Abstract
Epidermal growth factor (EGF), determined by immunoprecipitation and Western blot analysis, increased both enzyme activity and protein level of 12-lipoxygenase in the solubilized microsomes of human epidermoid carcinoma A431 cells, respectively. The EGF-induced expression of 12-lipoxygenase mRNA was inhibited by transcription inhibitors such as actinomycin D and 5,6-dichlorobenzimidazole riboside. Promoters of different lengths for human 12-lipoxygenase gene were used to prepare the luciferase fusion vectors. These construct plasmids were transiently transfected into A431 cells, and the induction of luciferase expression by EGF was examined. A 4- to 6-fold increase in luciferase reporter activity stimulated by EGF for 18 h treatment was observed in plasmids with the 5'-flanking region length of -951 bp and that of -224 bp upstream from translation starting site. The time-dependent induction of luciferase activity by EGF paralleled the EGF-induced enzyme activity and expression of 12-lipoxygenase protein. Taken together, the results of this study indicate that EGF enhanced the transcription of the human 12-lipoxygenase gene, resulting in an increase in the amount and activity of 12-lipoxygenase.
Original language | English |
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Pages (from-to) | 38-46 |
Number of pages | 9 |
Journal | Biochimica et Biophysica Acta - Lipids and Lipid Metabolism |
Volume | 1344 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jan 7 1997 |
Externally published | Yes |
Keywords
- 12-Lipoxygenase
- Epidermal growth factor
- Human epidermoid carcinoma A431 cell
- Transcription
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Endocrinology