Compromised stability of DNA methylation and transposon immobilization in mosaic <i>Arabidopsis</i> epigenomes

Jon Reinders(University of Geneva), Brande B. H. Wulff(Instituto de Biología Molecular y Celular de Plantas), Marie Mirouze(University of Geneva), Arturo Marí‐Ordóñez(Instituto de Biología Molecular y Celular de Plantas), Mélanie Dapp(University of Geneva), Wilfried Rozhon(University of Vienna), Etienne Bucher(University of Geneva), Grégory Theiler(University of Geneva), Jerzy Paszkowski(University of Geneva)
Genes & Development
April 15, 2009
Cited by 435Open Access
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Abstract

Transgenerational epigenetic inheritance has been defined by the study of relatively few loci. We examined a population of recombinant inbred lines with epigenetically mosaic chromosomes consisting of wild-type and CG methylation-depleted segments (epiRILs). Surprisingly, transposons that were immobile in the parental lines displayed stochastic movement in 28% of the epiRILs. Although analysis after eight generations of inbreeding, supported by genome-wide DNA methylation profiling, identified recombined parental chromosomal segments, these were interspersed with unexpectedly high frequencies of nonparental methylation polymorphism. Hence, epigenetic inheritance in hybrids derived from parents with divergent epigenomes permits long-lasting epi-allelic interactions that violate Mendelian expectations. Such persistently "unstable" epigenetic states complicate linkage-based epigenomic mapping. Thus, future epigenomic analyses should consider possible genetic instabilities and alternative mapping strategies.


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