The regulation of synaptic specificity in the mammalian retina
The regulation of synaptic specificity in the mammalian retina
批准号:
10436960
负责人:
Elizabeth Zuniga-Sanchez
金额:
$23.79万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-07-01 至 2023-06-30
关键词:
AddressAdvisory CommitteesApplications GrantsBindingBinding ProteinsBiological AssayCRISPR/Cas technologyCell Adhesion MoleculesCell Surface ProteinsCell surfaceCellsClustered Regularly Interspaced Short Palindromic RepeatsCollaborationsComplexConeDataData SetDefectDevelopmentEducational workshopElectroporationFacultyGene ExpressionGenesGoalsHealthHumanInstitutionKnock-outMediatingMentorsMentorshipMissionMolecularMusNRCAM geneNational Eye InstituteNeural RetinaNeuraxisNeuronsPathway interactionsPhasePhenotypePhotoreceptorsPositioning AttributePreparationProcessProteinsPublic HealthRegulationResearchResearch PersonnelResourcesRestRetinaRetinal ConeRetinal DiseasesRodRoleScheduleSignal TransductionSpecific qualifier valueSpecificitySynapsesSystemTestingTherapeuticTissue-Specific Gene ExpressionTrainingTranscriptVertebrate PhotoreceptorsVisionVisual system structureWNT Signaling PathwayWorkbasecareercareer developmentcell typedesigndifferential expressionexperimental studygain of functiongene functiongenetic manipulationin vivoinsightmeetingsneurodevelopmentnovelpostsynapticpresynapticprofessorretinal rodsscreeningsegregationsight restorationsynaptogenesistenure tracktranscriptometranscriptome sequencingvision development
中文摘要
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英文摘要
Abstract
Establishing proper retinal circuitry remains a central issue in visual system development. How neurons find
their correct target remains largely unknown. The first synapse in the retina provides a simple and
experimentally tractable system to explore the basis of synaptic specificity. Rod and cone photoreceptors
synapse selectively with rod bipolars and cone bipolars, respectively. To identify the molecular mechanism
mediating specificity, I generated transcriptome profiles of the different photoreceptors and their corresponding
bipolar cell targets during synaptogenesis. From these data sets, I find distinct transcripts encoding cell surface
and secreted proteins as promising candidates for this process. Using in vivo genetic manipulations and
developmental approaches, I will assess the function of these genes in establishing proper connectivity. From
my initial screen, I find the following: 1) non-canonical Wnt signaling between rods and rod bipolars is
responsible for dictating the position of the synaptic layer, 2) Rspo2 in rods is involved in layer segregation,
and 3) Nrcam in cones mediates selective connectivity to cone bipolars. I subdivided this proposal into two
parts where I study rod-to-rod bipolar connectivity in Aim 1 and address cone-to-cone bipolar connectivity in
Aim 2. The first section of each aim involves expanding on my preliminary findings and will be completed in the
K99 phase. The second part involves continue screening and expanding on the new phenotypes which will be
initiated under the mentorship of Dr. S. Lawrence Zipursky and will be completed during the R00 phase.
This project has been designed to facilitate Dr. Zuniga-Sanchez to obtain a position as a tenure-track Assistant
Professor at a top-tier academic research institution. With the help of her mentor and Advisory Committee, she
has generated promising data and made significant progress on her research. As an independent investigator,
she plans to continue her work studying the development of the mammalian retina with a clear relevance to
human health. During the K99 phase, she will continue benefiting from the mentorship on the developing visual
system from Dr. Zipursky. She will also receive additional career and scientific guidance at regular scheduled
meeting and presentations with her Advisory Committee. Dr. Zuniga-Sanchez will participate in career
development workshops offered through UCLA in preparation to apply for faculty positions and transitioning to
the R00 phase. This grant proposal outlines the training, resources, and network of collaborations needed to
establish Dr. Zuniga-Sanchez as an independent investigator in the vision field.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1016/j.neuron.2018.03.004
发表时间:
2018-04-04
期刊:
Neuron
影响因子:
16.2
作者:
[Sarin S, Zuniga-Sanchez E, Kurmangaliyev YZ, Cousins H, Patel M, Hernandez J, Zhang KX, Samuel MA, Morey M, Sanes JR, Zipursky SL]
通讯作者:
Zipursky SL
Deciphering the molecular mechanisms in photoreceptor wiring
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批准号:10617929
-
项目类别:
-
资助金额:$7.22万
-
财政年份:2021
-
负责人:Elizabeth Zuniga-Sanchez
-
依托单位:
Deciphering the molecular mechanisms in photoreceptor wiring
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批准号:10723128
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项目类别:
-
资助金额:$7.22万
-
财政年份:2021
-
负责人:Elizabeth Zuniga-Sanchez
-
依托单位:
Deciphering the molecular mechanisms in photoreceptor wiring
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批准号:10489851
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项目类别:
-
资助金额:$38.8万
-
财政年份:2021
-
负责人:Elizabeth Zuniga-Sanchez
-
依托单位:
Deciphering the molecular mechanisms in photoreceptor wiring
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批准号:10280111
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项目类别:
-
资助金额:$40.0万
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财政年份:2021
-
负责人:Elizabeth Zuniga-Sanchez
-
依托单位:
Deciphering the molecular mechanisms in photoreceptor wiring
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批准号:10654028
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项目类别:
-
资助金额:$40.0万
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财政年份:2021
-
负责人:Elizabeth Zuniga-Sanchez
-
依托单位:
The regulation of synaptic specificity in the mammalian retina
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批准号:10179396
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项目类别:
-
资助金额:$23.62万
-
财政年份:2020
-
负责人:Elizabeth Zuniga-Sanchez
-
依托单位:
The regulation of synaptic specificity in the mammalian retina
-
批准号:9370779
-
项目类别:
-
资助金额:$10.75万
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财政年份:2017
-
负责人:Elizabeth Zuniga-Sanchez
-
依托单位:
Jagged-Notch and Fgf signaling: patterning the vertebrate upper face
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批准号:7936846
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项目类别:
-
资助金额:$3.05万
-
财政年份:2009
-
负责人:Elizabeth Zuniga-Sanchez
-
依托单位:
Jagged-Notch and Fgf signaling: patterning the vertebrate upper face
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批准号:8288026
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项目类别:
-
资助金额:$0.26万
-
财政年份:2009
-
负责人:Elizabeth Zuniga-Sanchez
-
依托单位:
Jagged-Notch and Fgf signaling: patterning the vertebrate upper face
-
批准号:8123362
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项目类别:
-
资助金额:$3.1万
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财政年份:2009
-
负责人:Elizabeth Zuniga-Sanchez
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依托单位:
海外基金