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[Mechanisms regulating p21 gene expression by retinoic acid-induced gene G protein].
Zou, Qingping; Xu, Guiping; Zhuang, Likun; Zhang, Zhanglin; Yan, Weiwei; Zhang, Yingting; Lou, Yejiang; Tong, Jianhua.
Afiliação
  • Zou Q; Faculty of Medical Laboratory Science, State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China.
  • Xu G; Faculty of Medical Laboratory Science, State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China.
  • Zhuang L; Faculty of Medical Laboratory Science, State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China.
  • Zhang Z; Faculty of Medical Laboratory Science, State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China.
  • Yan W; Faculty of Medical Laboratory Science, State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China.
  • Zhang Y; Faculty of Medical Laboratory Science, State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China.
  • Lou Y; Faculty of Medical Laboratory Science, State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China.
  • Tong J; Faculty of Medical Laboratory Science, State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China. Email: jh_tong@126.com.
Zhonghua Zhong Liu Za Zhi ; 36(9): 657-61, 2014 Sep.
Article em Zh | MEDLINE | ID: mdl-25564054
ABSTRACT

OBJECTIVE:

To investigate the mechanisms by which retinoic acid-induced gene G (RIG-G) protein regulates p21 gene expression.

METHODS:

Western blot was used to detect the effects of RIG-G protein overexpression on p21 protein expression level in leukemia cell line NB4 cells and the phosphorylation of both c-Jun and JNK in U937 cells. The c-Jun expression plasmid and p21 gene promoter-containing reporter plasmid were co-transfected into 293T cells, to explore the regulatory effect of c-Jun protein on p21 gene expression by luciferase reporter assay.

RESULTS:

Western blot showed that the overexpression of RIG-G protein significantly upregulated p21 protein level in the NB4 cells, and the level of p21 protein largely increased along with the induction of endogenous RIG-G protein during the differentiation of NB4 cells treated by all-trans retinoic acid (ATRA). Moreover, the phosphorylation of both c-Jun and JNK decreased in RIG-G-overexpressing U937 cells while total c-Jun and JNK proteins remained unchanged. After using the JNK inhibitor SP600125 to block JNK phosphorylation, the level of c-Jun phosphorylation was still dramatically reduced in the RIG-G-overexpressing U937T-RIG-G cells, compared with the control U937T-pTRE cells. These results indicated that the inhibitory effect of Rig-G protein on c-Jun phosphorylation could not only be through the JNK pathway, but also via some JNK-independent pathways. Luciferase reporter assay showed that when 0.1, 0.5, 1.0 and 2.0 µg c-Jun-expressing plasmids were respectively transfected into 293T cells, compared with the empty vector-transfected group, the relative luciferase activities were (83.0 ± 1.7)%, (73.7 ± 0.7)%, (68.9 ± 0.9)% and (64.1 ± 0.9)%, indicating that the transcriptional activity of p21 gene could be inhibited by c-Jun protein.

CONCLUSIONS:

RIG-G protein may suppress the phosphorylation of c-Jun protein through different signal pathways, thereby increasing the expression of p21 gene, arresting the cell cycle and inhibiting the cell growth in U937 cells.
Assuntos
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Base de dados: MEDLINE Assunto principal: Tretinoína / Proteínas de Ligação ao GTP / Inibidor de Quinase Dependente de Ciclina p21 Idioma: Zh Ano de publicação: 2014 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Tretinoína / Proteínas de Ligação ao GTP / Inibidor de Quinase Dependente de Ciclina p21 Idioma: Zh Ano de publicação: 2014 Tipo de documento: Article