. Ankyrinproteins,ankyrin-R(ANK1),ankyrin-B(ANK2),andankyrin-G(ANK3),referredtoasAnkR, AnkB,andAnkGrespectively,arefoundthroughoutthebodyandactastheprimarylinkbetweenthespectrin- basedcytoskeletonandthecytoplasmicdomainofmanymembrane-associatedproteinsthroughtheir conserved24ANKrepeats.AlthoughAnkGandAnkBarewellrecognizedasimportantdomainorganizers withinthenervoussystem,fewstudieshaveinvestigatedAnkR?srole.Instead,researchintothefunctionof AnkRhaspredominatelyfocusedonitsfunctioninerythrocyteswhereitcreatesstructuralstabilityby anchoringBand3toIspectrin2,withmutationsinAnkRresultinginseverespherocyticanemia.Interestingly though,ourlabrecentlyshowedAnkRcancompensateforalossofAnkGandclusterNa+channelsatnodes ofRanvier,suggestinganeurologicalrole.Additionally,multiplestudieshaveindicatedvariousneurological disturbanceshavedisruptionsinAnkR,includingcerebellardysfunctionandAlzheimer?s disease.Yetstill,theexpressionprofile,consequencesofdisruption,andinteractingproteinsof AnkRinthenervoussystemremainpoorlyunderstood.Ihypothesizethattheankyrinfamilyofproteinsplay complementary,butdistinctrolesinthebrainwheretheytethertransmembraneproteinstothespectrin cytoskeleton.Theobjectivesproposedare:toelucidateAnkR?sexpressionpatterns,functions,andmolecular interactionsinthebrain.
Aim1 willdeterminethetemporalandspatialexpressionofAnkRinthebrain.By analysisofAnkRthroughpostnataldevelopmentIwillestablishthetemporal,spatial,andcell-typespecific expression.
Aim2 willdeterminethecellularandbehavioralconsequencesofdisruptionofAnkRthrough analysisofanewAnkRconditionalknockoutmousemodel,whichallowsneuronalpopulationsofcellstobe studied,whilesparingerythroctes.ExaminationofphenotypeswillyieldkeyinsightsintoAnkRfunctioninthe nervoussystem.
Aim3 willdeterminethecytoskeletalandmembraneproteinsAnkRinteractswithinthe nervoussystem.Thiswillrevealthenormalproteinfunctionaswellasmechanisticinsightintothephenotypes resultingfromloss.CompletionofthesestudieswillrevealthefunctionofAnkRinthebrain,andenhanceour understandingofthemolecularmechanismsgoverningregionalproteinorganizationinthedeveloping,aging, anddiseasedbrain.BycomparingwhatIlearnaboutaboutAnkRtoAnkGandAnkB,Iwillresolvethe hypothesistoconcludeifAnkRfunctionsredundantly,orhasauniqueneuronalfunction.Moreover,data gainedfromtheseexperimentsmayalsoexplainAnkR?sroleinneurologicalconditionssuchasAlzheimer?s disease(AD),schizophrenia,andcerebellardysfunctioninwhichderegulationofAnkRhasbeenproposed.In total,completionoftheproposedexperimentswilldeterminetheroleofAnkRinnormalbrainfunction.

Public Health Relevance

. Ankryinproteinsarecriticalformembranedomainorganizationandproteinstabilizationinmanycelltypes throughoutthebody.However,littleisknownaboutthefunctionofAnkyrin-R(AnkR)inthenervoussystem. TheobjectiveofthisprojectistodeterminetheroleofAnkRinthebrainthroughdiscoveryofitsspatial, temporal,andcell-typespecificexpression,theconsequencesofitsdisruption,anditsinteractingproteins.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31NS100300-01A1
Application #
9393475
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Riddle, Robert D
Project Start
2017-06-01
Project End
2020-05-31
Budget Start
2017-06-01
Budget End
2018-05-31
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Neurosciences
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030