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Plant Molecular Biology

, Volume 45, Issue 1, pp 63–73 | Cite as

DNA-binding and dimerization preferences of Arabidopsis homeodomain-leucine zipper transcription factors in vitro

  • Henrik Johannesson
  • Yan Wang
  • Peter Engström
Article

Abstract

Homeodomain-leucine zipper (HDZip) proteins constitute a large family of transcription factors apparently unique to plants. In this report we characterize the DNA-binding and dimerization preferences in vitro of class I HDZip proteins. Using gel-exclusion chromatography and in vitro protein binding assays we demonstrate that the HDZip class I protein ATHB5 forms a homodimeric complex in solution. Consistent with this finding we have demonstrated the sequence-specific interaction of ATHB5 with a 9 bp pseudopalindromic DNA sequence, CAATNATTG, composed of two half-sites overlapping at a central position, by use of a PCR-assisted binding-site selection assay and competitive EMSA experiments. A majority of other known members of HDZip class I interacted with similar DNA sequences, but differed in their preference for A/T versus G/C in the central position of the binding site. Selective heterodimerization in vitro was demonstrated between ATHB5 and different class I HDZip proteins. Heterodimer formation between class I HDZip proteins is of potential functional significance for the integration of information from different signalling pathways in the control of plant development.

Arabidopsis thaliana homeobox homeodomain leucine zipper plant 

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Copyright information

© Kluwer Academic Publishers 2001

Authors and Affiliations

  • Henrik Johannesson
    • 1
  • Yan Wang
    • 1
  • Peter Engström
    • 1
  1. 1.Department of Evolutionary Biology, Physiological BotanyUppsalaSweden

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