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Involvement of Sp1 in basal and retinoic acid induced transcription of the human tissue-type plasminogen activator gene

Authors
Journal
FEBS Letters
0014-5793
Publisher
Wiley Blackwell (John Wiley & Sons)
Publication Date
Volume
456
Issue
1
Identifiers
DOI: 10.1016/s0014-5793(99)00942-4
Keywords
  • Tissue-Type Plasminogen Activator
  • Promoter-Enhancer
  • Sp1
  • Retinoic Acid Receptor

Abstract

Abstract Transcription of the human tissue-type plasminogen activator (t-PA) gene is regulated by a multi-hormonal responsive enhancer at −7 kb. Transient co-transfections of Drosophila SL2 and human HT1080 fibrosarcoma cells with t-PA reporter constructs showed that Sp1 and Sp3 activate the t-PA promoter. Moreover Sp1 (but not Sp3) binding to the promoter is involved in induction by retinoic acid (RA), a response mediated through the enhancer. The role of Sp1 is specific, since mutation of the CRE element in the promoter did not affect response to RA. In contrast, the glucocorticoid induction mediated by the enhancer is independent of these Sp1 and CRE elements.

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