grant

Investigating the in vivo regulation of Dynein activity

Organization AUGUSTA UNIVERSITYLocation AUGUSTA, UNITED STATESPosted 1 May 2025Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY2026AddressAmyotrophic Lateral SclerosisAmyotrophic Lateral Sclerosis Motor Neuron DiseaseAran-Duchenne diseaseBindingBiotinBody TissuesCell BodyCell ComponentsCell FunctionCell PhysiologyCell PolarityCell ProcessCell StructureCell divisionCellsCellular FunctionCellular PhysiologyCellular ProcessCellular StructuresClosure by LigationCommunicationCompensationComplexCoupledCruveilhier diseaseCytoplasmDNA mutationDefectDegenerative Neurologic DisordersDrosophilaDrosophila genusDrosophila melanogasterDyneinDynein ATPaseDynein Adenosine TriphosphataseDynein AdenosinetriphosphataseEmbryoEmbryonicEukaryotic CellFamilyFemaleFliesGehrig's DiseaseGenetic ChangeGenetic defectGenetic mutationGerm LinesGoalsHumanIn VitroKinesinKnowledgeLigaseLigase GeneLigationLinkLocomotor ActivityLou Gehrig DiseaseLower ExtremityLower LimbMaintenanceMammaliaMammalsMediatingMembrum inferiusMessenger RNAMicro-tubuleMicrotubulesMinus End of the MicrotubuleModelingModern ManMolecularMolecular InteractionMolecular MotorsMorphogenesisMotilityMotorMotor ActivityMutationNamesNervous System Degenerative DiseasesNervous System DiseasesNervous System DisorderNeural Degenerative DiseasesNeural degenerative DisordersNeurodegenerative DiseasesNeurodegenerative DisordersNeurologic Degenerative ConditionsNeurologic DisordersNeurological DisordersNon-Polyadenylated RNANongrowing End of the MicrotubuleOocytesOrganellesOvocytesParalysis AgitansParkinsonParkinson DiseasePhenotypePost-Transcriptional Gene SilencingPrimary ParkinsonismProcessProteinsPublishingRNARNA Gene ProductsRNA InterferenceRNA SilencingRNAiRegulationRibonucleic AcidSequence-Specific Posttranscriptional Gene SilencingSpecificitySpinal Muscular AtrophySubcellular ProcessSynthetasesSystemTestingTissuesVesicleVitamin Hanterograde transportcellular polaritycoenzyme Rdegenerative diseases of motor and sensory neuronsdegenerative neurological diseasesdynactindynein activator proteineggexperimentexperimental researchexperimental studyexperimentsflyfruit flygenome mutationhuman diseasein vivoinsightloss of function mutationmRNAmorphogenetic processnamenamednamingnerve cell deathnerve cell lossneurodegenerative illnessneurological diseaseneuron cell deathneuron cell lossneuron deathneuron lossneuronal cell deathneuronal cell lossneuronal deathneuronal lossnineinnovelreproductiveretrograde transportsingle molecule
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Full Description

The establishment and maintenance of polarity is a fundamental feature of eukaryotic cells. Molecular motors
within cells transport a variety of cargo including RNAs, proteins, vesicles, and organelles. The asymmetric

distribution of these cargos by motor proteins is the underlying basis of cell polarity. The focus of this

application is on the microtubule motor, cytoplasmic Dynein. Dynein is responsible for the transport of most

cellular cargo towards the microtubule minus-end. In the absence of cargo, Dynein has limited activity. Fully

activating this motor requires the multi-subunit Dynactin complex, and one of several activating cargo adaptors.

As suggested by their name, cargo adaptors link Dynein with cargo and are also required for stimulating the

activity of the motor. The majority of studies regarding the mechanism of Dynein activation have been

performed using in vitro single molecule experiments. By contrast, much less is known regarding how this

motor is activated in vivo and which cargo adaptors are critical for its activity. Addressing this gap is knowledge

is the focus of this application. The model that I propose to use for these studies is the well-characterized

Drosophila melanogaster egg chamber, the reproductive tissue of the female fly. Dynein is essential for the

proper maturation of the Drosophila egg chamber and oocyte, and numerous cargoes are known to be

transported by Dynein in this tissue. Thus, the egg chamber is an ideal model for examining the mechanism of

cargo adaptor mediated Dynein activation. Based on my preliminary results, I will test two hypotheses. In Aim

1, I will test the hypothesis that Bicaudal-D (BicD) is the primary activation cargo adaptor for Dynein in the

female germline. In Aim 2, I will test the hypothesis that in the absence of the cargo adaptors Hook or Ninein,

that BicD is able to functionally compensate for their loss.

Grant Number: 5F31GM157952-02
NIH Institute/Center: NIH

Principal Investigator: Phylicia Allen

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