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dc.contributor.authorNeville, Megan C.
dc.contributor.authorNojima, Tetsuya
dc.contributor.authorAshley, Elizabeth
dc.contributor.authorParker, Darren J.
dc.contributor.authorWalker, John
dc.contributor.authorSouthall, Tony
dc.contributor.authorVan de Sande, Bram
dc.contributor.authorMarques, Ana C.
dc.contributor.authorFischer, Bettina
dc.contributor.authorBrand, Andrea H.
dc.contributor.authorRussell, Steven
dc.contributor.authorRitchie, Michael G.
dc.contributor.authorAerts, Stein
dc.contributor.authorGoodwin, Stephen F.
dc.date.accessioned2014-05-14T13:31:01Z
dc.date.available2014-05-14T13:31:01Z
dc.date.issued2014-02-03
dc.identifier103836593
dc.identifier29b4b2fa-15cc-41b1-86b9-8a04727a94c3
dc.identifier000330918900017
dc.identifier84895069924
dc.identifier000330918900017
dc.identifier.citationNeville , M C , Nojima , T , Ashley , E , Parker , D J , Walker , J , Southall , T , Van de Sande , B , Marques , A C , Fischer , B , Brand , A H , Russell , S , Ritchie , M G , Aerts , S & Goodwin , S F 2014 , ' Male-specific fruitless isoforms target neurodevelopmental genes to specify a sexually dimorphic nervous system ' , Current Biology , vol. 24 , no. 3 , pp. 229-241 . https://doi.org/10.1016/j.cub.2013.11.035en
dc.identifier.issn0960-9822
dc.identifier.otherORCID: /0000-0001-7913-8675/work/46761107
dc.identifier.urihttps://hdl.handle.net/10023/4790
dc.descriptionThis work was supported by grants from the Wellcome Trust to S.F.G. (WT085521MA and WT082987MF) and the Natural Environment Research Council to S.F.G and M.G.R. (NE/J023647/1). J.W. and E.A were supported by Biotechnology and Biological Sciences Research Council Committee studentships.en
dc.description.abstractBackground In Drosophila, male courtship behavior is regulated in large part by the gene fruitless (fru). fru encodes a set of putative transcription factors that promote male sexual behavior by controlling the development of sexually dimorphic neuronal circuitry. Little is known about how Fru proteins function at the level of transcriptional regulation or the role that isoform diversity plays in the formation of a male-specific nervous system. Results To characterize the roles of sex-specific Fru isoforms in specifying male behavior, we generated novel isoform-specific mutants and used a genomic approach to identify direct Fru isoform targets during development. We demonstrate that all Fru isoforms directly target genes involved in the development of the nervous system, with individual isoforms exhibiting unique binding specificities. We observe that fru behavioral phenotypes are specified by either a single isoform or a combination of isoforms. Finally, we illustrate the utility of these data for the identification of novel sexually dimorphic genomic enhancers and novel downstream regulators of male sexual behavior. Conclusions These findings suggest that Fru isoform diversity facilitates both redundancy and specificity in gene expression, and that the regulation of neuronal developmental genes may be the most ancient and conserved role of fru in the specification of a male-specific nervous system.
dc.format.extent13
dc.format.extent3303794
dc.language.isoeng
dc.relation.ispartofCurrent Biologyen
dc.subjectAntagonistic chromatin factorsen
dc.subjectZinc-finger proteinen
dc.subjectDrosophila-melanogasteren
dc.subjectCourtship songen
dc.subjectTranscription factorsen
dc.subjectNeural circuitryen
dc.subjectBehavioren
dc.subjectDifferentiationen
dc.subjectBrainen
dc.subjectOrientationen
dc.subjectQH426 Geneticsen
dc.subjectBDCen
dc.subjectR2Cen
dc.subject.lccQH426en
dc.titleMale-specific fruitless isoforms target neurodevelopmental genes to specify a sexually dimorphic nervous systemen
dc.typeJournal articleen
dc.contributor.sponsorNERCen
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.contributor.institutionUniversity of St Andrews. Centre for Biological Diversityen
dc.contributor.institutionUniversity of St Andrews. Institute of Behavioural and Neural Sciencesen
dc.identifier.doi10.1016/j.cub.2013.11.035
dc.description.statusPeer revieweden
dc.identifier.grantnumberNE/J020818/1en


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