Patterning the cell: role of the PAR-1 kinase
Patterning the cell: role of the PAR-1 kinase
批准号:
9273897
负责人:
Andrew William Folkmann
金额:
$5.92万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-05-15 至 2018-05-14
关键词:
AnteriorArchitectureBiochemicalBiochemistryCaenorhabditis elegansCell Differentiation processCell PolarityCell divisionCellsCellular biologyClustered Regularly Interspaced Short Palindromic RepeatsCytoplasmDevelopmentDiseaseDissectionEmbryoFertilizationGenetic ScreeningHealthHumanLeadLocationMediatingMolecularMutationOrthologous GenePathologyPatternPhenotypePhosphotransferasesProcessProtein-Serine-Threonine KinasesProteinsRNA InterferenceRegulationRoleSignal TransductionSignaling MoleculeStereotypingStructureTechniquesTechnologyTestingTimeTissuesWorkYeastscell typechemical geneticsdaughter cellegggenetic analysisgenome editinghuman diseasein vivonew technologynoveloptogeneticspublic health relevancezygote
中文摘要
英文摘要
DESCRIPTION (provided by applicant): Many cell types must become polarized to function properly within a tissue or to generate distinct daughter cells. A quintessential example of this phenomenon is observed in the eggs of Caenorhabditis elegans. Shortly after fertilization, the C. elegans zygote undergoes a dramatic, stereotyped polarization that segregates polarity factors and cell fate determinants to the anterior and posterior ends of the egg. These asymmetries are essential for cellular differentiation and organismal development. Genetic analyses have demonstrated an essential role for the conserved Serine/Threonine kinase PAR-1 in this process. Specifically, loss of par-1 protein activity in the zygote results in symmetric distributin of normally asymmetric factors. In this proposal I will combine new technologies with classical techniques to analyze PAR-1 function in live embryos. In Aim1, I will use optogenetic and Cas9 genome editing technologies to assign function to the different PAR-1 domains and test the role of PAR-1 asymmetry in patterning the zygote. In Aim 2, I will conduct an unbiased chemical genetic screen to identify critical PAR-1 substrates. This work will uncover the molecular mechanisms used by PAR-1 to pattern the zygote and regulate cell and organismal polarity.
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会议论文
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批准号:8061325
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项目类别:
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资助金额:$2.64万
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财政年份:2011
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负责人:Andrew William Folkmann
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依托单位:
Defining the role for Gle1 in the fetal lethal motor neuron disease LCCS1
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批准号:8411599
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项目类别:
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资助金额:$2.69万
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财政年份:2011
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依托单位:
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批准号:8261951
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项目类别:
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资助金额:$2.69万
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财政年份:2011
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负责人:Andrew William Folkmann
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依托单位:
海外基金