through start. This pathway is related to the DNA-structure check-points which ensure that mitosis is dependent on the completion of replication and the integrity of the DNA. We propose that all three mitotic control checkpoints monitor distinct DNA or protein structures at different stages in the cell cycle.

摘要

背景

G2-M期转换由细胞周期检查点通路控制,如果先前的事件未完成或DNA受损,该通路会抑制有丝分裂。酵母中的遗传分析确定了两条相关但不同的阻止有丝分裂的通路——一条在S期受到抑制时起作用,另一条在DNA受损时起作用。在裂殖酵母粟酒裂殖酵母中,许多相关的基因产物已被鉴定出来。S-M检查点和DNA损伤检查点都需要六种“辐射检查点”(rad)基因产物,而推定的蛋白激酶Chk1仅在DNA损伤检查点中需要,在DNA合成受到抑制后的S-M检查点中则不需要。

结果

我们通过遗传学方法在裂殖酵母中定义了第三条有丝分裂控制检查点通路,该通路在通过“起始点”(G1期的承诺点)受到损害时阻止有丝分裂。在停滞于起始点的循环细胞中,有丝分裂通过一条依赖Chk1的通路被阻止。在没有Chk1的情况下,G1期细胞试图进行一次具有1C DNA含量的失败有丝分裂,而不进入S期。在没有Rad17(一种典型的rad基因产物)的情况下也观察到了类似的结果。

结论

对数生长的裂殖酵母中检查点的遗传学剖析确定了一条将有丝分裂与正确通过起始点相耦合的通路。这条通路与DNA结构检查点相关,后者确保有丝分裂依赖于复制的完成和DNA的完整性。我们提出,所有三个有丝分裂控制检查点在细胞周期的不同阶段监测不同的DNA或蛋白质结构。

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