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.1991 May 1;88(9):3720-4.
doi: 10.1073/pnas.88.9.3720.

Cross-family dimerization of transcription factors Fos/Jun and ATF/CREB alters DNA binding specificity

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Cross-family dimerization of transcription factors Fos/Jun and ATF/CREB alters DNA binding specificity

T Hai et al. Proc Natl Acad Sci U S A..

Abstract

The Fos/Jun and ATF/CREB families of transcription factors function in coupling extracellular signals to alterations in expression of specific target genes. Like many eukaryotic transcription factors, these proteins bind to DNA as dimers. Dimerization is mediated by a structure known as the "leucine-zipper" motif. Although Fos/Jun and ATF/CREB were previously thought to interact preferentially with different DNA regulatory elements (the AP-1/TRE and ATF/CRE sites, respectively), we find that members of these two families form selective cross-family heterodimers. The resulting heterodimers display distinguishable DNA binding specificities from each other and from their parental homodimers. These findings indicate that the Fos/Jun and ATF/CREB families of transcription factors are not as distinct as was previously thought. We suggest that they can be grouped into a superfamily of transcription factors.

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References

    1. Nature. 1989 Feb 23;337(6209):749-52 - PubMed
    1. Cell. 1984 Feb;36(2):259-68 - PubMed
    1. Science. 1989 Mar 31;243(4899):1695-9 - PubMed
    1. Genes Dev. 1989 Feb;3(2):173-84 - PubMed
    1. Oncogene. 1990 Mar;5(3):295-302 - PubMed

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