Chromatin remodeling at cell cycle exit
Chromatin remodeling at cell cycle exit
批准号:
9979649
负责人:
Laura A Buttitta
金额:
$31.85万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-08-01 至 2023-07-31
关键词:
Activity CyclesAddressBindingBiologicalBiological MetamorphosisBypassCell CycleCell Cycle ArrestCell Cycle RegulationCell Differentiation processCell MaintenanceCell ProliferationCellsChromatinCoupledDataDevelopmentDevelopmental ProcessDrosophila eyeDrosophila genusDrosophila melanogasterElementsEnhancersEpithelialEpitheliumEventFAIRE sequencingG0 PhaseGene ExpressionGenesGeneticGenetic ScreeningGenomeGoalsMaintenanceMalignant NeoplasmsMediatingModelingMolecularNucleosomesPatternProcessProliferatingPupaRegulator GenesRegulatory ElementResearchRoleShapesSignal PathwaySignal TransductionTestingTimeTissue DifferentiationTissuesTrans-ActivatorsWingWithdrawalWorkcdc Genescell fate specificationcell typechromatin remodelingflexibilityflygenetic manipulationin vivomature animaltissue regenerationtooltranscription factortranscriptometranscriptome sequencing
中文摘要
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英文摘要
Project Summary/Abstract
Cell proliferation must be precisely controlled during development to produce tissues of the correct shape,
composition and size. Terminal differentiation is often associated with exit from the cell cycle and coupled with
a switch to a permanently postmitotic state. This is an important developmental process, as permanent exit
from the cell cycle is likely to represent the most common cellular state in adult animals. Our data indicates a
critical role for specific nucleosome remodelers in proper initiation and maintenance of cell cycle exit. This is
consistent with our finding that accessibility at many gene regulatory elements also changes during cell cycle
exit. The goal of our proposed research is to understand how cell cycle gene expression is shut down
at the right places and times during development to establish and maintain a stable postmitotic state in
differentiating tissues. To accomplish this, we propose three aims: 1. To define the specific gene expression
and regulatory element accessibility changes that are due to cell cycle exit and how they are altered upon
forced cell cycle re-entry 2. To determine how developmental signals coordinate cell cycle exit with
differentiation events and 3. To understand the role of specific nucleosome remodelers in promoting cell cycle
exit.
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资助金额:$34.35万
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依托单位:
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负责人:Laura A Buttitta
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依托单位:
海外基金