Role of CDC14B in mouse oocyte maturation
Role of CDC14B in mouse oocyte maturation
批准号:
7708686
负责人:
Karen A Schindler
金额:
$8.04万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-01 至 2011-07-31
关键词:
AneuploidyBindingCDC2 Protein KinaseCDH1 geneCell CycleCell Cycle ProgressionCellsChromosome SegregationChromosomesChromosomes, Human, Pair 1CommitConsensusCyclin-Dependent KinasesDNA biosynthesisDataDevelopmentDiploidyDiseaseDown SyndromeEmbryoEmbryonic DevelopmentEnsureEquilibriumEukaryotaEventFemaleGerm CellsGoalsGroup MeetingsHaploidyHomologous GeneHumanImaging TechniquesInfertilityLeadLearningLifeLinkMaintenanceMammalsMediatingMeiosisMeiotic M PhaseMentorsMentorshipMetaphaseMitosisMitoticMitotic Cell CycleMolecularMusOocytesOvulationPennsylvaniaPhasePhosphoric Monoester HydrolasesPhosphorylationPhosphorylation SitePostdoctoral FellowProcessProphaseProtein KinaseProteinsProteolysisRegulationReproductionResearchResearch PersonnelResearch ProposalsRestRoleScientistSignal TransductionSomatic CellSpecificitySpontaneous abortionTechnologyTestingTimeTrainingUbiquitinUniversitiesWorkanaphase-promoting complexcareeregginorganic phosphateinterestmouse modelnext generationoocyte maturationprecursor cellprematurepreventprogramssegregationsperm cellstillbirthubiquitin-protein ligaseworking groupzygote
中文摘要
描述(由申请人提供):单倍体配子是有性生殖所必需的,由二倍体前体细胞通过减数分裂产生。在女性中,卵母细胞经历2个主要的减数分裂特异性细胞周期转换,其调控机制知之甚少。第一个转变是减数分裂恢复,其中卵母细胞退出延长的前期停滞并进入第一减数分裂M期(Ml),第二个转变是Ml和MII之间的转变,其中同源染色体分离并且没有一轮DNA合成发生。这项研究提案的总体目标是确定双特异性磷酸酶CDC 14 B在小鼠卵母细胞这些转变过程中的作用,长期目标是建立一个独立的研究计划,重点是了解调节这些转变的错误如何与不孕症联系在一起。本提案的具体目的是检验以下假设:需要CDC 14 B 1)防止减数分裂过早成熟和2)通过逆转细胞周期蛋白依赖性激酶CDK 1的作用来调节MI至MII的转变。该提案的K99部分将在宾夕法尼亚大学的Richard Schultz博士的指导下进行。Schultz博士对卵母细胞成熟有着长期的兴趣,并指导了许多博士后研究员,他们现在都是成功的独立研究人员。此外,该大学致力于培养下一代科学家。本提案还描述了候选人向独立职业过渡的详细计划,包括教学课程工作和小组会议,重点是实时成像技术,候选人打算在K99阶段学习并将在R 00阶段继续使用该技术。
减数分裂是产生有性生殖所需的卵子和精子的过程。人类女性减数分裂非常容易出错;约20%的卵子含有异常染色体数量,这与自然流产、死产和发育疾病(如唐斯综合症)有关。本研究的主要目的是利用小鼠模型确定CDC 14 B磷酸酶在雌性减数分裂中的作用
英文摘要
DESCRIPTION (provided by applicant): Haploid gametes, that are essential for sexual reproduction, are generated from diploid precursor cells via meiosis. In females, oocytes undergo 2 major meiosis-specific, cell-cycle transitions whose regulation is poorly understood. The first transition is meiotic resumption where oocytes exit a prolonged prophase arrest and enter the first meiotic M phase (Ml), and the second is the transition between Ml and MIl where homologous chromosomes separate and no round of DNA synthesis occurs. The overall goal of this research proposal is to determine the role of the dual-specificity phosphatase CDC14B during these transitions in mouse oocytes with a long-term goal of establishing an independent research program that focuses on understanding how errors in regulating these transitions are linked to infertility. The specific aims of this proposal are to test the hypotheses that CDC14B is required to 1) prevent premature meiotic maturation and to 2) regulate the MI-to-MII transition through reversing the actions of the cyclin-dependent kinase, CDK1. The K99 portion of this proposal will be conducted under the mentorship of Dr. Richard Schultz at the University of Pennsylvania. Dr. Schultz has a long-standing interest in oocyte maturation and has mentored many postdoctoral fellows who are now successful independent investigators. Furthermore, the university is committed to training the next generation of scientists. This proposal also describes a detailed plan for the candidate's transition to an independent career including didactic course work and group meetings with a focus on live imaging techniques, a technology the candidate intends on learning in the K99 phase and will continue to use during the R00 phase.
PUBLIC RELEVANCE: Meiosis is the process that generates eggs and sperm required for sexual reproduction. Female meiosis is highly error-prone in humans; ~20% of all eggs contain abnormal chromosome numbers that are linked to spontaneous abortions, stillbirths and developmental diseases like Downs Syndrome. The major goal of this proposal is to determine the role for the CDC14B phosphatase during meiosis in females using the mouse model
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Control of mammalian meiosis I through protein kinase signaling
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资助金额:$35.11万
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Role of CDC14B in mouse oocyte maturation
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Role of CDC14B in mouse oocyte maturation
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