Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation.

Crosses between natural populations of two species of deer mice, Peromyscus maniculatus (BW), and P. polionotus (PO), produce parent-of-origin effects on growth and development. BW females mated to PO males (bwxpo) produce growth-retarded but otherwise healthy offspring. In contrast, PO females mate...

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Main Authors: Christopher D Wiley, Harry H Matundan, Amanda R Duselis, Alison T Isaacs, Paul B Vrana
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2570336?pdf=render
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spelling doaj-13bad2d3cce8440690b39c2c9c9bd52c2020-11-25T01:01:52ZengPublic Library of Science (PLoS)PLoS ONE1932-62032008-01-01310e357210.1371/journal.pone.0003572Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation.Christopher D WileyHarry H MatundanAmanda R DuselisAlison T IsaacsPaul B VranaCrosses between natural populations of two species of deer mice, Peromyscus maniculatus (BW), and P. polionotus (PO), produce parent-of-origin effects on growth and development. BW females mated to PO males (bwxpo) produce growth-retarded but otherwise healthy offspring. In contrast, PO females mated to BW males (POxBW) produce overgrown and severely defective offspring. The hybrid phenotypes are pronounced in the placenta and include POxBW conceptuses which lack embryonic structures. Evidence to date links variation in control of genomic imprinting with the hybrid defects, particularly in the POxBW offspring. Establishment of genomic imprinting is typically mediated by gametic DNA methylation at sites known as gDMRs. However, imprinted gene clusters vary in their regulation by gDMR sequences.Here we further assess imprinted gene expression and DNA methylation at different cluster types in order to discern patterns. These data reveal POxBW misexpression at the Kcnq1ot1 and Peg3 clusters, both of which lose ICR methylation in placental tissues. In contrast, some embryonic transcripts (Peg10, Kcnq1ot1) reactivated the silenced allele with little or no loss of DNA methylation. Hybrid brains also display different patterns of imprinting perturbations. Several cluster pairs thought to use analogous regulatory mechanisms are differentially affected in the hybrids.These data reinforce the hypothesis that placental and somatic gene regulation differs significantly, as does that between imprinted gene clusters and between species. That such epigenetic regulatory variation exists in recently diverged species suggests a role in reproductive isolation, and that this variation is likely to be adaptive.http://europepmc.org/articles/PMC2570336?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Christopher D Wiley
Harry H Matundan
Amanda R Duselis
Alison T Isaacs
Paul B Vrana
spellingShingle Christopher D Wiley
Harry H Matundan
Amanda R Duselis
Alison T Isaacs
Paul B Vrana
Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation.
PLoS ONE
author_facet Christopher D Wiley
Harry H Matundan
Amanda R Duselis
Alison T Isaacs
Paul B Vrana
author_sort Christopher D Wiley
title Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation.
title_short Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation.
title_full Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation.
title_fullStr Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation.
title_full_unstemmed Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation.
title_sort patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2008-01-01
description Crosses between natural populations of two species of deer mice, Peromyscus maniculatus (BW), and P. polionotus (PO), produce parent-of-origin effects on growth and development. BW females mated to PO males (bwxpo) produce growth-retarded but otherwise healthy offspring. In contrast, PO females mated to BW males (POxBW) produce overgrown and severely defective offspring. The hybrid phenotypes are pronounced in the placenta and include POxBW conceptuses which lack embryonic structures. Evidence to date links variation in control of genomic imprinting with the hybrid defects, particularly in the POxBW offspring. Establishment of genomic imprinting is typically mediated by gametic DNA methylation at sites known as gDMRs. However, imprinted gene clusters vary in their regulation by gDMR sequences.Here we further assess imprinted gene expression and DNA methylation at different cluster types in order to discern patterns. These data reveal POxBW misexpression at the Kcnq1ot1 and Peg3 clusters, both of which lose ICR methylation in placental tissues. In contrast, some embryonic transcripts (Peg10, Kcnq1ot1) reactivated the silenced allele with little or no loss of DNA methylation. Hybrid brains also display different patterns of imprinting perturbations. Several cluster pairs thought to use analogous regulatory mechanisms are differentially affected in the hybrids.These data reinforce the hypothesis that placental and somatic gene regulation differs significantly, as does that between imprinted gene clusters and between species. That such epigenetic regulatory variation exists in recently diverged species suggests a role in reproductive isolation, and that this variation is likely to be adaptive.
url http://europepmc.org/articles/PMC2570336?pdf=render
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