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Transcriptional regulation of S100A1 and expression during mouse heart development
被引:36
作者:
Kiewitz, R
Lyons, GE
Schäfer, BW
Heizmann, CW
机构:
[1] Univ Zurich, Dept Pediat, Div Clin Chem & Biochem, CH-8032 Zurich, Switzerland
[2] Univ Wisconsin, Sch Med, Dept Anat, Madison, WI 53706 USA
来源:
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
|
2000年
/
1498卷
/
2-3期
关键词:
calcium-binding protein;
S100A1;
gene;
mouse heart development;
promoter analysis;
primary cardiomyocyte;
cardiac gene expression;
D O I:
10.1016/S0167-4889(00)00097-5
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:
S100A1, a member of the large EF-hand family of Ca2+-binding proteins, is mainly expressed in the mammalian heart. To assess the underlying mechanisms for cell- and tissue-specific expression we isolated and characterized the mouse S100A1 gene. The gene displays a high degree of homology to the human and rat genes, especially in the exonic sequences. In its promoter region and the first intron, we identified regulatory elements characteristic for cardiac and slow skeletal muscle restricted genes. Transfection assays with luciferase constructs containing different parts of the S100A1 gene demonstrated the active expression in primary mouse cardiomyocytes and that its 5'-upstream region containing a putative cardiac enhancer showed a greatly increased activity. Furthermore, we investigated the expression of the S100A1 mRNA during embryonic mouse development, using in situ hybridization. S100A1 transcripts were first detected in the primitive heart at embryonic day (E) 8, with equal levels in the atrium and ventricle. During development up to E17.5 we detected a shift in the S100A1 expression pattern with lower levels in atrial and high levels in ventricular myocardium. The regulatory elements identified in the mouse S100A1 promoter correspond well with the observed expression pattern and suggest that S100A1 has an important function during heart muscle development. (C) 2000 Elsevier Science B.V. All rights reserved.
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页码:207 / 219
页数:13
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