| Literature DB >> 24615936 |
Hiroshi Kobayashi1, Yumi Higashiura2, Natsuki Koike2, Juria Akasaka2, Chiharu Uekuri2, Kana Iwai2, Emiko Niiro2, Sachiko Morioka2, Yuki Yamada2.
Abstract
There is now accumulating evidence that endometriosis is a disease associated with an epigenetic disorder. Genomic imprinting is an epigenetic phenomenon known to regulate DNA methylation of either maternal or paternal alleles. We hypothesize that hypermethylated endometriosis-associated genes may be enriched at imprinted gene loci. We sought to determine whether downregulated genes associated with endometriosis susceptibility are associated with chromosomal location of the known paternally and maternally expressed imprinting genes. Gene information has been gathered from National Center for Biotechnology Information database geneimprint.com. Several researchers have identified specific loci with strong DNA methylation in eutopic endometrium and ectopic lesion with endometriosis. Of the 29 hypermethylated genes in endometriosis, 19 genes were located near 45 known imprinted foci. There may be an association of the genomic location between genes specifically downregulated in endometriosis and epigenetically imprinted genes.Entities:
Keywords: chromosomal location; endometriosis; hypermethylation; imprinting genes
Year: 2014 PMID: 24615936 PMCID: PMC4126219 DOI: 10.1177/1933719114526473
Source DB: PubMed Journal: Reprod Sci ISSN: 1933-7191 Impact factor: 3.060