The VGF gene encodes a secretory protein that is expressed in a cell type-restricted pattern in neuroendocrine cells and is up-regulated by nerve growth factor (NGF) in the rat pheochromocytoma PC12 cell line. Here we report the isolation and characterization of the 5'-terminal region of the human VGF gene. In addition to a TATA box and a CCAAT box located at canonical distances from the transcription start site, the human VGF promoter contains several consensus sequences for different transcription factors, including a cyclic AMP response element and an AP-I element, several GC boxes, and sequences homologous to other neuronal promoters. Transient transfection analysis demonstrates that 2.3 kb of the 5'-flanking sequence acts as a tissue-specific promoter, efficiently used only by neuronal cells that express endogenous VGF. Deletion analysis reveals that a positive regulatory region is located between nucleotides -458 to -204. Negative cis-acting elements that repress promoter activity in cell lines that do not normally express VGF are located between nucleotides -2,305 and -573 and between -458 and -204. The 5'-flanking region of the human VGF gene confers responsiveness to NGF, cyclic AMP, and phorbol ester treatment.

Canu, N., Possenti, R., Rinaldi, A., Trani, E., Levi, A. (1997). Molecular cloning and characterization of the human VGF promoter region. JOURNAL OF NEUROCHEMISTRY, 68(4), 1390-1399.

Molecular cloning and characterization of the human VGF promoter region

CANU, NADIA
;
POSSENTI, ROBERTA;
1997-01-01

Abstract

The VGF gene encodes a secretory protein that is expressed in a cell type-restricted pattern in neuroendocrine cells and is up-regulated by nerve growth factor (NGF) in the rat pheochromocytoma PC12 cell line. Here we report the isolation and characterization of the 5'-terminal region of the human VGF gene. In addition to a TATA box and a CCAAT box located at canonical distances from the transcription start site, the human VGF promoter contains several consensus sequences for different transcription factors, including a cyclic AMP response element and an AP-I element, several GC boxes, and sequences homologous to other neuronal promoters. Transient transfection analysis demonstrates that 2.3 kb of the 5'-flanking sequence acts as a tissue-specific promoter, efficiently used only by neuronal cells that express endogenous VGF. Deletion analysis reveals that a positive regulatory region is located between nucleotides -458 to -204. Negative cis-acting elements that repress promoter activity in cell lines that do not normally express VGF are located between nucleotides -2,305 and -573 and between -458 and -204. The 5'-flanking region of the human VGF gene confers responsiveness to NGF, cyclic AMP, and phorbol ester treatment.
1997
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore BIO/09 - FISIOLOGIA
English
VGF gene; secretory protein; tissue-specific transcription; cyclic AMP response element
nerve growth-factor; neuron-specific expression; upstream regulatory elements; hydroxylase gene requires; camp-response element; messenger-rna levels; sodium-channel gene; synapsin-i gene; silencer element; secretogranin-ii
Canu, N., Possenti, R., Rinaldi, A., Trani, E., Levi, A. (1997). Molecular cloning and characterization of the human VGF promoter region. JOURNAL OF NEUROCHEMISTRY, 68(4), 1390-1399.
Canu, N; Possenti, R; Rinaldi, A; Trani, E; Levi, A
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/56950
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