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A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro
BACKGROUND: CpG dinucleotide-rich genomic DNA regions, known as CpG islands (CGIs), can be methylated at their cytosine residues as an epigenetic mark that is stably inherited during cell mitosis. Differentially methylated regions (DMRs) are genomic regions showing different degrees of DNA methylati...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008136/ https://www.ncbi.nlm.nih.gov/pubmed/24106769 http://dx.doi.org/10.1186/1471-2164-14-692 |
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author | Cocozza, Sergio Scala, Giovanni Miele, Gennaro Castaldo, Imma Monticelli, Antonella |
author_facet | Cocozza, Sergio Scala, Giovanni Miele, Gennaro Castaldo, Imma Monticelli, Antonella |
author_sort | Cocozza, Sergio |
collection | PubMed |
description | BACKGROUND: CpG dinucleotide-rich genomic DNA regions, known as CpG islands (CGIs), can be methylated at their cytosine residues as an epigenetic mark that is stably inherited during cell mitosis. Differentially methylated regions (DMRs) are genomic regions showing different degrees of DNA methylation in multiple samples. In this study, we focused our attention on CGIs showing different DNA methylation between two culture replicas of the same cell line. RESULTS: We used methylation data of 35 cell lines from the Encyclopedia of DNA Elements (ENCODE) consortium to identify CpG islands that were differentially methylated between replicas of the same cell line and denoted them Inter Replicas Differentially Methylated CpG islands (IRDM-CGIs). We identified a group of IRDM-CGIs that was consistently shared by different cell lines, and denoted it common IRDM-CGIs. X chromosome CGIs were overrepresented among common IRDM-CGIs. Autosomal IRDM-CGIs were preferentially located in gene bodies and intergenic regions had a lower G + C content, a smaller mean length, and a reduced CpG percentage. Functional analysis of the genes associated with autosomal IRDM-CGIs showed that many of them are involved in DNA binding and development. CONCLUSIONS: Our results show that several specific functional and structural features characterize common IRDM-CGIs. They may represent a specific subset of CGIs that are more prone to being differentially methylated for their intrinsic characteristics. |
format | Online Article Text |
id | pubmed-4008136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40081362014-05-19 A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro Cocozza, Sergio Scala, Giovanni Miele, Gennaro Castaldo, Imma Monticelli, Antonella BMC Genomics Research Article BACKGROUND: CpG dinucleotide-rich genomic DNA regions, known as CpG islands (CGIs), can be methylated at their cytosine residues as an epigenetic mark that is stably inherited during cell mitosis. Differentially methylated regions (DMRs) are genomic regions showing different degrees of DNA methylation in multiple samples. In this study, we focused our attention on CGIs showing different DNA methylation between two culture replicas of the same cell line. RESULTS: We used methylation data of 35 cell lines from the Encyclopedia of DNA Elements (ENCODE) consortium to identify CpG islands that were differentially methylated between replicas of the same cell line and denoted them Inter Replicas Differentially Methylated CpG islands (IRDM-CGIs). We identified a group of IRDM-CGIs that was consistently shared by different cell lines, and denoted it common IRDM-CGIs. X chromosome CGIs were overrepresented among common IRDM-CGIs. Autosomal IRDM-CGIs were preferentially located in gene bodies and intergenic regions had a lower G + C content, a smaller mean length, and a reduced CpG percentage. Functional analysis of the genes associated with autosomal IRDM-CGIs showed that many of them are involved in DNA binding and development. CONCLUSIONS: Our results show that several specific functional and structural features characterize common IRDM-CGIs. They may represent a specific subset of CGIs that are more prone to being differentially methylated for their intrinsic characteristics. BioMed Central 2013-10-10 /pmc/articles/PMC4008136/ /pubmed/24106769 http://dx.doi.org/10.1186/1471-2164-14-692 Text en Copyright © 2013 Cocozza et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Cocozza, Sergio Scala, Giovanni Miele, Gennaro Castaldo, Imma Monticelli, Antonella A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro |
title | A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro |
title_full | A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro |
title_fullStr | A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro |
title_full_unstemmed | A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro |
title_short | A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro |
title_sort | distinct group of cpg islands shows differential dna methylation between replicas of the same cell line in vitro |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008136/ https://www.ncbi.nlm.nih.gov/pubmed/24106769 http://dx.doi.org/10.1186/1471-2164-14-692 |
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