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酿酒酵母中纺锤体组装和DNA损伤检查点在细胞周期对染色体改变的反应中的重叠作用。

Overlapping roles of the spindle assembly and DNA damage checkpoints in the cell-cycle response to altered chromosomes in Saccharomyces cerevisiae.

作者信息

Garber Peter M, Rine Jasper

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley, California 94720, USA.

出版信息

Genetics. 2002 Jun;161(2):521-34. doi: 10.1093/genetics/161.2.521.

Abstract

The MAD2-dependent spindle checkpoint blocks anaphase until all chromosomes have achieved successful bipolar attachment to the mitotic spindle. The DNA damage and DNA replication checkpoints block anaphase in response to DNA lesions that may include single-stranded DNA and stalled replication forks. Many of the same conditions that activate the DNA damage and DNA replication checkpoints also activated the spindle checkpoint. The mad2Delta mutation partially relieved the arrest responses of cells to mutations affecting the replication proteins Mcm3p and Pol1p. Thus a previously unrecognized aspect of spindle checkpoint function may be to protect cells from defects in DNA replication. Furthermore, in cells lacking either the DNA damage or the DNA replication checkpoints, the spindle checkpoint contributed to the arrest responses of cells to the DNA-damaging agent methyl methanesulfonate, the replication inhibitor hydroxyurea, and mutations affecting Mcm2p and Orc2p. Thus the spindle checkpoint was sensitive to a wider range of chromosomal perturbations than previously recognized. Finally, the DNA replication checkpoint did not contribute to the arrests of cells in response to mutations affecting ORC, Mcm proteins, or DNA polymerase delta. Thus the specificity of this checkpoint may be more limited than previously recognized.

摘要

依赖MAD2的纺锤体检查点会阻止后期的发生,直到所有染色体都成功地双极附着于有丝分裂纺锤体。DNA损伤和DNA复制检查点会因可能包括单链DNA和停滞的复制叉的DNA损伤而阻止后期的发生。许多激活DNA损伤和DNA复制检查点的相同条件也会激活纺锤体检查点。mad2Delta突变部分缓解了细胞对影响复制蛋白Mcm3p和Pol1p的突变的停滞反应。因此,纺锤体检查点功能中一个以前未被认识到的方面可能是保护细胞免受DNA复制缺陷的影响。此外,在缺乏DNA损伤或DNA复制检查点的细胞中,纺锤体检查点有助于细胞对DNA损伤剂甲磺酸甲酯、复制抑制剂羟基脲以及影响Mcm2p和Orc2p的突变的停滞反应。因此,纺锤体检查点对比以前认识到的更广泛的染色体扰动敏感。最后,DNA复制检查点对影响ORC、Mcm蛋白或DNA聚合酶δ的突变所导致的细胞停滞没有作用。因此,这个检查点的特异性可能比以前认识到的更有限。

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