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REL Domain of NFATc2 Binding to Five Types of DNA Using Protein Binding Microarrays

[Image: see text] NFATc2 is a DNA binding protein in the Rel family transcription factors, which binds a CGGAA motif better when both cytosines in the CG dinucleotide are methylated. Using protein binding microarrays (PBMs), we examined the DNA binding of NFATc2 to three additional types of DNA: sin...

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Autores principales: Ray, Sreejana, Tillo, Desiree, Durell, Stewart R., Khund-Sayeed, Syed, Vinson, Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906578/
https://www.ncbi.nlm.nih.gov/pubmed/33644537
http://dx.doi.org/10.1021/acsomega.0c04069
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author Ray, Sreejana
Tillo, Desiree
Durell, Stewart R.
Khund-Sayeed, Syed
Vinson, Charles
author_facet Ray, Sreejana
Tillo, Desiree
Durell, Stewart R.
Khund-Sayeed, Syed
Vinson, Charles
author_sort Ray, Sreejana
collection PubMed
description [Image: see text] NFATc2 is a DNA binding protein in the Rel family transcription factors, which binds a CGGAA motif better when both cytosines in the CG dinucleotide are methylated. Using protein binding microarrays (PBMs), we examined the DNA binding of NFATc2 to three additional types of DNA: single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA) with either 5-methylcytosine (5mC, M) or 5-hydroxymethylcytosine (5hmC, H) in one strand and a cytosine in the second strand. ATTTCCAC, the complement of the core GGAA motif, is better bound as ssDNA compared to dsDNA. dsDNA containing the 5-mer CGGAA with either 5mC or 5hmC in one DNA strand is bound stronger than CGGAA. In contrast, the reverse complement TTCCG is bound weaker when it contains 5mC. Analysis of the available NFATc2:dsDNA complexes rationalizes these PBM data.
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spelling pubmed-79065782021-02-26 REL Domain of NFATc2 Binding to Five Types of DNA Using Protein Binding Microarrays Ray, Sreejana Tillo, Desiree Durell, Stewart R. Khund-Sayeed, Syed Vinson, Charles ACS Omega [Image: see text] NFATc2 is a DNA binding protein in the Rel family transcription factors, which binds a CGGAA motif better when both cytosines in the CG dinucleotide are methylated. Using protein binding microarrays (PBMs), we examined the DNA binding of NFATc2 to three additional types of DNA: single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA) with either 5-methylcytosine (5mC, M) or 5-hydroxymethylcytosine (5hmC, H) in one strand and a cytosine in the second strand. ATTTCCAC, the complement of the core GGAA motif, is better bound as ssDNA compared to dsDNA. dsDNA containing the 5-mer CGGAA with either 5mC or 5hmC in one DNA strand is bound stronger than CGGAA. In contrast, the reverse complement TTCCG is bound weaker when it contains 5mC. Analysis of the available NFATc2:dsDNA complexes rationalizes these PBM data. American Chemical Society 2021-02-02 /pmc/articles/PMC7906578/ /pubmed/33644537 http://dx.doi.org/10.1021/acsomega.0c04069 Text en © 2021 American Chemical Society This is an open access article published under an ACS AuthorChoice License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Ray, Sreejana
Tillo, Desiree
Durell, Stewart R.
Khund-Sayeed, Syed
Vinson, Charles
REL Domain of NFATc2 Binding to Five Types of DNA Using Protein Binding Microarrays
title REL Domain of NFATc2 Binding to Five Types of DNA Using Protein Binding Microarrays
title_full REL Domain of NFATc2 Binding to Five Types of DNA Using Protein Binding Microarrays
title_fullStr REL Domain of NFATc2 Binding to Five Types of DNA Using Protein Binding Microarrays
title_full_unstemmed REL Domain of NFATc2 Binding to Five Types of DNA Using Protein Binding Microarrays
title_short REL Domain of NFATc2 Binding to Five Types of DNA Using Protein Binding Microarrays
title_sort rel domain of nfatc2 binding to five types of dna using protein binding microarrays
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906578/
https://www.ncbi.nlm.nih.gov/pubmed/33644537
http://dx.doi.org/10.1021/acsomega.0c04069
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