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dc.contributor.authorWELLMER, FRANKen
dc.date.accessioned2015-12-02T10:34:29Z
dc.date.available2015-12-02T10:34:29Z
dc.date.issued2014en
dc.date.submitted2014en
dc.identifier.citationPajoro, A., Madrigal, P., Muino, J.M., Matus, T., Jin, J., Mecchia, M.A., Debernardi, J.M., Palatnik, J.F., Balazadeh, S., Arif, M., O Maoileidigh, D.S., Wellmer, F., Krajewski, P., Riechmann, J.L., Angenent, G.C., and Kaufmann, K., Dynamics of chromatin accessibility and gene regulation by MADS-domain transcription factors in flower development., Genome Biology, 15, 2014, R41-en
dc.identifier.otherYen
dc.identifier.urihttp://hdl.handle.net/2262/75009
dc.descriptionPUBLISHEDen
dc.description.abstractBackground Development of eukaryotic organisms is controlled by transcription factors that trigger specific and global changes in gene expression programs. In plants, MADS-domain transcription factors act as master regulators of developmental switches and organ specification. However, the mechanisms by which these factors dynamically regulate the expression of their target genes at different developmental stages are still poorly understood. Results We characterized the relationship of chromatin accessibility, gene expression, and DNA binding of two MADS-domain proteins at different stages of Arabidopsis flower development. Dynamic changes in APETALA1 and SEPALLATA3 DNA binding correlated with changes in gene expression, and many of the target genes could be associated with the developmental stage in which they are transcriptionally controlled. We also observe dynamic changes in chromatin accessibility during flower development. Remarkably, DNA binding of APETALA1 and SEPALLATA3 is largely independent of the accessibility status of their binding regions and it can precede increases in DNA accessibility. These results suggest that APETALA1 and SEPALLATA3 may modulate chromatin accessibility, thereby facilitating access of other transcriptional regulators to their target genes. Conclusions Our findings indicate that different homeotic factors regulate partly overlapping, yet also distinctive sets of target genes in a partly stage-specific fashion. By combining the information from DNA-binding and gene expression data, we are able to propose models of stage-specific regulatory interactions, thereby addressing dynamics of regulatory networks throughout flower development. Furthermore, MADS-domain TFs may regulate gene expression by alternative strategies, one of which is modulation of chromatin accessibility.en
dc.description.sponsorshipThe authors would like to thank Christa Lanz, Markus Schmid, and Elio Schijlen for generating the Illumina GAII and Hiseq data, and Marjolein van Eenennaam and Marco Busscher for generating of the GRF8-GFP construct. We are grateful to Oriol Casagran for help with microarray hybridizations. Some parts of the computations were made at the Poznań Supercomputing and Networking Center. This work was supported by an NWO-VIDI grant to KK, and a Marie-Curie-ITN network grant SYSFLO (FP7/2007-2011, grant agreement no. 237909) to AP, PM, PK, and GCA. KK wishes to thank the Alexander-von-Humboldt foundation for support. This work was also supported by grants from Spanish Ministerio de Ciencia e Innovación (BFU2011-22734 to JLR). JTM and JJ were recipients of EMBO postdoctoral fellowshipsen
dc.format.extentR41en
dc.language.isoenen
dc.relation.ispartofseriesGenome Biologyen
dc.relation.ispartofseries15en
dc.rightsYen
dc.subjecteukaryotic organismsen
dc.subject.lcsheukaryotic organismsen
dc.titleDynamics of chromatin accessibility and gene regulation by MADS-domain transcription factors in flower development.en
dc.typeJournal Articleen
dc.contributor.sponsorScience Foundation Ireland (SFI)en
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/wellmerfen
dc.identifier.rssinternalid101282en
dc.identifier.doihttp://dx.doi.org/10.1186/gb-2014-15-3-r41en
dc.rights.ecaccessrightsopenAccess
dc.subject.TCDThemeGenes & Societyen
dc.subject.TCDTagGeneticsen
dc.subject.TCDTagGenomes, Genomicsen


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