Journal of neurochemistry · 2011
Crx broadly modulates the pineal transcriptome.
СтатьяResearch Support, N.I.H., IntramuralПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Rovsing Louise, Clokie Samuel, Bustos Diego M, Rohde Kristian, Coon Steven L, Litman Thomas, Rath Martin F, Møller Morten, Klein David C
Аннотация
Cone-rod homeobox (Crx) encodes Crx, a transcription factor expressed selectively in retinal photoreceptors and pinealocytes, the major cell type of the pineal gland. In this study, the influence of Crx on the mammalian pineal gland was studied by light and electron microscopy and by use of microarray and qRTPCR technology, thereby extending previous studies on selected genes (Furukawa et al. 1999). Deletion of Crx was not found to alter pineal morphology, but was found to broadly modulate the mouse pineal transcriptome, characterized by a>2-fold down-regulation of 543 genes and a>2-fold up-regulation of 745 genes (p<0.05). Of these, one of the most highly up-regulated (18-fold) was Hoxc4, a member of the Hox gene family, members of which are known to control gene expression cascades. During a 24-h period, a set of 51 genes exhibited differential day/night expression in pineal glands of wild-type animals; only eight of these were also day/night expressed in the Crx⁻/⁻ pineal gland. However, in the Crx⁻/⁻ pineal gland 41 genes exhibited differential night/day expression that was not seen in wild-type animals. These findings indicate that Crx broadly modulates the pineal transcriptome and also influences differential night/day gene expression in this tissue. Some effects of Crx deletion on the pineal transcriptome might be mediated by Hoxc4 up-regulation.
Предметные рубрики MeSH
AnimalsCircadian RhythmCloning, MolecularComputational BiologyData Interpretation, StatisticalDown-RegulationGene DeletionGene Expression ProfilingHomeodomain ProteinsMiceMice, KnockoutMicroarray AnalysisMicroscopy, Electron, TransmissionPineal GlandReverse Transcriptase Polymerase Chain ReactionTrans-ActivatorsTranscription, Genetic