EZH2 regulates neuroepithelium structure and neuroblast proliferation by repressing p21

被引:31
作者
Akizu, Naiara [1 ,4 ]
Alejandra Garcia, Maria [1 ]
Estaras, Conchi [1 ,5 ]
Fueyo, Raquel [1 ]
Badosa, Carmen [1 ]
de la Cruz, Xavier [2 ,3 ]
Martinez-Balbas, Marian A. [1 ]
机构
[1] CSIC, IBMB, Dept Mol Genom, E-08028 Barcelona, Spain
[2] VHIR, Passeig Vall Hebron 119, Barcelona 08035, Spain
[3] ICREA, Barcelona 08018, Spain
[4] Scripps Res Inst, Dorris Neurosci Ctr, La Jolla, CA 92037 USA
[5] Salk Inst Biol Studies, Regulatory Biol Lab, 10010 N Torrey Pines Rd, La Jolla, CA 92037 USA
关键词
EZH2; neuroblast proliferation; gene silencing; histone methylation; neural development; DEVELOPING SPINAL-CORD; HISTONE METHYLTRANSFERASE ACTIVITY; SERUM RESPONSE FACTOR; EMBRYONIC STEM-CELLS; GROUP PROTEIN EZH2; NEURAL CREST; RHO-GTPASES; DEVELOPMENTAL REGULATORS; MOUSE DEVELOPMENT; GENE-EXPRESSION;
D O I
10.1098/rsob.150227
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 p21(WAF1/CIP1) contributes to both processes. Accordingly, overexpression of cytoplasmic p21(WAF1/CIP1) induces NE structural alterations and p21(WAF1/CIP1) suppression 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.
引用
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页数:12
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