grant

Functional Analysis of microRNAs in C. elegans spermatogenesis

Organization MARQUETTE UNIVERSITYLocation MILWAUKEE, UNITED STATESPosted 21 Sept 2017Deadline 31 Aug 2026
NIHUS FederalResearch GrantFY20223' Untranslated Regions3'UTRAddressAnimalsAntigenic DeterminantsBinding DeterminantsBinding SitesBiochemicalBiologic ModelsBiological ModelsC elegansC elegans genomeC. elegansC. elegans genomeC.elegansC.elegans genomeC2H2 Zinc FingerCRISPR approachCRISPR based approachCRISPR methodCRISPR methodologyCRISPR techniqueCRISPR technologyCRISPR toolsCRISPR-CAS-9CRISPR-based methodCRISPR-based techniqueCRISPR-based technologyCRISPR-based toolCRISPR/CAS approachCRISPR/Cas methodCRISPR/Cas technologyCRISPR/Cas9CRISPR/Cas9 technologyCaenorhabditis elegansCaenorhabditis elegans genomeCancersCardiovascular DiseasesCas nuclease technologyCell BodyCellsChimeraChimera organismClustered Regularly Interspaced Short Palindromic Repeats approachClustered Regularly Interspaced Short Palindromic Repeats methodClustered Regularly Interspaced Short Palindromic Repeats methodologyClustered Regularly Interspaced Short Palindromic Repeats techniqueClustered Regularly Interspaced Short Palindromic Repeats technologyCombining SiteDataData AnalysesData AnalysisData SetDatasetDefectDegenerative Neurologic DiseasesDegenerative Neurologic DisordersDevelopmentEducationEducational aspectsEpitopesFamilyFluorescence Light MicroscopyFluorescence MicroscopyFoundationsFutureGTP PhosphohydrolasesGTPasesGametesGene Action RegulationGene ExpressionGene Expression RegulationGene RegulationGene Regulation ProcessGenesGeneticGenetic AlterationGenetic ChangeGenetic defectGerm CellsGerm LinesGerm-Line CellsGoalsGonadal structureGrantGuanosine Triphosphate PhosphohydrolasesGuanosinetriphosphatasesHermaphroditismImmune PrecipitationImmunoprecipitationIndividualInjectionsIntersexualityInvestigationKnowledgeMalignant NeoplasmsMalignant TumorMessenger RNAMicro RNAMicroRNAsModel SystemMolecularMolecular GeneticsMutationNervous System Degenerative DiseasesNeural Degenerative DiseasesNeural degenerative DisordersNeurodegenerative DiseasesNeurodegenerative DisordersNeurologic Degenerative ConditionsNon-Polyadenylated RNAOralOrganismPathway interactionsPhysiologyPlayPopulationPostdocPostdoctoral FellowProcessProductionProteinsPublicationsR-Series Research ProjectsR01 MechanismR01 ProgramRNARNA Gene ProductsReactive SiteRegulationRegulator GenesReproductive CellsResearchResearch AssociateResearch GrantsResearch Project GrantsResearch ProjectsRibonucleic AcidRoleScientific PublicationScientistSex CellSite-Directed MutagenesisSite-Specific MutagenesisSmall RNASpermSpermatogenesisSpermatozoaStudentsSystemTargeted DNA ModificationTargeted ModificationTechniquesTestingTrainingTranscriptional Regulatory ElementsWorkcardiovascular disordercross-linkcrosslinkdata interpretationdegenerative diseases of motor and sensory neuronsdegenerative neurological diseasesdesigndesigningdevelopmentalexperimentexperimental researchexperimental studygenetic approachgenetic strategygenome mutationgonadgonadsgraduate studentguanosinetriphosphatasehuman diseaseinitial cellinterestliving systemmRNAmalemalignancymeetingsmiRNAmiRNAsmultiple data setsmultiple datasetsmutantneoplasm/cancerneurodegenerative illnesspathwaypost-docpost-doctoralregulatory genesexual cellsocial rolesperm cellsuccesstrans acting elementundergradundergraduateundergraduate researchundergraduate research experienceundergraduate research opportunitiesundergraduate research programsundergraduate studentzoosperm
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Full Description

7. PROJECT SUMMARY
Small RNAs, including microRNAs, have been shown to play critical roles in the regulation of

gene expression in the germ line. However, the specific pathways and targets regulated by individual

microRNAs in the process of spermatogenesis remain largely unknown. The identification of direct

targets regulated by individual microRNAs remains a central challenge in the field. In this grant, we

propose to identify direct targets of germline microRNAs that function in the regulation of

spermatogenesis. We are using the model system of C. elegans, which has been instrumental in defining

the core principles of individual microRNA regulation of targets in developmental pathways. In prior

work, we and others have identified the set of microRNAs that are expressed in C. elegans germ cells and

somatic gonad cells. Additionally, we have identified a set of microRNAs that function to regulate sperm

formation. However, the pathways and targets that they regulate remain largely uncharacterized. This

work will address two central questions: 1) What are the target mRNAs that associate with a germline

specific Argonaute protein? 2) How does regulation by microRNAs through the 3’ UTR of target mRNAs

act to control spermatogenesis? This work will provide a foundation for future investigation to

comprehensively define the microRNA targets that act in the germ line to regulate the process of

spermatogenesis.

Grant Number: 2R15GM126458-02
NIH Institute/Center: NIH

Principal Investigator: Allison Abbott

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