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CELL-SPECIFIC EXPRESSION OF THE MOUSE GLIAL FIBRILLARY ACIDIC PROTEIN GENE - IDENTIFICATION OF THE CIS-ACTING AND TRANS-ACTING PROMOTER ELEMENTS FOR ASTROCYTE-SPECIFIC EXPRESSION
被引:132
|
作者
:
MIURA, M
论文数:
0
引用数:
0
h-index:
0
机构:
OSAKA UNIV,INST PROT RES,DIV REGULAT MACROMOLEC FUNCT,3-2 YAMADAOKA,SUITA,OSAKA 565,JAPAN
MIURA, M
TAMURA, T
论文数:
0
引用数:
0
h-index:
0
机构:
OSAKA UNIV,INST PROT RES,DIV REGULAT MACROMOLEC FUNCT,3-2 YAMADAOKA,SUITA,OSAKA 565,JAPAN
TAMURA, T
MIKOSHIBA, K
论文数:
0
引用数:
0
h-index:
0
机构:
OSAKA UNIV,INST PROT RES,DIV REGULAT MACROMOLEC FUNCT,3-2 YAMADAOKA,SUITA,OSAKA 565,JAPAN
MIKOSHIBA, K
机构
:
[1]
OSAKA UNIV,INST PROT RES,DIV REGULAT MACROMOLEC FUNCT,3-2 YAMADAOKA,SUITA,OSAKA 565,JAPAN
[2]
NATL INST BASIC BIOL,DEPT BIOL REGULAT,DIV BEHAV & NEUROBIOL,OKAZAKI,AICHI 444,JAPAN
来源
:
JOURNAL OF NEUROCHEMISTRY
|
1990年
/ 55卷
/ 04期
关键词
:
Astrocytes;
Cell differentiation;
Recombinant DNA;
Transcription;
Transfection;
D O I
:
10.1111/j.1471-4159.1990.tb03123.x
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
:
Abstract: We have determined the whole promoter sequence and the transcriptional startpoint of the mouse glial fibrillary acidic protein (GFAP) gene and characterized the promoter function. We found that the cis elements for astrocyte specific expression are located within 256 bp from the transcription startpoint. We defined by DNase I footprinting assay three trans‐acting factor binding sites (GFI, GFII, and GFIII) using brain or C6 astrocytoma nuclear extracts. GFI, GFII, and GFIII have AP‐2, NFI, and cyclic AMP‐responsive element motifs, respectively. Mutations in GFII drastically decreased the promoter activity. Base substitution in GFI and GFIII abolished the cell‐specific expression, resulting in the GFAP promoter expression even in some non‐GFAP‐producing cells. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
收藏
页码:1180 / 1188
页数:9
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