Back to Search Start Over

Passive and active DNA methylation and the interplay with genetic variation in gene regulation

Authors :
Thomas Giger
Corinne Gehrig
Periklis Makrythanasis
Halit Ongen
Luciana Romano
Deborah Bielser
Audrey Letourneau
Tuuli Lappalainen
Christelle Borel
Stephen B. Montgomery
Julien Bryois
Emilie Falconnet
Stylianos E. Antonarakis
Alfonso Buil
Michel Guipponi
Maria Gutierrez-Arcelus
Alisa Yurovsky
Maryline Gagnebin
Alexandra Planchon
Ismael Padioleau
Emmanouil T. Dermitzakis
Source :
eLife, Vol 2 (2013), Genome Biology, eLife, Vol. 2 (2013) P. e00523
Publication Year :
2013
Publisher :
eLife Sciences Publications, Ltd, 2013.

Abstract

Variations occur throughout our genome. These variations can cause genes to be expressed (switched on) in slightly different ways among individuals. Moreover, the same gene can also be expressed in different ways in different cells within an individual. A third level of variation is supplied by epigenetic markers: these are molecules that bind to the DNA at specific points and can have profound effects on the expression of nearby genes. One such epigenetic marker is the addition of a methyl group to a cytosine base, a process that is known as DNA methylation. DNA methylation usually happens when a cytosine base is next to a guanine base, forming a CpG site. In mammals, most CpG sites have methyl groups attached, although regions with a lot of CpG sites (called CpG islands) are mostly unmethylated. Initial studies suggested that methylation prevented particular genes from being expressed, but more recent work has indicated that methylation can be associated with both reduced and increased expression of genes. Moreover, it is not clear if this association is active (i.e., changes in methylation drive changes in gene expression) or passive (DNA methylation is the result of gene regulation). Now, Gutierrez-Arcelus et al. have carried out a large-scale study to clarify the relationships between three different types of gene-related variations among individuals. They extracted fibroblasts, T-cells and lymphoblastoid cells from the umbilical cords of 204 babies, and analysed them for variations in DNA sequence, gene expression and DNA methylation. Their results show that the associations between the three are more complex than was previously thought. Gutierrez-Arcelus et al. show that the mechanisms that control the association between the variations in DNA methylation and gene expression in individuals are likely to be different to those that are responsible for the establishment of methylation patterns during the process of cell differentiation. They also find that the association between DNA methylation and gene expression can be either active or passive, and can depend on the context in which they occur in our genome. Finally, where the two copies or alleles of a gene are not equally expressed in a given cell, the difference in expression is primarily regulated by DNA sequence variation, with DNA methylation having little or no role on its own. Equally complex interactions and effects are expected in further studies of genetic and epigenetic variation.

Details

ISSN :
2050084X
Volume :
2
Database :
OpenAIRE
Journal :
eLife
Accession number :
edsair.doi.dedup.....08df811ea14825fe2fd1e1d8e55fb45c
Full Text :
https://doi.org/10.7554/elife.00523