Mechanisms of Wnt signaling in cell polarity and cell migration
Mechanisms of Wnt signaling in cell polarity and cell migration
批准号:
7944037
负责人:
Wayne C. Forrester
金额:
$19.24万
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:
2009-09-30 至 2012-08-31
关键词:
Abnormal CellAffectAnteriorAxonBiological AssayBone DevelopmentBrainC. elegans genomeCaenorhabditis elegansCancerousCell PolarityCellsComplexCongenital Heart DefectsCongenital MegacolonCuesDendritesDestinationsDevelopmentDiseaseEpitheliumExhibitsFZD2 geneFamilyGenesGenetic ScreeningGrantGrowth ConesHomologous GeneHumanHuman DevelopmentIndividualIntestinal DiseasesInvestigationLeadLearningLightLinkMAPK8 geneMalignant NeoplasmsMethodsModelingMolecular GeneticsMutationNervous system structureNeuronsOutcomePathway interactionsPhosphotransferasesPositioning AttributeProcessProtein Tyrosine KinaseProteinsReceptor Protein-Tyrosine KinasesRobinow syndromeRoleRor receptor tyrosine kinaseSignal PathwaySignal TransductionSpecific qualifier valueSyndromeTestingTo specifyWnt proteinsWorkcell motilitydevelopmental diseasehuman FZD2 proteinin vivoinsightinterestlissencephalymembermigrationneuronal cell bodyoverexpressionreceptorresearch studystress-activated protein kinase 1
中文摘要
适当控制细胞迁移对后生动物的发育至关重要。定向迁移需要保密
英文摘要
The proper control of cell migration is critical for metazoan development. Directed migration requires secreted
extracellular signals that act through cell surface receptors to guide the migrations of those cells. Secreted Wnt
proteins are members of a major class of extracellular signals that orient cell and tissue polarity, specify cell
fates, and direct cell migrations of numerous cell types. Mutation of Wnt signaling cascade genes are
associated with the development of human cancers; thus understanding how Wnt proteins act is of significant
biomedical importance. C. elegans neuronal cell migration serves as an excellent model for understanding how
signaling pathways modulate cell polarity and migration due to the fascile genetic manipulation of this organism
and the ability to visualize directly the migrating cells. We previously identified mutations in the CAM-1 gene,
which encodes a Ror type receptor tyrosine kinase (RTK) required for directing migrating cells to their proper
destination. We found that CAM-1 acts, apparently as a traditional RTK, to orient neuronal polarity. We
propose experiments to decipher its mechanism of action in orienting neuronal polarity. In addition, we have
identified 41 new mutations that affect cell migration, including the first mutation in cfz-2, a C. elegans Frizzled
receptor, which is involved in Wnt signaling. We propose to use large-scale DNA sequencing to rapidly clone at
least three of our new migration genes from this screen. The identification and mechanistic understanding of
the roles of these new genes will provide new insight into the processes that control cell migration.
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