Studies of the Smc5/Smc6 complex in chromosomal replication
Studies of the Smc5/Smc6 complex in chromosomal replication
批准号:
7903094
负责人:
Xiaolan Zhao
金额:
$29.95万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-09-20 至 2012-08-31
关键词:
ATP phosphohydrolaseAddressAffectBehaviorBiochemicalBiologicalCell Cycle ArrestCellsCharacteristicsChromatidsChromatinChromosome StructuresChromosome abnormalityChromosomesComplexCruciform DNADNA StructureDNA biosynthesisDataDefectDouble Strand Break RepairEventExcisionExhibitsFaceFailureFamilyGeneticGenetic RecombinationGenomic InstabilityGoalsGrantHumanLaboratoriesLeadLesionLigaseLiteratureMaintenanceMalignant NeoplasmsMeasuresMediatingMethodsMolecularMutationNatureNuclearPathway interactionsPlayPostdoctoral FellowProcessProtein DynamicsProteinsRecoveryResearchRoleSaccharomycetalesSingle Strand Break RepairSister ChromatidStructureUbiquitinWorkcohesincohesioncondensincopinghuman diseaseinsightmembermolecular dynamicsmutantprogramsprotein complexprotein functionrecombinational repairrepairedsegregation
中文摘要
描述(申请人提供):在癌症和其他人类疾病中出现的许多染色体异常和遗传不稳定是由染色体复制缺陷引起的。染色体复制不仅需要基本复制机制的适当功能,还需要有能力应对染色质的复杂性质和模板上的损伤,这两者都可能导致复制叉子停滞或崩溃。已证明,检查点通路在促进复制恢复和完成的多项措施中发挥关键作用。此外,能够协调染色体行为和基本DNA复制程序的特殊机制也是至关重要的。SMC蛋白及其复合体,包括新鉴定的Smc5/6复合体,是一种动态的分子连接物,可以主动地连接和折叠染色单体,从而在染色体结构和复制程序之间提供重要的联系。我们的长期目标是了解染色体复制中使用的特殊程序。在这一授权期内,我们将重点介绍Smc5/6复合体在复制中的功能。我们发现Smc5/6复合体在染色体复制中发挥多种作用,其中一些作用是由其相扑E3亚基Mms21介导的。我们将结合遗传学、细胞生物学和生物化学的方法,研究Smc5/6复合体调节染色体复制的机制。在特定的目标一,我们将确定Smc5/6复合体如何在受损的复制叉处中和重组事件。在特定的目标二,我们将研究Smc5/6复合体在复制中的额外功能,并探索Smc5/6复合体与复制重要蛋白质之间的物理相互作用。这两个目标的结合结果将为复制、染色体动力学和重组修复之间的关系提供新的见解。这可能有助于理解人类Smc5/6复合体的功能,并可能导致与癌症和其他人类疾病相关的基因组不稳定的方法。染色体复制面临着染色质和核组织的复杂性带来的许多挑战。因此,它需要特殊的机制来协调染色体行为和基本的DNA复制和修复程序。进化上保守的Smc5/6复合体在这些过程的界面上发挥作用。我们描述了研究计划,以解决该复合体在染色体复制过程中共同调节不同途径的机制。这些研究的结果将为这些基本过程提供新的见解,并将有助于揭示与这些过程中的缺陷有关的人类疾病的原因和治疗方法。
英文摘要
DESCRIPTION (provided by applicant): Many chromosomal abnormalities and genetic instability arising in cancer and other human diseases are caused by defects in chromosomal replication. Chromosomal replication not only requires the proper function of the basic replication machinery, but also demands an ability to cope with the complex nature of chromatin and lesions on the template, both of which can lead to replication fork stalling or collapse. Checkpoint pathways have been shown to play key roles in mediating multiple measures that promote the recovery and completion of replication. In addition, special mechanisms that can coordinate chromosomal behavior and basic DNA replication programs are critical. SMC (structural maintenance of chromosome) proteins and their complexes, including the newly characterized Smc5/6 complex, are dynamic molecular linkers that can actively tether and fold chromatids, thereby providing important connections between chromosomal structures and replication programs. Our long-term goal is to understand the special programs utilized in chromosomal replication. In this grant period, we will focus on functions of the Smc5/6 complex in replication. We showed that the Smc5/6 complex plays multiple roles in chromosomal replication and some of its roles are mediated by its SUMO E3 subunit Mms21. Using a combination of genetic, cell biological, and biochemical approaches, we will study the mechanisms by which the Smc5/6 complex regulates chromosomal replication. In specific aim one, we will determine how the Smc5/6 complex counteracts recombinogenic events at damaged replication forks. In specific aim two, we will study the additional functions of the Smc5/6 complex in replication and probe for physical interactions between the Smc5/6 complex and proteins important for replication. The combined results from these two aims will provide new insights into the relationship between replication, chromosomal dynamics and recombinational repair. It will likely contribute to the understanding of the functions of the human Smc5/6 complex and potentially lead to methods to battle genomic instability associated with cancer and other human diseases. Chromosomal replication faces many challenges posed by the complex nature of chromatin and nuclear organization. It therefore requires special mechanisms that coordinate chromosomal behavior and basic DNA replication and repair programs. The evolutionarily conserved Smc5/6 complex functions at the interface of these processes. We describe research programs to address the mechanisms by which this complex co- regulates different pathways during chromosomal replication. Results from these studies will provide new insights into these fundamental processes and will shed lights on the cause and treatment of human diseases related to defects in these processes.
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会议论文
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海外基金