6JV3

Crystal structure of 5-hydoxylmethylcytosine containing decamer dsDNA

Summary for 6JV3

• Entry DOI: 10.2210/pdb6jv3/pdb
• Descriptor: DNA (5'-D(*CP*CP*AP*GP*(5HC)P*GP*CP*TP*GP*G)-3') (1 entity in total)
• Functional Keywords: 5-hydoxylmethylcytosine, duplex dna, dna
• Biological source: Homo sapiens
• Total number of polymer chains: 4
• Total formula weight: 12304.07

Authors

Zhang, L.,Wang, Y.X. (deposition date: 2019-04-15, release date: 2019-07-31, Last modification date: 2024-03-27)

Primary citation

Fu, T.,Liu, L.,Yang, Q.L.,Wang, Y.,Xu, P.,Zhang, L.,Liu, S.,Dai, Q.,Ji, Q.,Xu, G.L.,He, C.,Luo, C.,Zhang, L.
Thymine DNA glycosylase recognizes the geometry alteration of minor grooves induced by 5-formylcytosine and 5-carboxylcytosine.
Chem Sci, 10:7407-7417, 2019

PubMed Abstract: The dynamic DNA methylation-demethylation process plays critical roles in gene expression control and cell development. The oxidation derivatives of 5-methylcytosine (5mC) generated by Tet dioxygenases in the demethylation pathway, namely 5-hydroxymethylcytosine (5hmC), 5-formylcytosine (5fC), and 5-carboxylcytosine (5caC), could impact biological functions by altering DNA properties or recognition by potential reader proteins. Hence, in addition to the fifth base 5mC, 5hmC, 5fC, and 5caC have been considered as the sixth, seventh, and eighth bases of the genome. How these modifications would alter DNA and be specifically recognized remain unclear, however. Here we report that formyl- and carboxyl-modifications on cytosine induce the geometry alteration of the DNA minor groove by solving two high-resolution structures of a dsDNA decamer containing fully symmetric 5fC and 5caC. The alterations are recognized distinctively by thymine DNA glycosylase TDG its finger residue R275, followed by subsequent preferential base excision and DNA repair. These observations suggest a mechanism by which reader proteins distinguish highly similar cytosine modifications for potential differential demethylation in order to achieve downstream biological functions.

PubMed: 31489163
DOI: 10.1039/c9sc02807b

Experimental method

X-RAY DIFFRACTION (2.851 Å)