MAP kinase/ERK kinase 1 (MEK1) phosphorylates regulator of calcineurin 1 (RCAN1) to regulate neuronal differentiation

被引:1
|
作者
Kim, Seon Sook [1 ]
Lee, Eun Hye [1 ]
Shin, Jin Hak [1 ]
Seo, Su Ryeon [1 ]
机构
[1] Kangwon Natl Univ, Dept Mol Biosci, Chunchon, South Korea
基金
新加坡国家研究基金会;
关键词
differentiation; Down syndrome; MEK1; NGF; RCAN1; SYNDROME CRITICAL REGION; ADRENAL PHEOCHROMOCYTOMA CELLS; DOWN-SYNDROME; PROTEIN-KINASE; CLONAL LINE; HUMAN-FETUS; DSCR1; INHIBITOR; EXPRESSION; GROWTH;
D O I
10.1002/jcp.30609
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Regulator of calcineurin 1 (RCAN1) is located close to the Down syndrome critical region (DSCR) on human chromosome 21 and is related to the Down syndrome (DS) phenotype. To identify a novel binding partner of RCAN1, we performed yeast two-hybrid screening and identified mitogen-activated protein (MAP) kinase/extracellular signal-regulated kinase (ERK) kinase 1 (MEK1) as a partner. MEK1 was able to bind and phosphorylate RCAN1 in vitro and in vivo. MEK1-dependent RCAN1 phosphorylation caused an increase in RCAN1 expression by increasing the protein half-life. Nerve growth factor (NGF)-dependent activation of the MEK1 pathway consistently induced RCAN1 expression. Moreover, we found that RCAN1 overexpression inhibited NGF-induced neurite outgrowth and expression of neuronal marker genes, such as growth cone-associated protein 43 (GAP43) and synapsin I, via inhibition of MEK1-ERK1/2 pathways. Our findings provide evidence that MEK1-dependent RCAN1 phosphorylation acts as an important molecular mechanism in the control of neuronal differentiation.
引用
收藏
页码:1406 / 1417
页数:12
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