Cargando…

PGC7 suppresses TET3 for protecting DNA methylation

Ten-eleven translocation (TET) family enzymes convert 5-methylcytosine to 5-hydroxylmethylcytosine. However, the molecular mechanism that regulates this biological process is not clear. Here, we show the evidence that PGC7 (also known as Dppa3 or Stella) interacts with TET2 and TET3 both in vitro an...

Descripción completa

Detalles Bibliográficos
Autores principales: Bian, Chunjing, Yu, Xiaochun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950671/
https://www.ncbi.nlm.nih.gov/pubmed/24322296
http://dx.doi.org/10.1093/nar/gkt1261
_version_ 1782307028570472448
author Bian, Chunjing
Yu, Xiaochun
author_facet Bian, Chunjing
Yu, Xiaochun
author_sort Bian, Chunjing
collection PubMed
description Ten-eleven translocation (TET) family enzymes convert 5-methylcytosine to 5-hydroxylmethylcytosine. However, the molecular mechanism that regulates this biological process is not clear. Here, we show the evidence that PGC7 (also known as Dppa3 or Stella) interacts with TET2 and TET3 both in vitro and in vivo to suppress the enzymatic activity of TET2 and TET3. Moreover, lacking PGC7 induces the loss of DNA methylation at imprinting loci. Genome-wide analysis of PGC7 reveals a consensus DNA motif that is recognized by PGC7. The CpG islands surrounding the PGC7-binding motifs are hypermethylated. Taken together, our study demonstrates a molecular mechanism by which PGC7 protects DNA methylation from TET family enzyme-dependent oxidation.
format Online
Article
Text
id pubmed-3950671
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-39506712014-03-12 PGC7 suppresses TET3 for protecting DNA methylation Bian, Chunjing Yu, Xiaochun Nucleic Acids Res Ten-eleven translocation (TET) family enzymes convert 5-methylcytosine to 5-hydroxylmethylcytosine. However, the molecular mechanism that regulates this biological process is not clear. Here, we show the evidence that PGC7 (also known as Dppa3 or Stella) interacts with TET2 and TET3 both in vitro and in vivo to suppress the enzymatic activity of TET2 and TET3. Moreover, lacking PGC7 induces the loss of DNA methylation at imprinting loci. Genome-wide analysis of PGC7 reveals a consensus DNA motif that is recognized by PGC7. The CpG islands surrounding the PGC7-binding motifs are hypermethylated. Taken together, our study demonstrates a molecular mechanism by which PGC7 protects DNA methylation from TET family enzyme-dependent oxidation. Oxford University Press 2014-03 2013-12-09 /pmc/articles/PMC3950671/ /pubmed/24322296 http://dx.doi.org/10.1093/nar/gkt1261 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), 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 Bian, Chunjing
Yu, Xiaochun
PGC7 suppresses TET3 for protecting DNA methylation
title PGC7 suppresses TET3 for protecting DNA methylation
title_full PGC7 suppresses TET3 for protecting DNA methylation
title_fullStr PGC7 suppresses TET3 for protecting DNA methylation
title_full_unstemmed PGC7 suppresses TET3 for protecting DNA methylation
title_short PGC7 suppresses TET3 for protecting DNA methylation
title_sort pgc7 suppresses tet3 for protecting dna methylation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950671/
https://www.ncbi.nlm.nih.gov/pubmed/24322296
http://dx.doi.org/10.1093/nar/gkt1261
work_keys_str_mv AT bianchunjing pgc7suppressestet3forprotectingdnamethylation
AT yuxiaochun pgc7suppressestet3forprotectingdnamethylation