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Binding of 14-3-3 reader proteins to phosphorylated DNMT1 facilitates aberrant DNA methylation and gene expression

Mammalian DNA (cytosine-5) methyltransferase 1 (DNMT1) is essential for maintenance methylation. Phosphorylation of Ser143 (pSer143) stabilizes DNMT1 during DNA replication. Here, we show 14-3-3 is a reader protein of DNMT1pSer143. In mammalian cells 14-3-3 colocalizes and binds DNMT1pSer143 post-DN...

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Autores principales: Estève, Pierre-Olivier, Zhang, Guoqiang, Ponnaluri, V.K. Chaithanya, Deepti, Kanneganti, Chin, Hang Gyeong, Dai, Nan, Sagum, Cari, Black, Karynne, Corrêa, Ivan R., Bedford, Mark T., Cheng, Xiaodong, Pradhan, Sriharsa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770214/
https://www.ncbi.nlm.nih.gov/pubmed/26553800
http://dx.doi.org/10.1093/nar/gkv1162
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author Estève, Pierre-Olivier
Zhang, Guoqiang
Ponnaluri, V.K. Chaithanya
Deepti, Kanneganti
Chin, Hang Gyeong
Dai, Nan
Sagum, Cari
Black, Karynne
Corrêa, Ivan R.
Bedford, Mark T.
Cheng, Xiaodong
Pradhan, Sriharsa
author_facet Estève, Pierre-Olivier
Zhang, Guoqiang
Ponnaluri, V.K. Chaithanya
Deepti, Kanneganti
Chin, Hang Gyeong
Dai, Nan
Sagum, Cari
Black, Karynne
Corrêa, Ivan R.
Bedford, Mark T.
Cheng, Xiaodong
Pradhan, Sriharsa
author_sort Estève, Pierre-Olivier
collection PubMed
description Mammalian DNA (cytosine-5) methyltransferase 1 (DNMT1) is essential for maintenance methylation. Phosphorylation of Ser143 (pSer143) stabilizes DNMT1 during DNA replication. Here, we show 14-3-3 is a reader protein of DNMT1pSer143. In mammalian cells 14-3-3 colocalizes and binds DNMT1pSer143 post-DNA replication. The level of DNMT1pSer143 increased with overexpression of 14-3-3 and decreased by its depletion. Binding of 14-3-3 proteins with DNMT1pSer143 resulted in inhibition of DNA methylation activity in vitro. In addition, overexpression of 14-3-3 in NIH3T3 cells led to decrease in DNMT1 specific activity resulting in hypomethylation of the genome that was rescued by transfection of DNMT1. Genes representing cell migration, mobility, proliferation and focal adhesion pathway were hypomethylated and overexpressed. Furthermore, overexpression of 14-3-3 also resulted in enhanced cell invasion. Analysis of TCGA breast cancer patient data showed significant correlation for DNA hypomethylation and reduced patient survival with increased 14-3-3 expressions. Therefore, we suggest that 14-3-3 is a crucial reader of DNMT1pSer143 that regulates DNA methylation and altered gene expression that contributes to cell invasion.
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spelling pubmed-47702142016-02-29 Binding of 14-3-3 reader proteins to phosphorylated DNMT1 facilitates aberrant DNA methylation and gene expression Estève, Pierre-Olivier Zhang, Guoqiang Ponnaluri, V.K. Chaithanya Deepti, Kanneganti Chin, Hang Gyeong Dai, Nan Sagum, Cari Black, Karynne Corrêa, Ivan R. Bedford, Mark T. Cheng, Xiaodong Pradhan, Sriharsa Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Mammalian DNA (cytosine-5) methyltransferase 1 (DNMT1) is essential for maintenance methylation. Phosphorylation of Ser143 (pSer143) stabilizes DNMT1 during DNA replication. Here, we show 14-3-3 is a reader protein of DNMT1pSer143. In mammalian cells 14-3-3 colocalizes and binds DNMT1pSer143 post-DNA replication. The level of DNMT1pSer143 increased with overexpression of 14-3-3 and decreased by its depletion. Binding of 14-3-3 proteins with DNMT1pSer143 resulted in inhibition of DNA methylation activity in vitro. In addition, overexpression of 14-3-3 in NIH3T3 cells led to decrease in DNMT1 specific activity resulting in hypomethylation of the genome that was rescued by transfection of DNMT1. Genes representing cell migration, mobility, proliferation and focal adhesion pathway were hypomethylated and overexpressed. Furthermore, overexpression of 14-3-3 also resulted in enhanced cell invasion. Analysis of TCGA breast cancer patient data showed significant correlation for DNA hypomethylation and reduced patient survival with increased 14-3-3 expressions. Therefore, we suggest that 14-3-3 is a crucial reader of DNMT1pSer143 that regulates DNA methylation and altered gene expression that contributes to cell invasion. Oxford University Press 2016-02-29 2015-11-08 /pmc/articles/PMC4770214/ /pubmed/26553800 http://dx.doi.org/10.1093/nar/gkv1162 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Gene regulation, Chromatin and Epigenetics
Estève, Pierre-Olivier
Zhang, Guoqiang
Ponnaluri, V.K. Chaithanya
Deepti, Kanneganti
Chin, Hang Gyeong
Dai, Nan
Sagum, Cari
Black, Karynne
Corrêa, Ivan R.
Bedford, Mark T.
Cheng, Xiaodong
Pradhan, Sriharsa
Binding of 14-3-3 reader proteins to phosphorylated DNMT1 facilitates aberrant DNA methylation and gene expression
title Binding of 14-3-3 reader proteins to phosphorylated DNMT1 facilitates aberrant DNA methylation and gene expression
title_full Binding of 14-3-3 reader proteins to phosphorylated DNMT1 facilitates aberrant DNA methylation and gene expression
title_fullStr Binding of 14-3-3 reader proteins to phosphorylated DNMT1 facilitates aberrant DNA methylation and gene expression
title_full_unstemmed Binding of 14-3-3 reader proteins to phosphorylated DNMT1 facilitates aberrant DNA methylation and gene expression
title_short Binding of 14-3-3 reader proteins to phosphorylated DNMT1 facilitates aberrant DNA methylation and gene expression
title_sort binding of 14-3-3 reader proteins to phosphorylated dnmt1 facilitates aberrant dna methylation and gene expression
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770214/
https://www.ncbi.nlm.nih.gov/pubmed/26553800
http://dx.doi.org/10.1093/nar/gkv1162
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