2022
DOI: 10.1016/j.jmb.2021.167404
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Family-wide Characterization of Methylated DNA Binding Ability of Arabidopsis MBDs

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Cited by 8 publications
(11 citation statements)
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“…The canonical MBDs bind to mCG and TG DNA by the conserved base-specific interactions between arginine residues and guanine base of mCG/TG dinucleotide, as well as electrostatic interactions with the negatively charged backbone phosphate of dsDNA [ 18 , 19 , 20 , 21 , 22 , 23 , 32 , 33 ]. Notwithstanding, sequence alignment revealed that R760 and R781, corresponding R166 and R188 of human MBD2, are conserved in the TAM domain of BAZ2B ( Figure 1 B).…”
Section: Resultsmentioning
confidence: 99%
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“…The canonical MBDs bind to mCG and TG DNA by the conserved base-specific interactions between arginine residues and guanine base of mCG/TG dinucleotide, as well as electrostatic interactions with the negatively charged backbone phosphate of dsDNA [ 18 , 19 , 20 , 21 , 22 , 23 , 32 , 33 ]. Notwithstanding, sequence alignment revealed that R760 and R781, corresponding R166 and R188 of human MBD2, are conserved in the TAM domain of BAZ2B ( Figure 1 B).…”
Section: Resultsmentioning
confidence: 99%
“…Thus, we speculate that these structural features might restrain R760 to point to the mCG dinucleotide, and also hamper the R760 to specifically bind to mCG dinucleotide as the R166 of MBD2 does ( Figure 4 C). Besides the arginine fingers, the loop connecting β1 and β2, and the α1 of MBD2 make contact with the sugar-phosphate backbone, which recently has been shown to be crucial for DNA binding [ 23 ]. However, there is a short loop between the β1 and β2 of the BAZ2B TAM domain, and it fails to form interaction with the DNA backbone (Figures 1 B and 4 D).…”
Section: Resultsmentioning
confidence: 99%
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“…The binding activity and specificity have not been established for AtMBD3, 9, 10, 12, and 13 ( Ito et al, 2003 ; Scebba et al, 2003 ; Grafi et al, 2007 ). Recently, it was demonstrated that AtMBD6 and AtMBD7 are actually readers for methylated DNA ( Wu et al, 2022 ). AtMBD5 and AtMBD6, which are closely related and may have redundant functions ( Berg et al, 2003 ), are recruited to chromatin by recognition of CG methylation to redundantly repress a subset of genes and transposons ( Ichino et al, 2021 ), or participate in the formation of HDAC complexes to modulate the chromatin structure and gene transcription ( Zemach et al, 2005 ).…”
Section: Introductionmentioning
confidence: 99%
“…MBD1, MBD2, and MBD4 form a monophyletic group (Supplementary Fig. 1a), and all three proteins contain the conserved MBD domain 8,[12][13][14][16][17][18] (Supplementary Fig. 1b).…”
mentioning
confidence: 99%