Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions.

Genomic imprinting is the phenomena that leads to silencing of one copy of a gene inherited from a specific parent. Mutations in imprinted regions have been involved in diseases showing parent of origin effects. Identifying genes with evidence of parent of origin expression patterns in family studie...

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Main Authors: Sahar V Mozaffari, Michelle M Stein, Kevin M Magnaye, Dan L Nicolae, Carole Ober
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0203906
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spelling doaj-b1b2a836876d403f8a85f9fe0f0467632021-03-03T19:45:36ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01139e020390610.1371/journal.pone.0203906Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions.Sahar V MozaffariMichelle M SteinKevin M MagnayeDan L NicolaeCarole OberGenomic imprinting is the phenomena that leads to silencing of one copy of a gene inherited from a specific parent. Mutations in imprinted regions have been involved in diseases showing parent of origin effects. Identifying genes with evidence of parent of origin expression patterns in family studies allows the detection of more subtle imprinting. Here, we use allele specific expression in lymphoblastoid cell lines from 306 Hutterites related in a single pedigree to provide formal evidence for parent of origin effects. We take advantage of phased genotype data to assign parent of origin to RNA-seq reads in individuals with gene expression data. Our approach identified known imprinted genes, two putative novel imprinted genes, PXDC1 and PWAR6, and 14 genes with asymmetrical parent of origin gene expression. We used gene expression in peripheral blood leukocytes (PBL) to validate our findings, and then confirmed imprinting control regions (ICRs) using DNA methylation levels in the PBLs.https://doi.org/10.1371/journal.pone.0203906
collection DOAJ
language English
format Article
sources DOAJ
author Sahar V Mozaffari
Michelle M Stein
Kevin M Magnaye
Dan L Nicolae
Carole Ober
spellingShingle Sahar V Mozaffari
Michelle M Stein
Kevin M Magnaye
Dan L Nicolae
Carole Ober
Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions.
PLoS ONE
author_facet Sahar V Mozaffari
Michelle M Stein
Kevin M Magnaye
Dan L Nicolae
Carole Ober
author_sort Sahar V Mozaffari
title Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions.
title_short Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions.
title_full Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions.
title_fullStr Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions.
title_full_unstemmed Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions.
title_sort parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Genomic imprinting is the phenomena that leads to silencing of one copy of a gene inherited from a specific parent. Mutations in imprinted regions have been involved in diseases showing parent of origin effects. Identifying genes with evidence of parent of origin expression patterns in family studies allows the detection of more subtle imprinting. Here, we use allele specific expression in lymphoblastoid cell lines from 306 Hutterites related in a single pedigree to provide formal evidence for parent of origin effects. We take advantage of phased genotype data to assign parent of origin to RNA-seq reads in individuals with gene expression data. Our approach identified known imprinted genes, two putative novel imprinted genes, PXDC1 and PWAR6, and 14 genes with asymmetrical parent of origin gene expression. We used gene expression in peripheral blood leukocytes (PBL) to validate our findings, and then confirmed imprinting control regions (ICRs) using DNA methylation levels in the PBLs.
url https://doi.org/10.1371/journal.pone.0203906
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