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J Biol Chem, Vol. 273, Issue 17, 10506-10514, April 24, 1998
From the Department of Biochemistry and Genetics, The Medical
School, University of Newcastle upon Tyne,
Newcastle upon Tyne, NE2 4HH, United Kingdom
Serum response elements (SREs) play important
roles in transforming extracellular signals into specific nuclear
responses. The SRE-binding protein, serum response factor (SRF), plays
a pivotal role in this process. Several transcription factors have been
shown to interact with SRF and thereby create distinct complexes with
different regulatory potentials. The ETS domain transcription factor
Elk-1 is one such protein and serves to integrate distinct mitogen-activated protein kinase cascades at SREs. Elk-1 uses a short
hydrophobic surface presented on the surface of an
Interaction of Transcription Factors with Serum Response
Factor
IDENTIFICATION OF THE Elk-1 BINDING SURFACE
-helix to
interact with SRF. In this study we have used site-directed mutagenesis
to identify residues in SRF that comprise the Elk-1 binding surface.
The Elk-1 binding surface is composed of residues that lie on a
hydrophobic surface-exposed groove located at the junction of the MADS
box and C-terminal SAM motif. Different residues are implicated in
interactions between SRF and the transcription factor Fli-1, indicating
that although some overlap with the Elk-1 binding surface occurs, their
interaction surfaces on SRF are distinct. Our data are consistent with
the hypothesis that the SRF DNA-binding domain acts as docking site for
multiple transcription factors that can bind to small surface-exposed
patches within this domain.
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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