Understandingtheexactcell-typecompositioninthedifferentregionsofthehumanbrainisafundamentalstep whentryingtointegratephysiological,behavioral,neurochemicalandmoleculardata.Atpresent,although majorcategoriesofcell-typespresentinthehumanbrainhavebeendefinedthroughahandfulofspecific markers,thedifferentsubtypeswithinthesecategoriesaswellastheirlocationarefarfromunderstood. CytosineDNAmethylation(mC)isastableepigenomicsignaturethatpersistsinpost-mitoticcellsthroughout theirlifetime,definingtheircellularidentity.Openchromatinmarksgeneregulatoryelementsthatcontrolcell type-specificgeneexpressionpatterns.SinglecellDNAmethylationandopenchromatinprofileshavebeen successfullyusedtoidentifydenovodistinctcelltypesinheterogeneoustissuesincludingthebrain.ThisU01 aimstoproduceafirstversionofanepigenomiccellatlasatthesingle-celllevelacrossthehumanbrain. Multi-modalintegrationbetweenepigenomicandtranscriptomicsignatureswillallowtheidentificationofnew celltypesanduniquecell-typemarkersthatwillbecomeavailabletothecommunity.Epigenomicprofilingof humanbraincellspermitsthediscoveryofcelltype-specificregulatoryregions,whichwillfacilitatethe functionalanalysisofgeneticvariantsassociatedwithpsychiatricandneurologicaldisorders.
Brainfunctionarisesfromnetworksofcellsconnectedtoeachotherinneuralcircuits.ThegoalofthisU01 projectistounderstandtheidentityofthemanydifferentkindsofcellsinvariousregionsofthehumanbrain. Determiningthecellcompositionofthehumanbrainwillaidintheunderstandingofavarietyofhuman diseasessuchasschizophreniaorautismwheretheseneuralcircuitsmaybeabnormal.