Cell Cycle Checkpoint in Response to DNA Damage

DNA 损伤反应中的细胞周期检查点

• 批准号: 6828679
• 负责人: NANCY C WALWORTH
• 金额: $ 43.44万
• 依托单位: UNIV OF MED/DENT NJ-R W JOHNSON MED SCH
• 依托单位国家: 美国
• 财政年份: 1995
• 资助国家: 美国
• 起止时间: 1995-08-01 至 2008-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6828679
• 关键词: DNA damage; Schizosaccharomyces pombe; alleles; binding sites; biological signal transduction; cell cycle; cell cycle proteins; cell growth regulation; cytogenetics; enzyme activity; fungal genetics; fungal proteins; gene mutation; mutant; phenotype; phosphorylation; posttranslational modifications; protein kinase; protein protein interaction; protein structure function; protein transport; site directed mutagenesis; tissue /cell culture

DESCRIPTION (provided by applicant): Cell cycle checkpoints ensure the integrity of the genome from one replicative cell cycle to the next. In the event of catastrophic damage to the genome, cells of multicellular eukaryotes can undergo apoptosis, presumably to eliminate them from the cell population and reduce the risk of propagating genetically unstable cells. Alternatively, cells may respond to DNA damage by undergoing a transient arrest of the cell cycle, which correlates with their ability to survive exposure to DNA damaging agents. This response requires the DNA damage checkpoint pathway; if compromised by mutation or drug treatment, cells will enter mitosis with damaged DNA and die. The fission yeast has been an extremely valuable system for identifying and characterizing components of the DNA damage checkpoint. Indeed, many proteins that are now known to function in the checkpoint pathway in mammalian cells were identified solely based on their sequence homology to proteins that were identified genetically and functionally in yeast. Thus, it is clear that the identification of proteins in yeast using the power of classical genetics is a valid and productive means of identifying and gaining insight into the function of mammalian counterparts. Experiments described in this proposal will continue to investigate the protein kinase, Chk1, a key regulator of the checkpoint in eukaryotic cells. In addition, we will focus on a novel fission yeast protein, Msc1. Msc1 shares structural domain homology with mammalian RbBP2, a protein identified by virtue of its ability to bind the tumor suppressor protein Rb and with PLU-1, the product of a gene that is up regulated in breast cancer cells. Msc1 was cloned because it can compensate for the loss of function Chk1. The Msc1 protein appears to be important or histone modifications of chromatin, for genomic stability and for survival after DNA damage. Experiments described in this proposal aim to dissect the role of the Msc1 protein in fission yeast, to lay the groundwork for understanding the functions of the human homologues.

描述（由申请方提供）：细胞周期检查点确保基因组从一个复制细胞周期到下一个复制细胞周期的完整性。在基因组发生灾难性损伤的情况下，多细胞真核生物的细胞可以经历凋亡，大概是为了将它们从细胞群中消除并降低繁殖遗传不稳定细胞的风险。或者，细胞可以通过经历细胞周期的短暂停滞来响应DNA损伤，这与它们暴露于DNA损伤剂而存活的能力相关。这种反应需要DNA损伤检查点途径;如果受到突变或药物治疗的影响，细胞将进入DNA受损的有丝分裂并死亡。裂殖酵母是一个非常有价值的系统，用于鉴定和表征DNA损伤检查点的组分。事实上，现在已知在哺乳动物细胞中的检查点途径中起作用的许多蛋白质仅基于它们与在酵母中遗传和功能上鉴定的蛋白质的序列同源性来鉴定。因此，很明显，利用经典遗传学的力量识别酵母中的蛋白质是识别和深入了解哺乳动物对应物功能的有效且富有成效的手段。本提案中描述的实验将继续研究蛋白激酶Chk 1，这是真核细胞中检查点的关键调节因子。此外，我们将重点关注一种新的裂变酵母蛋白，Msc 1。MSC 1与哺乳动物RbBP 2（一种通过结合肿瘤抑制蛋白Rb的能力而鉴定的蛋白质）和PLU-1（乳腺癌细胞中上调的基因产物）具有结构域同源性。克隆MSC 1是因为它可以补偿Chk 1功能的丧失。Msc 1蛋白似乎是重要的染色质的组蛋白修饰，基因组的稳定性和DNA损伤后的生存。本提案中描述的实验旨在剖析Msc 1蛋白在裂殖酵母中的作用，为理解人类同源物的功能奠定基础。