Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros








Base de dados
Intervalo de ano de publicação
1.
Cell Cycle ; 8(22): 3729-41, 2009 Nov 15.
Artigo em Inglês | MEDLINE | ID: mdl-19823043

RESUMO

microRNAs (miRNAs) regulate numerous physiological processes such as cell division and differentiation in many tissue types including stem cells. To probe the role that miRNAs play in regulating processes relevant to embryonic stem cell biology, we used RNA interference to silence DICER and DROSHA, the two main miRNA processing enzymes. Consistent with a role for miRNAs in maintaining normal stem cell division and renewal, we found that perturbation of miRNA pathway function in human embryonic stem cells (hESCs) attenuates cell proliferation. Normal cell growth can be partially restored by introduction of the mature miRNAs miR-195 and miR-372. These miRNAs regulate two tumor suppressor genes, respectively: WEE1, which encodes a negative G2/M kinase modulator of the CycB/CDK complex and CDKN1A, which encodes p21, a CycE/CDK cyclin dependent kinase inhibitor that regulates the G1/S transition. We show that in wild-type hESCs, WEE 1 levels control the rate of hESC division, whereas p21 levels must be maintained at a low level for hESC division to proceed. These data support a model for hESC cell cycle control in which miRNAs regulate negative cell cycle modulators at two phases of the cell cycle to ensure proper replenishment of the stem cell population.


Assuntos
Divisão Celular/fisiologia , Células-Tronco Embrionárias/fisiologia , MicroRNAs/metabolismo , Modelos Biológicos , Sequência de Bases , Western Blotting , Proteínas de Ciclo Celular/metabolismo , Divisão Celular/genética , Inibidor de Quinase Dependente de Ciclina p21/metabolismo , Células-Tronco Embrionárias/metabolismo , Humanos , MicroRNAs/genética , Análise em Microsséries , Dados de Sequência Molecular , Proteínas Nucleares/metabolismo , Oligonucleotídeos/genética , Proteínas Tirosina Quinases/metabolismo , Interferência de RNA , Ribonuclease III/genética
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA