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The retinal determination gene dachshund restricts cell proliferation by limiting the activity of the Homothorax-Yorkie complex

dc.contributor.authorBras-Pereira, C.
dc.contributor.authorCasares, F.
dc.contributor.authorJanody, F.
dc.date.accessioned2015-11-17T11:59:10Z
dc.date.available2015-11-17T11:59:10Z
dc.date.issued2015-04-15
dc.description.abstractThe Drosophila transcriptional co-activator protein Yorkie and its vertebrate orthologs YAP and TAZ are potent oncogenes, whose activity is normally kept in check by the upstream Hippo kinase module. Upon its translocation into the nucleus, Yorkie forms complexes with several tissue-specific DNA-binding partners, which help to define the tissue-specific target genes of Yorkie. In the progenitor cells of the eye imaginal disc, the DNA-binding transcription factor Homothorax is required for Yorkie-promoted proliferation and survival through regulation of the bantam microRNA (miRNA). The transit from proliferating progenitors to cell cycle quiescent precursors is associated with the progressive loss of Homothorax and gain of Dachshund, a nuclear protein related to the Sno/Ski family of co-repressors. We have identified Dachshund as an inhibitor of Homothorax-Yorkie-mediated cell proliferation. Loss of dachshund induces Yorkie-dependent tissue overgrowth. Conversely, overexpressing dachshund inhibits tissue growth, prevents Yorkie or Homothorax-mediated cell proliferation of disc epithelia and restricts the transcriptional activity of the Yorkie-Homothorax complex on the bantam enhancer in Drosophila cells. In addition, Dachshund collaborates with the Decapentaplegic receptor Thickveins to repress Homothorax and Cyclin B expression in quiescent precursors. The antagonistic roles of Homothorax and Dachshund in Yorkie activity, together with their mutual repression, ensure that progenitor and precursor cells are under distinct proliferation regimes. Based on the crucial role of the human dachshund homolog DACH1 in tumorigenesis, our work suggests that DACH1 might prevent cellular transformation by limiting the oncogenic activity of YAP and/or TAZ.pt_PT
dc.description.sponsorshipSpanish Ministry of Economy and Competitiveness (MINECO), EU Feder Funds: (BFU2012-34324), Consolider 'From Genes to Shape' (MICINN), FCT fellowships: (SFRH/BPD/46983/2008, IF/01031/2012).pt_PT
dc.identifier.citationThe retinal determination gene dachshund restricts cell proliferation by limiting the activity of the Homothorax-Yorkie complex Catarina Brás-Pereira, Fernando Casares, Florence Janody Development 2015 142: 1470-1479; doi: 10.1242/dev.113340pt_PT
dc.identifier.doi10.1242/dev.113340pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.7/495
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherCompany of Biologistspt_PT
dc.relationMolecular control of actin dynamics and change in cell shape in the morphogenetic furrow during Drosophila eye development.
dc.relation.publisherversionhttp://dev.biologists.org/content/142/8/1470pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectDachshundpt_PT
dc.subjectYorkiept_PT
dc.subjectHomothoraxpt_PT
dc.subjectDrosophila eye developmentpt_PT
dc.subjectProgenitor proliferationpt_PT
dc.subjectOrgan growthpt_PT
dc.titleThe retinal determination gene dachshund restricts cell proliferation by limiting the activity of the Homothorax-Yorkie complexpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleMolecular control of actin dynamics and change in cell shape in the morphogenetic furrow during Drosophila eye development.
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FBIA-BCM%2F71674%2F2006/PT
oaire.citation.endPage1479pt_PT
oaire.citation.issue8pt_PT
oaire.citation.startPage1470pt_PT
oaire.citation.titleDevelopmentpt_PT
oaire.citation.volume142pt_PT
oaire.fundingStream3599-PPCDT
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isProjectOfPublication8f380cbd-bd87-44dd-8d3b-0c3a4eec25d0
relation.isProjectOfPublication.latestForDiscovery8f380cbd-bd87-44dd-8d3b-0c3a4eec25d0

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