期刊论文详细信息
BMC Genomics
A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro
Research Article
Imma Castaldo1  Giovanni Scala2  Gennaro Miele2  Sergio Cocozza3  Antonella Monticelli4 
[1] Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli “Federico II”, Naples, Italy;Gruppo Interdipartimentale di Bioinformatica e Biologia Computazionale, Università di Napoli “Federico II”, Naples, Italy;Dipartimento di Fisica, Università degli Studi di Napoli “Federico II”, Naples, Italy;Istituto Nazionale di Fisica Nucleare, Sezione di Napoli, Naples, Italy;Gruppo Interdipartimentale di Bioinformatica e Biologia Computazionale, Università di Napoli “Federico II”, Naples, Italy;Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli “Federico II”, Naples, Italy;Gruppo Interdipartimentale di Bioinformatica e Biologia Computazionale, Università di Napoli “Federico II”, Naples, Italy;Istituto di Endocrinologia ed Oncologia Sperimentale (IEOS), CNR, Naples, Italy;
关键词: CpG Islands;    Methylation;    Differentially methylated regions;    Epigenetics;   
DOI  :  10.1186/1471-2164-14-692
 received in 2013-05-27, accepted in 2013-10-05,  发布年份 2013
来源: Springer
PDF
【 摘 要 】

BackgroundCpG 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.ResultsWe 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.ConclusionsOur 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.

【 授权许可】

Unknown   
© Cocozza et al.; licensee BioMed Central Ltd. 2013. This article is published under license to BioMed Central Ltd. 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.

【 预 览 】
附件列表
Files Size Format View
RO202311096599313ZK.pdf 371KB PDF download
【 参考文献 】
  • [1]
  • [2]
  • [3]
  • [4]
  • [5]
  • [6]
  • [7]
  • [8]
  • [9]
  • [10]
  • [11]
  • [12]
  • [13]
  • [14]
  • [15]
  • [16]
  • [17]
  • [18]
  • [19]
  • [20]
  • [21]
  • [22]
  • [23]
  • [24]
  • [25]
  • [26]
  • [27]
  • [28]
  • [29]
  • [30]
  • [31]
  • [32]
  • [33]
  • [34]
  • [35]
  文献评价指标  
  下载次数:0次 浏览次数:0次