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MiRNA-128 regulates the proliferation and neurogenesis of neural precursors by targeting PCM1 in the developing cortex.
Zhang, Wei; Kim, Paul Jong; Chen, Zhongcan; Lokman, Hidayat; Qiu, Lifeng; Zhang, Ke; Rozen, Steven George; Tan, Eng King; Je, Hyunsoo Shawn; Zeng, Li.
Afiliação
  • Zhang W; Neural Stem Cell Research Lab, Research Department, National Neuroscience Institute, Singapore, Singapore.
  • Kim PJ; Molecular Neurophysiology Laboratory, Signature Program in Neuroscience and Behavioral Disorders, Duke-NUS Graduate Medical School, Singapore, Singapore.
  • Chen Z; Neural Stem Cell Research Lab, Research Department, National Neuroscience Institute, Singapore, Singapore.
  • Lokman H; Molecular Neurophysiology Laboratory, Signature Program in Neuroscience and Behavioral Disorders, Duke-NUS Graduate Medical School, Singapore, Singapore.
  • Qiu L; Neural Stem Cell Research Lab, Research Department, National Neuroscience Institute, Singapore, Singapore.
  • Zhang K; Neural Stem Cell Research Lab, Research Department, National Neuroscience Institute, Singapore, Singapore.
  • Rozen SG; Center for Computational Biology, Duke-NUS Graduate Medical School, Singapore, Singapore.
  • Tan EK; Department of Neurology, National Neuroscience Institute, Singapore, Singapore.
  • Je HS; Neuroscience and Behavioral Disorders program, Duke-NUS Graduate Medical School, Singapore, Singapore.
  • Zeng L; Molecular Neurophysiology Laboratory, Signature Program in Neuroscience and Behavioral Disorders, Duke-NUS Graduate Medical School, Singapore, Singapore.
Elife ; 52016 Feb 17.
Article em En | MEDLINE | ID: mdl-26883496
ABSTRACT
During the development, tight regulation of the expansion of neural progenitor cells (NPCs) and their differentiation into neurons is crucial for normal cortical formation and function. In this study, we demonstrate that microRNA (miR)-128 regulates the proliferation and differentiation of NPCs by repressing pericentriolar material 1 (PCM1). Specifically, overexpression of miR-128 reduced NPC proliferation but promoted NPC differentiation into neurons both in vivo and in vitro. In contrast, the reduction of endogenous miR-128 elicited the opposite effects. Overexpression of miR-128 suppressed the translation of PCM1, and knockdown of endogenous PCM1 phenocopied the observed effects of miR-128 overexpression. Furthermore, concomitant overexpression of PCM1 and miR-128 in NPCs rescued the phenotype associated with miR-128 overexpression, enhancing neurogenesis but inhibiting proliferation, both in vitro and in utero. Taken together, these results demonstrate a novel mechanism by which miR-128 regulates the proliferation and differentiation of NPCs in the developing neocortex.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diferenciação Celular / Córtex Cerebral / Regulação da Expressão Gênica / Proteínas de Ciclo Celular / MicroRNAs / Proliferação de Células / Células-Tronco Neurais Limite: Animals Idioma: En Revista: Elife Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Singapura

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diferenciação Celular / Córtex Cerebral / Regulação da Expressão Gênica / Proteínas de Ciclo Celular / MicroRNAs / Proliferação de Células / Células-Tronco Neurais Limite: Animals Idioma: En Revista: Elife Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Singapura