Complex interactions at a GC-rich domain regulate cell type-dependent activity of the ornithine decarboxylase promoter

• Published in: The Journal of biological chemistry 1994-03, Vol.269 (11), p.7941-7949
• Main Authors: Li, R S, Abrahamsen, M S, Johnson, R R, Morris, D R
• Format: Article
• Language: English
• Subjects: Animals; Base Composition; Base Sequence; Binding Sites; Biological and medical sciences; Cell Line; Cell Nucleus - metabolism; Deoxyribonuclease I; Fundamental and applied biological sciences. Psychology; Gene Expression Regulation, Enzymologic; Humans; Molecular and cellular biology; Molecular genetics; Molecular Sequence Data; Mutagenesis, Site-Directed; Ornithine Decarboxylase - biosynthesis; Ornithine Decarboxylase - genetics; Promoter Regions, Genetic; Sp1 Transcription Factor - metabolism; Transcription. Transcription factor. Splicing. Rna processing; Tumor Cells, Cultured
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/s0021-9258(17)37142-9

Regulation of ornithine decarboxylase (ODC) is critical to the control of cellular growth, differentiation, and carcinogenesis. A GC-rich region in the ODC promoter contains two overlapping protein binding sites that interact to regulate basal level expression in some cell types. A perfect binding motif for transcription factor Sp1 (CCCCGCCCC) is located at nucleotides -114 to -106 relative to the site of transcriptional initiation, binds strongly to purified Sp1 protein, and forms several complexes when incubated with nuclear extracts. Only one of these complexes is recognized by Sp1-specific antibody. A new protein-binding motif (GCCCCTCCCC, located at -110 to -100) partially overlaps with the Sp1 site and analyses by DNase I protection showed that a new protein ("NF-ODC1") and the Sp1-like proteins interact with the ODC promoter in a mutually exclusive manner. Mutation of the NF-ODC1 binding motif strongly enhanced ODC promoter strength in some cell types, but had little or no influence in others. The effect of mutating the Sp1 site also varied with cell type. These cell type specificities did not correlate with the levels of Sp1 and NF-ODC1 binding activities in nuclear extracts. These results show that regulation of the ODC promoter by the Sp1 family is cell type-specific and modulated by a negative effector that we have termed NF-ODC1.