Identification of the genetic pathways that give rise to the chicken rod-free zone and human fovea using epigenomic profiling
Identification of the genetic pathways that give rise to the chicken rod-free zone and human fovea using epigenomic profiling
批准号:
9899991
负责人:
Brian P Hafler
金额:
$27.71万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-01 至 2021-06-30
关键词:
ATAC-seqAgeAge related macular degenerationAnatomyAreaBindingBinding SitesBiological AssayBiological ModelsCRISPR/Cas technologyCandidate Disease GeneCellsChickensChromatinClinicalConeConserved SequenceDataDevelopmentElectrophoretic Mobility Shift AssayElectroporationEmbryoEnvironmentFutureGene ExpressionGenerationsGenesGeneticGoalsHumanHuman DevelopmentImmunohistochemistryIn Situ HybridizationInheritedInstitutesInvestigationJournalsK-Series Research Career ProgramsKnowledgeLaboratoriesLeadMacular degenerationMedicalMentorsMethodsMolecularOphthalmologyOptic vesiclePathway AnalysisPathway interactionsPatientsPatternPeripheralPhotoreceptorsPhylogenetic AnalysisProcessQuality of lifeRegulationReplacement TherapyReporterReporter GenesResearchResearch PersonnelResearch ProposalsRetinaRetinal ConeRetinal DiseasesRodScientistSiteSpottingsStructureTestingThyroid HormonesTissuesTrainingTraining ProgramsTranscriptTranscription Initiation SiteTransposaseVisionVisual AcuityWorkbasecandidate identificationcareercareer developmentdesignepigenomicsexperiencefovea centralisimprovedin vivoinsightinterestmacular dystrophymedical schoolsnew technologyprofessorprogramspublic health relevanceretinal progenitor cellretinal rodsskillstranscription factortranscriptometranscriptome sequencing
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): This mentored clinical scientist research career development award is a training program designed to help the candidate achieve his long-term career goal to have an academic career with a focus on the retina. For the current training and future career, Brian Hafler intends to perform research focused on understanding the molecular mechanisms underlying development of the human fovea and translational applications to retinal disease. The fovea is responsible for high acuity central vision, yet the genes that establish this region are unknown. This research proposal will focus on identifying the molecular pathways that generate this region using the chicken as a model system, as it has a central rod-free spot, much like the human fovea. In this research proposal, Dr. Hafler will use new technologies like ATAC-seq to perform open chromatin profiling of cells in the developing chicken rod-free zone. ATAC-seq data will be compared with RNA-seq data, which is in the process of being generated in the Cepko lab to prioritize candidate genes of interest. Immunohistochemistry and in situ hybridization will be performed to assess whether the transcripts associated with regions of open chromatin specifically localize to the rod-free central
zone in the chicken embryonic retina. Candidate cis- regulatory modules located in regions of open chromatin will be aligned and assessed for conservation with species that contain a fovea. The most promising sequences will be cloned into reporter constructs and tested for activity in the developing chicken retina using electroporation assays. Transcription factors that bind to the cis-regulatory modules will be identified using electrophoretic mobility shift assays. Immunohistochemistry and in situ hybridization on embryonic human retinas will be used to examine if the transcription factors of interest are conserved during human retinal development. Completion of this work would not only give insight into how the fovea is generated during human development, it will also help with the development of cell replacement therapies for patients with age-related macular degeneration. The candidate has an excellent mentor, Dr. Constance Cepko, who is a leader in the field and is committed to the scientific development and execution of the project. She is the Bullard Professor of Genetics and Ophthalmology at Harvard Medical School and a Howard Hughes Medical Institute Investigator. The environment at Harvard Medical School has a strong and established research program related to retinal development. They will provide necessary facilities for career enhancement to become an independent investigator. There are numerous courses offered, seminars, journal clubs, and presentations with opportunities for intellectual interactions with other research scientists. The experience, knowledge, and skills gained through the research plan and career development activities will carry the candidate forward towards a career as an independent clinician-scientist.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1097/iae.0000000000001341
发表时间:
2017-03
期刊:
Retina (Philadelphia, Pa.)
影响因子:
--
作者:
[Hafler BP]
通讯作者:
Hafler BP
Targeting the inflammatory response in age-related macular degeneration
-
批准号:10504138
-
项目类别:
-
资助金额:$41.88万
-
财政年份:2022
-
负责人:Brian P Hafler
-
依托单位:
Targeting the inflammatory response in age-related macular degeneration
-
批准号:10707366
-
项目类别:
-
资助金额:$41.88万
-
财政年份:2022
-
负责人:Brian P Hafler
-
依托单位:
Identification of the genetic pathways that give rise to the chicken rod-free zone and human fovea using epigenomic profiling
-
批准号:9248366
-
项目类别:
-
资助金额:$27.69万
-
财政年份:2016
-
负责人:Brian P Hafler
-
依托单位:
Regulation of Olig2 in Motor Neuron Development
-
批准号:7274801
-
项目类别:
-
资助金额:$5.01万
-
财政年份:2006
-
负责人:Brian P Hafler
-
依托单位:
Regulation of Olig2 in Motor Neuron Development
-
批准号:7156528
-
项目类别:
-
资助金额:$4.89万
-
财政年份:2006
-
负责人:Brian P Hafler
-
依托单位:
Regulation of Olig2 in Motor Neuron Development
-
批准号:7468016
-
项目类别:
-
资助金额:$2.0万
-
财政年份:2006
-
负责人:Brian P Hafler
-
依托单位:
国内基金
海外基金
登录
查看更多内容
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
-
批准号:JCZRLH202601523
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:
-
依托单位:
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
-
批准号:JCZRQN202500010
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:
-
依托单位:
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
-
批准号:2025JJ70209
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:雷芬芳
-
依托单位:
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
-
批准号:--
-
项目类别:面上项目
-
资助金额:--
-
批准年份:2024
-
负责人:万荣
-
依托单位:
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
-
批准号:2023JJ50274
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2023
-
负责人:贺志明
-
依托单位:
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
-
批准号:--
-
项目类别:地区科学基金项目
-
资助金额:33万元
-
批准年份:2022
-
负责人:都义日
-
依托单位:
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
-
批准号:--
-
项目类别:面上项目
-
资助金额:52万元
-
批准年份:2022
-
负责人:叶宝东
-
依托单位:
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2022
-
负责人:于海兵
-
依托单位:
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
-
批准号:81973577
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2019
-
负责人:辛贵忠
-
依托单位:
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
-
批准号:81602908
-
项目类别:青年科学基金项目
-
资助金额:18.0万元
-
批准年份:2016
-
负责人:刘括
-
依托单位: