Overthepastdecades,theHippopathwayhasbeenrecognizedasacrucialsignalingpathwaythat controlsorganandtissuesize,byrestrictingcellproliferationandanti-apoptosis.TheHippopathwaycanbe regulatedbyawiderangeofextracellularsignaling,includingperceivedphysicalsignalsfromcell microenvironment(i.e.contactinhibition,cellpolarity,cytoskeleton-basedmechanicalcues),growth factors/mitogenichormones(i.e.LPAandS1PregulatedGPCRsignaling),andrecentlydiscoveredmetabolic status(i.e.energystress,hypoxia).Mechanistically,almostallthesestimuliorconditionsoperateYAPactivity throughLATS1/2kinases.ThemajorknowledgegapforcurrentHipposignalingcomesfromthe uncharacterizedmechanismforLATS1/2regulation.Theoverallobjectiveofthisproposalistoelucidatethe regulatorymechanismforLATS1/2kinasesinresponsetoHippoupstreamsignalingevents. ThedetailedregulatorymechanismforLATS1/2kinasescouldbecomplex,sincemultipleupstream kinasesincludingMST1/2,MAP4Ks,TAO1-3,areabletophosphorylateLATS1/2andrequiredforLATS1/2 activation.Itisstillunclearhowtheseidentifiedkinasesarecoordinatedtotransduceupstreamsignalingto activateLATS1/2.Besides,smallRhoGTPasetogetherwithF-actincansenseupstreamsignalingtomodulate LATS1/2activities,however,theunderlyingmechanismisalsolargelyunknown.Therefore,overthepastfew years,wehaveconductedaproteomicanalysisofthemajorcomponentsandregulatorsintheHippopathway topursuetheanswertothesequestions.Unfortunately,ourfindingsandfindingsfromotherlabsfailed identifyingsuchaputative?mediator?tofillthecurrentknowledgegapintheHippopathway.Unexpectedlyand excitingly,ourpreliminarystudieshavediscoveredphosphatidicacid(PA)anditrelatedlipidsignalingasa criticalsignalingaxisinvolvedintheHippopathwayregulation.PAcouldfunctionasasecondmessengerto directlyassociatewithLATS1/2kinasesandregulateLATS1/2activities.Remarkably,PA?slevelaswellasthe activityofPLD1,akeyenzymethatcatalyzesPAproduction,arebothdecreasedinresponsetotheHippo- activatingstimuliorconditions.Onthebasisoftheseobservations,wehypothesizedthatPLD1-PAaxiscould playacrucialroleinregulationofLATS1/2activities.Specifically,weproposeto1)determinetheroleofPAin YAPregulation,particularlyfocusingontheindependentroleofPAfromLPAinYAPactivation;?2)elucidate themechanismbywhichPAactivatesYAP.WewilldissecttheroleofPAinLATS1/2suppressionthroughits associationwithLATS1/2andNF2;?and3)investigatetheroleofPLD1-PAaxisinLATS1/2regulationin responsetoHippoupstreamsignaling.Collectively,ourproposedstudywillrevealacrucialregulatory mechanismtocontrolLATS1/2activationinresponsetotheHippoupstreamsignalingandconceptually advanceourunderstandingoftheHippopathwaybyfillingthisknowledgegap.

Public Health Relevance

TheHippopathway,whichisconservedfromDrosophilatomammals,hasbeenrecognizedasa crucialsignalingpathwaygoverningcellproliferationandapoptosis,twokeyeventsinvolvedintissue homeostasisandorgansizecontrol.Althoughseveralupstreamregulators,conservedkinasecascade,key downstreameffectorsandnucleartranscriptionalfactorshaveallbeenidentified,thedetailedregulatory mechanismsfortheHippopathwayremaintobeelucidated.Myproposedresearchwillfocusonanewlipid signalingbranchinregulationoftheHippopathway,whichwillprovideusanopportunitytouncoveradditional components/regulatorsforthisputativepathway.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM126048-01
Application #
9420093
Study Section
Molecular and Integrative Signal Transduction Study Section (MIST)
Program Officer
Melillo, Amanda A
Project Start
2018-02-01
Project End
2023-01-31
Budget Start
2018-02-01
Budget End
2019-01-31
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of California Irvine
Department
Anatomy/Cell Biology
Type
Schools of Arts and Sciences
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92617
Han, Han; Qi, Ruxi; Zhou, Jeff Jiajing et al. (2018) Regulation of the Hippo Pathway by Phosphatidic Acid-Mediated Lipid-Protein Interaction. Mol Cell 72:328-340.e8
Han, Han; Yang, Bing; Nakaoka, Hiroki J et al. (2018) Hippo signaling dysfunction induces cancer cell addiction to YAP. Oncogene 37:6414-6424
Jung, Youn-Sang; Wang, Wenqi; Jun, Sohee et al. (2018) Deregulation of CRAD-controlled cytoskeleton initiates mucinous colorectal cancer via ?-catenin. Nat Cell Biol 20:1303-1314
Jung, Youn-Sang; Jun, Sohee; Kim, Moon Jong et al. (2018) TMEM9 promotes intestinal tumorigenesis through vacuolar-ATPase-activated Wnt/?-catenin signalling. Nat Cell Biol 20:1421-1433