4.5 Article

Tracking age-correlated DNA methylation markers in the young

期刊

FORENSIC SCIENCE INTERNATIONAL-GENETICS
卷 36, 期 -, 页码 50-59

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.fsigen.2018.06.011

关键词

DNA methylation; Children; Adolescents; Individual age; Illumina; EpiTYPER (R); Age estimation

资金

  1. CHRONOGEN [BIO2013-42188-R]
  2. Ministry of Economy and Competitiveness, Spain
  3. ERDF funds
  4. Xunta de Galicia, Spain, as part of the Plan Galego de Investigacion, Innovacion e Crecemento 2011-2015, Axudas de apoio a etapa de formacion post-doutoral, Plan I2C
  5. training subprogam by the Ministry of Economy and Competitiveness, Spain (as part of the Plan Estatal de Investigacion Cientifica y Tecnica y de Innovacion) [201320]
  6. ISCIII-SGEFI / FEDER [PT13/0001]
  7. BioBank IBSP-CV [PT13/0010/0064]

向作者/读者索取更多资源

DNA methylation is the most extensively studied epigenetic signature, with a large number of studies reporting age-correlated CpG sites in overlapping genes. However, most of these studies lack sample coverage of individuals under 18 years old and therefore little is known about the progression of DNA methylation patterns in children and adolescents. In the present study we aimed to select candidate age-correlated DNA methylation markers based on public datasets from Illumina BeadChip arrays and previous publications, then to explore the resulting markers in 209 blood samples from donors aged between 2 to 18 years old using the EpiTYPER (R) DNA methylation analysis system. Results from our analyses identified six genes highly correlated with age in the young, in particular the gene KCNAB3, which indicates its potential as a highly informative and specific age biomarker for childhood and adolescence. We outline a preliminary age prediction model based on quantile regression that uses data from the six CpG sites most strongly correlated with age ranges extended to include children and adolescents.

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