The stacked-X DNA Holliday junction and protein recognition |
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Authors: | Khuu Patricia A Voth Andrea Regier Hays Franklin A Ho P Shing |
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Affiliation: | Department of Biochemistry and Biophysics, Oregon State University, Corvallis, OR 97331-7305, USA. |
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Abstract: | The crystal structure of the four-stranded DNA Holliday junction has now been determined in the presence and absence of junction binding proteins, with the extended open-X form of the junction seen in all protein complexes, but the more compact stacked-X structure observed in free DNA. The structures of the stacked-X junction were crystallized because of an unexpected sequence dependence on the stability of this structure. Inverted repeat sequences that contain the general motif NCC or ANC favor formation of stacked-X junctions, with the junction cross-over occurring between the first two positions of the trinucleotides. This review focuses on the sequence dependent structure of the stacked-X junction and how it may play a role in structural recognition by a class of dimeric junction resolving enzymes that themselves show no direct sequence recognition. |
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Keywords: | recombination Holliday junction resolvases protein recongnition DNA |
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