Abnormal gene expression during early placental development has been associated with adverse pregnancy outcomes. However, the transcriptional regulatory networks underlying normal placental development, includ- ing the transcription factors, the enhancers they bind to, and the genes they regulate, are unknown. Until this fundamentalgapisfilled,thevariantsingenomicDNAthatcauseaberrantgeneexpressionandleadtopreg- nancycomplicationscannotbeunderstood.Theapplicant?slong-termgoalistoidentifyglobalmechanismsby whichtranscriptionfactorsandenhancersworktogethertoregulateplacentaldevelopment.Theoverallobjec- tiveofthisapplicationistodefineandcharacterizetranscriptionalregulatorynetworksforprocessesthatoccur duringthreecriticaltimepointsofmouseplacentaldevelopment(embryonicdays7.5,8.5,and9.5),priortothe formationofthematureplacenta.Thecentralhypothesis,basedonpublishedandpreliminarydata,isthattime point-specific transcriptional regulatory networks regulate distinct processes during early placental develop- ment, and that disruption of transcription factors or enhancers central to these networks leads to abnormal trophoblastgeneexpression.Therationalefortheproposedresearchisthatunderstandingtheregulatorynet- worksunderlyingearlyplacentaldevelopmentwillenableearlydetectionandtreatmentofplacentaldisorders. The central hypothesis will be tested using three specific aims: (1) to define process-specific transcriptional regulatory networks during early placental development;? (2) to determine the mechanisms by which key TF- enhancerpairsregulategeneexpressioninmousetrophoblastsubtypes;?and(3)todeterminetherelationship between cis-regulation in mouse and human trophoblasts. To execute these aims, we will use an integrated approach, combining experimental genomics (RNA-Seq, ChIP-Seq, and ATAC-Seq), computational analysis (e.g. co-expression analysis, enhancer module analysis, and binding site predictions), and functional assays (e.g.ChIP,reporterassays,andsiRNAknockdown).
Each aimi ssupportedbyastrongscientificpremiseand preliminarydata,andeachmethodhasbeenestablishedeitherintheapplicant?slaborinthelabofamember of the research team. Completion of this project willresult in a global understanding ofthe transcriptional net- works regulating early placental development, and in an understanding of the mechanisms by which key TF- enhancerpairsregulategeneexpressioninmouseandhumantrophoblastcells.Theresearchproposedinthis application is innovative, in the applicant?s opinion, because it represents a new and substantive departure from the status quo by shifting focus to genome-scale identification and characterization of TF-enhancer net- worksthatregulatespecificprocessesduringplacentaldevelopment.Thiscontributionissignificantbecauseit will provide a new understanding of normal placental development, ultimately leading to the development of noveltherapeuticinterventionsforplacenta-associateddisorders.

Public Health Relevance

Theproposedresearchisrelevanttopublichealthbecausediscoveringtranscriptionalnetworksandtranscrip- tion factor-enhancer pairs regulating early placental development is expected to increase understanding ofnormal placental development, and thereby of the pathogenesis of placenta-associated disorders like preeclampsiaandintrauterinegrowthrestriction.Thisunderstandingwillultimatelyleadtonovelbiomarkerde- velopment or therapeutic interventions to help predict and prevent such disorders. Thus, the proposed research is relevant to the part of NICHD?s mission that pertains to obtaining fundamentalknowledgethatcontributestoensuringmotherandbabyarehealthyduringandafterpregnancy.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
1R01HD096083-01
Application #
9577208
Study Section
Pregnancy and Neonatology Study Section (PN)
Program Officer
Eisenberg, Esther
Project Start
2018-08-24
Project End
2023-05-31
Budget Start
2018-08-24
Budget End
2019-05-31
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Iowa State University
Department
Genetics
Type
Schools of Arts and Sciences
DUNS #
005309844
City
Ames
State
IA
Country
United States
Zip Code
50011