Transforming growth factor-b (TGF-b) increases steady-state mRNA levels of several extracellular matrix proteins in mineralized connective tissues. Bone sialoprotein (BSP) is a major constituent of the bone matrix, thought to initiate and regulate the formation of mineral crystals. To determine the
Identification of transcription factor in the promoter region of rat regucalcin gene: Binding of nuclear factor I-A1 to TTGGC motif
β Scribed by Hiroyuki Misawa; Masayoshi Yamaguchi
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 222 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0730-2312
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β¦ Synopsis
Abstract
Hepatic nuclear protein has been reported to bind specifically to the TTGGC sequence of the rat regucalcin gene promoter region in stimulating the promoter activity (Misawa and Yamaguchi [2000] Biochem. Biophys. Res. Commun. 279: 275β281). The present study was undertaken to identify transcription factor, which binds to TTGGC motif in the rat regucalcin gene promoter, using the yeast oneβhybrid system. The sequence between β525 and β504, which has been defined as a functional promoter element IIβb, was used as bait to screen a rat liver cDNA library. Two cDNA clones were identified as a nuclear factor IβA1 (NF1βA1). The results of gel mobility shift assay and mutation analysis using recombinant NF1βA1 protein showed that this protein could specifically bind to TTGGC motif of the IIβb oligonucleotide in promoter region. The expression of NF1βA1 mRNA was found in the liver, kidney, heart, spleen, and brain of rats. This study demonstrates that NF1βA1 is a transcription factor in stimulating the rat regucalcin gene promoter activity. J. Cell. Biochem. 84: 795β802, 2002. Β© 2002 WileyβLiss, Inc.
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