TY - JOUR
T1 - EZH2 regulates neuroepithelium structure and neuroblast proliferation by repressing p21
AU - Akizu, Naiara
AU - García, María Alejandra
AU - Estarás, Conchi
AU - Fueyo, Raquel
AU - Badosa, Carmen
AU - De Cruz, Xavier La
AU - Martínez-Balbás, Marian A.
N1 - Publisher Copyright:
© 2016 The Authors.
PY - 2016/4
Y1 - 2016/4
N2 - The function of EZH2 as a transcription repressor is well characterized. However, its role during vertebrate development is still poorly understood, particularly in neurogenesis. Here, we uncover the role of EZH2 in controlling the integrity of the neural tube and allowing proper progenitor proliferation. We demonstrate that knocking down the EZH2 in chick embryo neural tubes unexpectedly disrupts the neuroepithelium (NE) structure, correlating with alteration of the Rho pathway, and reduces neural progenitor proliferation. Moreover, we use transcriptional profiling and functional assays to show that EZH2-mediated repression of p21WAF1/CIP1contributes to both processes. Accordingly, overexpression of cytoplasmic p21WAF1/CIP1induces NE structural alterations and p21WAF1/CIP1suppression rescues proliferation defects and partially compensates for the structural alterations and the Rho activity. Overall, our findings describe a new role of EZH2 in controlling the NE integrity in the neural tube to allow proper progenitor proliferation.
AB - The function of EZH2 as a transcription repressor is well characterized. However, its role during vertebrate development is still poorly understood, particularly in neurogenesis. Here, we uncover the role of EZH2 in controlling the integrity of the neural tube and allowing proper progenitor proliferation. We demonstrate that knocking down the EZH2 in chick embryo neural tubes unexpectedly disrupts the neuroepithelium (NE) structure, correlating with alteration of the Rho pathway, and reduces neural progenitor proliferation. Moreover, we use transcriptional profiling and functional assays to show that EZH2-mediated repression of p21WAF1/CIP1contributes to both processes. Accordingly, overexpression of cytoplasmic p21WAF1/CIP1induces NE structural alterations and p21WAF1/CIP1suppression rescues proliferation defects and partially compensates for the structural alterations and the Rho activity. Overall, our findings describe a new role of EZH2 in controlling the NE integrity in the neural tube to allow proper progenitor proliferation.
KW - Animals
KW - Cell Polarity
KW - Cell Proliferation
KW - Chick Embryo
KW - Cyclin-Dependent Kinase Inhibitor p21/genetics
KW - Enhancer of Zeste Homolog 2 Protein/metabolism
KW - Gene Expression Regulation, Developmental
KW - Humans
KW - Neural Stem Cells/cytology
KW - Neural Tube/cytology
KW - Neuroepithelial Cells/cytology
KW - Promoter Regions, Genetic/genetics
KW - Repressor Proteins/metabolism
UR - http://www.scopus.com/inward/record.url?scp=84964430206&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:000374746600004&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.1098/rsob.150227
DO - 10.1098/rsob.150227
M3 - Article
C2 - 27248655
SN - 2046-2441
VL - 6
SP - 150227
JO - Open Biology
JF - Open Biology
IS - 4
M1 - 150227
ER -