4r2d: Difference between revisions
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[[Category: Cheng, X | [[Category: Cheng, X]] | ||
[[Category: Hashimoto, H | [[Category: Hashimoto, H]] | ||
[[Category: Olanrewaju, Y O | [[Category: Olanrewaju, Y O]] | ||
[[Category: Wilson, G G | [[Category: Wilson, G G]] | ||
[[Category: Zhang, X | [[Category: Zhang, X]] | ||
[[Category: Zheng, Y | [[Category: Zheng, Y]] | ||
[[Category: Dna binding protein-dna complex]] | [[Category: Dna binding protein-dna complex]] | ||
[[Category: Transcription]] | [[Category: Transcription]] | ||
[[Category: Zinc finger]] | [[Category: Zinc finger]] | ||
Revision as of 13:57, 19 November 2014
Egr1/Zif268 zinc fingers in complex with formylated DNAEgr1/Zif268 zinc fingers in complex with formylated DNA
Structural highlights
Publication Abstract from PubMedIn mammalian DNA, cytosine occurs in several chemical forms, including unmodified cytosine (C), 5-methylcytosine (5mC), 5-hydroxymethylcytosine (5hmC), 5-formylcytosine (5fC), and 5-carboxylcytosine (5caC). 5mC is a major epigenetic signal that acts to regulate gene expression. 5hmC, 5fC, and 5caC are oxidized derivatives that might also act as distinct epigenetic signals. We investigated the response of the zinc finger DNA-binding domains of transcription factors early growth response protein 1 (Egr1) and Wilms tumor protein 1 (WT1) to different forms of modified cytosine within their recognition sequence, 5'-GCG(T/G)GGGCG-3'. Both displayed high affinity for the sequence when C or 5mC was present and much reduced affinity when 5hmC or 5fC was present, indicating that they differentiate primarily oxidized C from unoxidized C, rather than methylated C from unmethylated C. 5caC affected the two proteins differently, abolishing binding by Egr1 but not by WT1. We ascribe this difference to electrostatic interactions in the binding sites. In Egr1, a negatively charged glutamate conflicts with the negatively charged carboxylate of 5caC, whereas the corresponding glutamine of WT1 interacts with this group favorably. Our analyses shows that zinc finger proteins (and their splice variants) can respond in modulated ways to alternative modifications within their binding sequence. Wilms tumor protein recognizes 5-carboxylcytosine within a specific DNA sequence.,Hashimoto H, Olanrewaju YO, Zheng Y, Wilson GG, Zhang X, Cheng X Genes Dev. 2014 Sep 25. pii: gad.250746.114. PMID:25258363[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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