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Mol. Cell. Biol., Mar 1995, 1192-1202, Vol 15, No. 3
N Timchenko, DR Wilson, LR Taylor, S Abdelsayed, M Wilde, M Sawadogo and GJ Darlington
The human C/EBP alpha gene promoter shares significant sequence homology
with that of the mouse but has a different mechanism of autoregulation.
Activation of the murine promoter by direct binding of C/EBP alpha to a
site within 200 bp of the transcriptional start was shown to elevate
activity by approximately threefold (R. J. Christy, K. H. Kaestner, D. E.
Geiman, and M. D. Lane, Proc. Natl. Acad. Sci. USA 88:2593-2597, 1991; K.
Legraverend, P. Antonson, P. Flodby, and K. G. Xanthapoulos, Nucleic Acids
Res. 21:1735-1742, 1993). Unlike its murine counterpart, the human C/EBP
alpha gene promoter does not contain a cis element that binds the C/EBP
alpha protein. Neither C/EBP alpha nor C/EBP beta (NF-Il-6) binds the human
C/EBP alpha promoter within 437 bp. However, cotransfection studies show
that C/EBP alpha stimulates transcription of a reporter gene driven by 437
bp of the C/EBP alpha promoter. Our studies show that the human C/EBP alpha
protein stimulates USF to bind to a USF consensus element within C/EBP
alpha promoter and activates it by two- to threefold. We propose that the
human gene employs the ubiquitously expressed DNA-binding protein factor
USF to carry out autoregulation. Autoregulation of the human C/EBP alpha
promoter was abolished by deletion of the USF binding site, CACGTG.
Expression of human C/EBP beta following transfection did not stimulate USF
binding. These studies suggest a mechanism whereby tissue- specific
autoregulation can be achieved via a trans-acting factor that is expressed
in all cell types. Thus, direct binding of the C/EBP alpha protein to the
promoter of the C/EBP alpha gene is not required for autoregulation.
Copyright © 1995, American Society for Microbiology
Autoregulation of the human C/EBP alpha gene by stimulation of upstream stimulatory factor binding
Department of Pathology, Baylor College of Medicine, Houston, Texas.
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