An Evolutionarily Conserved SoxB-Hdac2 Crosstalk Regulates Neurogenesis in a Cnidarian

SoxB transcription factors and histone deacetylases (HDACs) are each major players in the regulation of neurogenesis, but a functional link between them has not been previously demonstrated. Here, we show that SoxB2 and Hdac2 act together to regulate neurogenesis in the cnidarian Hydractinia echinat...

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Main Authors: Hakima Flici, Christine E. Schnitzler, R. Cathriona Millane, Graham Govinden, Amy Houlihan, Stephanie D. Boomkamp, Sanbing Shen, Andreas D. Baxevanis, Uri Frank
Format: Article
Language:English
Published: Elsevier 2017-02-01
Series:Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124717300554
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author Hakima Flici
Christine E. Schnitzler
R. Cathriona Millane
Graham Govinden
Amy Houlihan
Stephanie D. Boomkamp
Sanbing Shen
Andreas D. Baxevanis
Uri Frank
author_facet Hakima Flici
Christine E. Schnitzler
R. Cathriona Millane
Graham Govinden
Amy Houlihan
Stephanie D. Boomkamp
Sanbing Shen
Andreas D. Baxevanis
Uri Frank
author_sort Hakima Flici
collection DOAJ
description SoxB transcription factors and histone deacetylases (HDACs) are each major players in the regulation of neurogenesis, but a functional link between them has not been previously demonstrated. Here, we show that SoxB2 and Hdac2 act together to regulate neurogenesis in the cnidarian Hydractinia echinata during tissue homeostasis and head regeneration. We find that misexpression of SoxB genes modifies the number of neural cells in all life stages and interferes with head regeneration. Hdac2 was co-expressed with SoxB2, and its downregulation phenocopied SoxB2 knockdown. We also show that SoxB2 and Hdac2 promote each other’s transcript levels, but Hdac2 counteracts this amplification cycle by deacetylating and destabilizing SoxB2 protein. Finally, we present evidence for conservation of these interactions in human neural progenitors. We hypothesize that crosstalk between SoxB transcription factors and Hdac2 is an ancient feature of metazoan neurogenesis and functions to stabilize the correct levels of these multifunctional proteins.
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spelling doaj.art-bef769dbf914420fac71931a0f6f6ee32022-12-21T23:32:37ZengElsevierCell Reports2211-12472017-02-011861395140910.1016/j.celrep.2017.01.019An Evolutionarily Conserved SoxB-Hdac2 Crosstalk Regulates Neurogenesis in a CnidarianHakima Flici0Christine E. Schnitzler1R. Cathriona Millane2Graham Govinden3Amy Houlihan4Stephanie D. Boomkamp5Sanbing Shen6Andreas D. Baxevanis7Uri Frank8Centre for Chromosome Biology (CCB), School of Natural Sciences, National University of Ireland, Galway H91 CF50, IrelandWhitney Laboratory for Marine Bioscience, University of Florida, St. Augustine, FL 32080, USACentre for Chromosome Biology (CCB), School of Natural Sciences, National University of Ireland, Galway H91 CF50, IrelandCentre for Chromosome Biology (CCB), School of Natural Sciences, National University of Ireland, Galway H91 CF50, IrelandCentre for Chromosome Biology (CCB), School of Natural Sciences, National University of Ireland, Galway H91 CF50, IrelandRegenerative Medicine Institute (REMEDI), National University of Ireland, Galway, Galway H91 CF50, IrelandRegenerative Medicine Institute (REMEDI), National University of Ireland, Galway, Galway H91 CF50, IrelandComputational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-8002, USACentre for Chromosome Biology (CCB), School of Natural Sciences, National University of Ireland, Galway H91 CF50, IrelandSoxB transcription factors and histone deacetylases (HDACs) are each major players in the regulation of neurogenesis, but a functional link between them has not been previously demonstrated. Here, we show that SoxB2 and Hdac2 act together to regulate neurogenesis in the cnidarian Hydractinia echinata during tissue homeostasis and head regeneration. We find that misexpression of SoxB genes modifies the number of neural cells in all life stages and interferes with head regeneration. Hdac2 was co-expressed with SoxB2, and its downregulation phenocopied SoxB2 knockdown. We also show that SoxB2 and Hdac2 promote each other’s transcript levels, but Hdac2 counteracts this amplification cycle by deacetylating and destabilizing SoxB2 protein. Finally, we present evidence for conservation of these interactions in human neural progenitors. We hypothesize that crosstalk between SoxB transcription factors and Hdac2 is an ancient feature of metazoan neurogenesis and functions to stabilize the correct levels of these multifunctional proteins.http://www.sciencedirect.com/science/article/pii/S2211124717300554nervous systemregenerationtranscription factorSoxBhistone deacetylaseHdac2Hydractiniaevolutioncnidarianeurogenesis
spellingShingle Hakima Flici
Christine E. Schnitzler
R. Cathriona Millane
Graham Govinden
Amy Houlihan
Stephanie D. Boomkamp
Sanbing Shen
Andreas D. Baxevanis
Uri Frank
An Evolutionarily Conserved SoxB-Hdac2 Crosstalk Regulates Neurogenesis in a Cnidarian
Cell Reports
nervous system
regeneration
transcription factor
SoxB
histone deacetylase
Hdac2
Hydractinia
evolution
cnidaria
neurogenesis
title An Evolutionarily Conserved SoxB-Hdac2 Crosstalk Regulates Neurogenesis in a Cnidarian
title_full An Evolutionarily Conserved SoxB-Hdac2 Crosstalk Regulates Neurogenesis in a Cnidarian
title_fullStr An Evolutionarily Conserved SoxB-Hdac2 Crosstalk Regulates Neurogenesis in a Cnidarian
title_full_unstemmed An Evolutionarily Conserved SoxB-Hdac2 Crosstalk Regulates Neurogenesis in a Cnidarian
title_short An Evolutionarily Conserved SoxB-Hdac2 Crosstalk Regulates Neurogenesis in a Cnidarian
title_sort evolutionarily conserved soxb hdac2 crosstalk regulates neurogenesis in a cnidarian
topic nervous system
regeneration
transcription factor
SoxB
histone deacetylase
Hdac2
Hydractinia
evolution
cnidaria
neurogenesis
url http://www.sciencedirect.com/science/article/pii/S2211124717300554
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