TY - JOUR
T1 - The homeodomain protein Pbx1 is involved in cAMP-dependent transcription of human CYP17
AU - Ogo, Atsushi
AU - Waterman, Michael R.
AU - McAllister, Janette
AU - Kagawa, Norio
N1 - Funding Information:
1 This work was supported by USPHS Grant DK28350 and Grants ES00267, 1R01HD33852-01, and FY94-0899 from the March of Dimes Birth Defects Foundation. 2 Present address: Third Department of Internal Medicine, Kyushu University Faculty of Medicine, Fukuoka, Fukuoka 812, Japan. 3To whom correspondence should be addressed. Fax: 615-322-4349. E-mail: [email protected].
PY - 1997/12/1
Y1 - 1997/12/1
N2 - Pbx1 is a homeodomain transcription factor involved in cAMP-dependent transcriptional regulation of the bovine CYP17 gene. In this study, we have investigated the involvement of Pbx1 in the transcriptional regulation of the human CYP17 gene. Although a sequence identical to previously determined Pbx- binding sites is not present in the promoter region of the human CYP17 gene, three putative Pbx-binding sites are identified by sequence similarity analysis. Coexpression of Pbx1 and a catalytic subunit of protein kinase A (PKA) greatly enhances reporter gene transcription via the 5'-flanking region of the human CYP17 gene. Upon gel shift analysis utilizing nuclear extracts from human adrenal H295R cells, one of the three putative Pbx1-binding sites, -250/-241 bp, shows the typical intense doublet observed with other Pbx- binding sites. 5'-Deletion analyses of the reporter construct containing this Pbx-binding site showed approximately sixfold induction by coexpression of Pbx1 and PKA compared to the basal transcription, suggesting that Pbx1 binds the -250/ -241 bp sequence and participates in cAMP-dependent regulation of the human CYP17 gene.
AB - Pbx1 is a homeodomain transcription factor involved in cAMP-dependent transcriptional regulation of the bovine CYP17 gene. In this study, we have investigated the involvement of Pbx1 in the transcriptional regulation of the human CYP17 gene. Although a sequence identical to previously determined Pbx- binding sites is not present in the promoter region of the human CYP17 gene, three putative Pbx-binding sites are identified by sequence similarity analysis. Coexpression of Pbx1 and a catalytic subunit of protein kinase A (PKA) greatly enhances reporter gene transcription via the 5'-flanking region of the human CYP17 gene. Upon gel shift analysis utilizing nuclear extracts from human adrenal H295R cells, one of the three putative Pbx1-binding sites, -250/-241 bp, shows the typical intense doublet observed with other Pbx- binding sites. 5'-Deletion analyses of the reporter construct containing this Pbx-binding site showed approximately sixfold induction by coexpression of Pbx1 and PKA compared to the basal transcription, suggesting that Pbx1 binds the -250/ -241 bp sequence and participates in cAMP-dependent regulation of the human CYP17 gene.
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U2 - 10.1006/abbi.1997.0372
DO - 10.1006/abbi.1997.0372
M3 - Article
C2 - 9390195
AN - SCOPUS:0031543341
SN - 0003-9861
VL - 348
SP - 226
EP - 231
JO - Archives of Biochemistry and Biophysics
JF - Archives of Biochemistry and Biophysics
IS - 1
ER -