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Mol. Cell. Biol., Apr 1996, 1367-1375, Vol 16, No. 4
X Luo and M Sawadogo
USF is a family of basic helix-loop transcriptional factors that recognizes
DNA-binding sites similar to those of the Myc oncoproteins. Here, various
functional domains in the mouse USF2 protein were identified and
characterized. Indirect immunofluorescence studies with transiently
transfected cells revealed that both the basic region and the highly
conserved USF-specific region (USR) are involved in the nuclear
localization of USF2. Cotransfection assays with deletion mutants
containing the DNA-binding domain of either USF2 or GAL4 identified two
distinct transcriptional activation domains in USF2, the USR and the exon
5-encoded region. Activity of the exon 5 activation domain was detectable
in both assay systems. Within USF2, however, its potency varied with the
conformation induced by the surrounding regions, especially that encoded by
alternatively spliced exon 4. In contrast, the USR activated transcription
only in its natural context upstream of the USF2 basic region and only with
reporter constructs containing the adenovirus major late minimal promoter
but not the E1b minimal promoter. However, insertion of an initiator
element downstream of the TATA box rescued the activity of the USR on the
E1b-driven reporters. The USR therefore represents a new type of activation
domain whose function depends very strongly on the core promoter context.
Copyright © 1996, American Society for Microbiology
Functional domains of the transcription factor USF2: atypical nuclear localization signals and context-dependent transcriptional activation domains
Department of Molecular Genetics, The University of Texas M.D. Anderson Cancer Center, Houston, 77030, USA.
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