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CREB and Sp1 regulate the human MAP gene promoter activity in renal tubular epithelial cells
被引:6
|作者:
Lu, Chao
[1
]
Ren, Wei
[1
]
Su, Xing-Ming
[1
]
Chen, Jie-Qing
[1
]
Wu, Sheng-Hua
[1
]
Guo, Xi-Rong
[1
]
Huang, Song-Ming
[1
]
Chen, Long-Hua
[1
]
Zhou, Guo-Ping
[1
]
机构:
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Pediat, Nanjing 210029, Jiangsu, Peoples R China
基金:
中国博士后科学基金;
中国国家自然科学基金;
关键词:
CD2-associated protein (CD2AP);
cAMP-responsive element-binding protein(CREB) Stimulating protein 1 (Sp1);
promoter regulation;
transcriptional factor;
D O I:
10.1016/j.abb.2008.03.031
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The human CD2-associated protein (CD2AP) is involved in several molecular signaling pathways and is an important factor responsible for nephrotic syndrome. Here we report the identification of the transcription start point and promoter region of the human CD2AP gene in renal tubular epithelial cells. With luciferase assays and deletion analysis, we found that the region between -558 and -1 bp ahead of the transcription start point is indispensable for the promoter activity of the human CD2AP gene. A CREB site and two Sp1 sites were essential for maintaining the basal transcriptional activity of the human CD2AP promoter. Overexpression of phosphorylated CREB and Sp1 transactivated the human CD2AP promoter, whereas small interfering RNA-mediated blockage of CREB and Sp1 genes expressions inhibited markedly its activity. These findings provide the first analysis of the human CD2AP gene promoter and demonstrate that not only CREB but also Sp1 plays a critical role in regulating basal CD2AP promoter activity in renal tubular epithelial cells. (C) 2008 Elsevier Inc. All rights reserved.
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页码:143 / 149
页数:7
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