Nucleic Acids Research, Vol 26, Issue 10 2298-2305, Copyright © 1998 by Oxford University Press
LA Tomky, JK Strauss-Soukup and LJ Maher 3rd
Previous electrophoretic experiments suggest that the AP-1 site in duplex
DNA bends in response to the pattern of amino acid charges distal to the
basic region in bound bZIP proteins. The extent and direction of apparent
DNA bending are consistent with the prediction that DNA will collapse
locally upon asymmetric phosphate charge neutralization. To prove that
asymmetric phosphate neutralization could produce the observed degree of
DNA bending, the present experiments partially substitute anionic phosphate
diesters in the AP-1 site with various numbers of neutral methylphosphonate
linkages. DNA bending is induced toward the neutralized face of DNA. The
degree of DNA bending induced by methylphosphonate substitution
(approximately 3.5 degrees per neutralized phosphate) is comparable to that
induced by GCN4 variants carrying increasing numbers of additional basic
amino acids. It is plausible, therefore, that asymmetric phosphate
neutralization is the cause of DNA bending in such complexes.
ARTICLES
Effects of phosphate neutralization on the shape of the AP-1 transcription factor binding site in duplex DNA
Department of Biochemistry and Molecular Biology, Mayo Foundation, Rochester, MN 55905, USA.
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