Nuclear Factor 1 Interferes with Sp1 Binding through a Composite Element on the Rat Poly(ADP-ribose) Polymerase Promoter to Modulate Its Activity in Vitro

• Published in: The Journal of biological chemistry 2001-06, Vol.276 (23), p.20766-20773
• Main Authors: Laniel, Marc-André, Poirier, Guy G., Guérin, Sylvain L.
• Format: Article
• Language: English
• Subjects: Animals; Base Sequence; CCAAT-Enhancer-Binding Proteins - metabolism; Cell Line; DNA; DNA Footprinting; DNA-Binding Proteins; Down-Regulation; Drosophila; Electrophoresis - methods; In Vitro Techniques; Molecular Sequence Data; NFI Transcription Factors; nuclear factor 1; Nuclear Proteins; PARP-1 gene; Pituitary Gland - cytology; Pituitary Gland - enzymology; Pituitary Gland - metabolism; Poly(ADP-ribose) Polymerases - genetics; Poly(ADP-ribose) Polymerases - metabolism; poly(ADP-ribose)polymerase 1; Promoter Regions, Genetic; Protein Binding; Rats; Recombinant Proteins - genetics; Recombinant Proteins - metabolism; Sp1 Transcription Factor - metabolism; Transcription Factors; Y-Box-Binding Protein 1
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M010360200

Poly(ADP-ribose) polymerase-1 (PARP-1) catalyzes the rapid and extensive poly(ADP-ribosyl)ation of nuclear proteins in response to DNA strand breaks, and its expression, although ubiquitous, is modulated from tissue to tissue and during cellular differentiation. PARP-1 gene promoters from human, rat, and mouse have been cloned, and they share a structure common to housekeeping genes, as they lack a functional TATA box and contain multiple GC boxes, which bind the transcriptional activator Sp1. We have previously shown that, although Sp1 is important for rat PARP1 (rPARP) promoter activity, its finely tuned modulation is likely dependent on other transcription factors that bind the rPARP proximal promoter in vitro. In this study, we identified one such factor as NF1-L, a rat liver isoform of the nuclear factor 1 family of transcription factors. The NF1-L site on the rPARP promoter overlaps one of the Sp1 binding sites previously identified, and we demonstrated that binding of both factors to this composite element is mutually exclusive. Furthermore, we provide evidence that NF1-L has no effect by itself on rPARP promoter activity, but rather down-regulates the Sp1 activity by interfering with its ability to bind the rPARP promoter in order to modulate transcription of the rPARP gene.