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Science 31 March 1989: Vol. 243. no. 4899, pp. 1689 - 1694 DOI: 10.1126/science.2494701
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Articles
Science, Vol 243, Issue 4899, 1689-1694
Copyright © 1989 by American Association for the Advancement of Science
Leucine repeats and an adjacent DNA binding domain mediate the formation of functional cFos-cJun heterodimers
R Turner
and
R Tjian
Howard Hughes Medical Institute, Department of Biochemistry, University of California, Berkeley 94720.
The discovery that the AP-1 family of enhancer binding factors includes a complex of the cellular Fos (cFos) and cellular Jun (cJun) proteins established a direct and important link between oncogenesis and transcriptional regulation. Homodimeric cJun protein synthesized in vitro is capable of binding selectively to AP-1 recognition sites, whereas the cFos polypeptide is not. When cotranslated, the cFos and cJun proteins can form a stable, heterodimeric complex with the DNA binding properties of AP-1/cJun. The related proteins Jun B and vJun are also able to form DNA binding complexes with cFos. Directed mutagenesis of the cFos protein reveals that a leucine repeat structure is required for binding to cJun, in a manner consistent with the proposed function of the "leucine zipper." A novel domain adjacent to, but distinct from, the leucine repeat of cFos is required for DNA binding by cFos-cJun heterodimers. Thus experimental evidence is presented that leucine repeats can mediate complex formation between heterologous proteins and that promotes further understanding of the molecular mechanisms underlying the function of two proto-oncogene products.
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