| Autor: |
Crawford, Deborah R., Leahy, Patrick, Hu, Ching Y., Chaudhry, Ali, Gronostajski, Richard, Grossman, Gregory, Woods, Jason, Hakimi, Parvin, Roesler, William J., Hanson, Richard W. |
| Zdroj: |
Journal of Biological Chemistry; May 1998, Vol. 273 Issue: 22 p13387-13390, 4p |
| Abstrakt: |
Nuclear factor-I (NFI) binds to the phosphoenolpyruvate carboxykinase (GTP) (PEPCK) gene promoter immediately 5′ to the cAMP regulatory element (CRE). This suggests an interaction between NFI and factors that bind the CRE. Of the four NFI isoforms expressed in mammalian tissues, NFI-A and -B stimulate basal transcription from the PEPCK gene promoter in HepG2 cells, while NFI-C and -X are slightly inhibitory. All four NFI isoforms abrogate the 20-fold protein kinase Ac (PKAc)-mediated induction of transcription from the PEPCK gene promoter. Normal PKAc-mediated induction was noted when the CRE was moved 10 base pairs 3′ of its original location. However if the CRE was moved 5 base pairs 3′, placing it out of phase with the other elements in the promoter, or moved 5′ to −285 (the P3(I) site in the promoter), some PKA-mediated stimulation was lost. The NFI-C isoform effectively inhibited PKAc induction regardless of the relative positions of the CRE and the NFI binding sites. NFI-C also abrogated cAMP regulatory element-binding protein (CREB)-induced activity of wild type and mutant PEPCK promoters. There was some cooperativity in the binding of CREB and NFI to their respective binding sites but this did not appear to be physiologically important. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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