Pathophysiology of MECP2 Spectrum Disorders (Career Development Award Proposal)
Pathophysiology of MECP2 Spectrum Disorders (Career Development Award Proposal)
批准号:
8098741
负责人:
MELISSA Beth RAMOCKI
金额:
$17.04万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-08-15 至 2013-07-31
关键词:
Advisory CommitteesAffectAnimalsAntibodiesAnxietyAttentionAutistic DisorderBiological ModelsBipolar DisorderBlindedBreathingCandidate Disease GeneCell LineCharacteristicsChildChromatinChromatin StructureComplementDevelopmentDiagnosticDiseaseEncephalopathiesEnvironmentEpigenetic ProcessEpilepsyFamilyFemaleFunctional disorderFutureGene ActivationGene DuplicationGene MutationGene TargetingGenesGenomeGoalsHandHistone DeacetylaseHistone H3HistonesHumanHypothalamic structureK-Series Research Career ProgramsLabelLearningLearning DisabilitiesLinkLysineMaintenanceMedicineMental RetardationMentorsMethyl-CpG-Binding Protein 2MethylationMicrocephalyMissense MutationModelingModificationMolecularMotorMotor ActivityMovement DisordersMusMutationNeurodevelopmental DisorderNeurologicNeurologic DysfunctionsNeuronsPathologyPatientsPatternPhenotypePhysiciansPsychotic DisordersRNA SplicingRegulationResearchResearch PersonnelRett SyndromeRoleSamplingSchizophreniaScientistSecondary toSeizuresSocial InteractionSodium ButyrateSpeechSymptomsSyndromeTechnologyTestingTherapeuticTissuesTrainingTremorVariantWeightautism spectrum disorderbasecareerchromatin immunoprecipitationchromatin modificationcohortcollegedesigndisease phenotypedosageearly onsetgain of functiongene repressionhistone modificationhuman maleimprovedinfancyloss of functionlymphoblastmalemouse modelnervous system disorderpostnatalprognosticprogramspromoterresearch studyresponserestorationskillsstereotypysuccesstranscription factor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): MECP2 spectrum disorders include classic Rett syndrome, females with Rett syndrome variants, Angelman-like phenotypes, autism, mental retardation, learning disabilities, attention disorders, as well as males with Rett syndrome, fatal infantile encephalopathy, mental retardation with tremors/movement disorders and/or seizures, or early onset psychosis in the form of bipolar disorder or schizophrenia. The mechanism by which alterations in the MeCP2 protein itself, or the dosage of MeCP2 protein, result in the various disease phenotypes is unclear. My proposal seeks to understand these mechanisms so that rational treatments can be developed to help children with MECP2 spectrum disorders.
My goal is to determine how loss of function and missense mutations, as well as duplication of MECP2, cause neurological dysfunction. The specific aims of my proposal are 1) to identify global patterns of chromatin modification and 2) to identify specific MECP2 target genes in human and mouse models of MECP2 spectrum disorders and 3) to test the hypothesis that therapy targeted to epigenetic modifications improves symptoms in mouse models of MECP2 dysfunction. I propose to use ChlP-on-chip technology to test the hypothesis that loss of function and missense mutations, as well as duplication of MECP2, cause neurological dysfunction by altering chromatin states at specific loci resulting in the misregulated expression of select genes, and that restoration of the normal chromatin state will improve symptoms associated with a subset of MECP2 alterations.
My long term goal is to become an independent physician scientist with a research program designed to investigate the molecular basis of autistic spectrum disorders, mental retardation, and developmental epilepsy syndromes and ultimately help clinicians provide accurate diagnostic, prognostic, and therapeutic information to patients and their families. Baylor College of Medicine provides the perfect environment for my success. My mentor, Dr. Huda Zoghbi, is an internationally known physician/scientist with a tremendous training record. Departmental support of my research career, interaction with a scientific advisory committee, and formal coursework at Baylor and elsewhere will also help me to achieve my goals.
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Pathophysiology of MECP2 Spectrum Disorders (Career Development Award Proposal)
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批准号:8303314
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项目类别:
-
资助金额:$18.0万
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财政年份:2008
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负责人:MELISSA Beth RAMOCKI
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依托单位:
Pathophysiology of MECP2 Spectrum Disorders (Career Development Award Proposal)
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批准号:7675939
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项目类别:
-
资助金额:$17.04万
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财政年份:2008
-
负责人:MELISSA Beth RAMOCKI
-
依托单位:
Pathophysiology of MECP2 Spectrum Disorders (Career Development Award Proposal)
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批准号:7894528
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项目类别:
-
资助金额:$17.04万
-
财政年份:2008
-
负责人:MELISSA Beth RAMOCKI
-
依托单位:
Pathophysiology of MECP2 Spectrum Disorders (Career Development Award Proposal)
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批准号:7509198
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项目类别:
-
资助金额:$17.04万
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财政年份:2008
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负责人:MELISSA Beth RAMOCKI
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依托单位:
海外基金