4.8 Article

The B-box dominates SAP-1-SRF interactions in the structure of the ternary complex

期刊

EMBO JOURNAL
卷 20, 期 12, 页码 3018-3028

出版社

WILEY
DOI: 10.1093/emboj/20.12.3018

关键词

crystal structure; gene regulation; serum response factor; transcription complex; X-ray crystallography

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The serum response element (SRE) is found in several immediate-early gene promoters. This DNA sequence is necessary and sufficient for rapid transcriptional induction of the human c-fos proto-oncogene in response to stimuli external to the cell. Full activation of the SRE requires the cooperative binding of a ternary complex factor (TCF) and serum response factor (SRF) to their specific DNA sites. The X-ray structure of the human SAP-1-SRF-SRE DNA ternary complex was determined (Protein Data Bank code 1hbx). It shows SAP-1 TCF bound to SRF through interactions between the SAP-1 B-box and SRE MADS domain in addition to contacts between their respective DNA-binding motifs, The SAP-1 B-box is part of a flexible linker of which 21 amino acids become ordered upon ternary complex formation. Comparison with a similar region from the yeast MAT alpha2-MCM1-DNA complex suggests a common binding motif through which MADS-box proteins may interact with additional factors such as Fli-1.

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