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miR-294/miR-302 promotes proliferation, suppresses G1-S restriction point, and inhibits ESC differentiation through separable mechanisms.
Wang, Yangming; Melton, Collin; Li, Ya-Pu; Shenoy, Archana; Zhang, Xin-Xin; Subramanyam, Deepa; Blelloch, Robert.
Afiliação
  • Wang Y; Peking-Tsinghua Joint Center for Life Sciences, Institute of Molecular Medicine, Peking University, Beijing 100871, China. yangming.wang@pku.edu.cn
Cell Rep ; 4(1): 99-109, 2013 Jul 11.
Article em En | MEDLINE | ID: mdl-23831024
ABSTRACT
The miR-294 and miR-302 microRNAs promote the abbreviated G1 phase of the embryonic stem cell (ESC) cell cycle and suppress differentiation induced by let-7. Here, we evaluated the role of the retinoblastoma (Rb) family proteins in these settings. Under normal growth conditions, miR-294 promoted the rapid G1-S transition independent of the Rb family. In contrast, miR-294 suppressed the further accumulation of cells in G1 in response to nutrient deprivation and cell-cell contact in an Rb-dependent fashion. We uncovered five additional miRNAs (miR-26a, miR-99b, miR-193, miR-199a-5p, and miR-218) that silenced ESC self-renewal in the absence of other miRNAs, all of which were antagonized by miR-294 and miR-302. Four of the six differentiation-inducing miRNAs induced an Rb-dependent G1 accumulation. However, all six still silenced self-renewal in the absence of the Rb proteins. These results show that the miR-294/miR-302 family acts through Rb-dependent and -independent pathways to regulate the G1 restriction point and the silencing of self-renewal, respectively.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diferenciação Celular / MicroRNAs / Proliferação de Células / Pontos de Checagem da Fase G1 do Ciclo Celular Limite: Animals Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diferenciação Celular / MicroRNAs / Proliferação de Células / Pontos de Checagem da Fase G1 do Ciclo Celular Limite: Animals Idioma: En Ano de publicação: 2013 Tipo de documento: Article