Mouse fibulin-2 gene -: Complete exon-intron organization and promoter characterization

被引:23
作者
Grässel, S
Sicot, FX
Gotta, S
Chu, ML
机构
[1] Thomas Jefferson Univ, Jefferson Inst Mol Med, Dept Dermatol & Cutaneous Biol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Jefferson Inst Mol Med, Dept Biochem & Mol Pharmacol, Philadelphia, PA 19107 USA
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1999年 / 263卷 / 02期
关键词
extracellular matrix; gene structure; promoter; regulatory element; alternative splicing;
D O I
10.1046/j.1432-1327.1999.00523.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
Fibulin-2, an extracellular matrix protein containing tandem arrays of calcium-binding epidermal growth factor-like motifs, is present in the basement membrane and stroma of many tissues. Its expression pattern suggested an essential role in organogenesis, particularly in embryonic heart development. In this study, we cloned the extreme 5' end of the mouse fibulin-2 cDNA, isolated phage and cosmid clones encoding the entire gene, and functionally characterized the promoter. The gene was found to consist of 18 exons spanning 55 kb of DNA. The exon-intron organization reflected the modular structure of the protein. Exon 9 was subjected to alternative splicing. All splice junctions conformed to the GT/AG rule, except that GC instead of GT was found in the splice donor site of exon 4. The gene lacked TATA and CAAT boxes but contained an initiator element (Inr) and several consensus Sp1 binding sites surrounding the transcription start sites. By transient transfection of promoter deletion constructs, a 0.46-kb region containing the clustered Sp1 sites was found to confer a high promoter activity.
引用
收藏
页码:471 / 477
页数:7
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