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Interplay of the E Box, the Cyclic AMP Response Element, and HTF4/HEB in Transcriptional Regulation of the Neurospecific, Neurotrophin-Inducible vgfGene†

Authors :
Di Rocco, Giuliana
Pennuto, Maria
Illi, Barbara
Canu, Nadia
Filocamo, Gessica
Trani, Eugenia
Rinaldi, Anna Maria
Possenti, Roberta
Mandolesi, Georgia
Sirinian, M. Isabella
Jucker, Richard
Levi, Andrea
Nasi, Sergio
Source :
Molecular and Cellular Biology; March 1997, Vol. 17 Issue: 3 p1244-1253, 10p
Publication Year :
1997

Abstract

vgfis a neurotrophin response-specific, developmentally regulated gene that codes for a neurosecretory polypeptide. Its transcription in neuronal cells is selectively activated by the neurotrophins nerve growth factor (NGF), brain-derived neurotrophic factor, and neurotrophin 3, which induce survival and differentiation, and not by epidermal growth factor. We studied a short region of the rat vgfpromoter which is essential for its regulated expression. A cyclic AMP response element (CRE) within this region is necessary for NGF induction of vgftranscription. Two sites upstream of CRE, an E box and a CCAAT sequence, bind nuclear protein complexes and are involved in transcriptional control. The E box has a dual role. It acts as an inhibitor in NIH 3T3 fibroblasts, together with a second E box located downstream, and as a stimulator in the NGF-responsive cell line PC12. By expression screening, we have isolated the cDNA for a basic helix-loop-helix transcription factor, a homolog of the HTF4/HEB E protein, that specifically binds the vgfpromoter E box. The E protein was present in various cell lines, including PC12 cells, and was a component of a multiprotein nuclear complex that binds the promoter in vitro. The E box and CRE cooperate in binding to this complex, which may be an important determinant for neural cell-specific expression.

Details

Language :
English
ISSN :
02707306 and 10985549
Volume :
17
Issue :
3
Database :
Supplemental Index
Journal :
Molecular and Cellular Biology
Publication Type :
Periodical
Accession number :
ejs62672578
Full Text :
https://doi.org/10.1128/MCB.17.3.1244