Epigenome-wide inheritance of cytosine methylation variants in a recombinant inbred population

Cytosine DNA methylation is one avenue for passing information through cell divisions. Here, we present epigenomic analyses of soybean recombinant inbred lines (RILs) and their parents. Identification of differentially methylated regions (DMRs) revealed that DMRs mostly cosegregated with the genotyp...

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Published in:Genome research Vol. 23; no. 10; pp. 1663 - 1674
Main Authors: Schmitz, Robert J, He, Yupeng, Valdés-López, Oswaldo, Khan, Saad M, Joshi, Trupti, Urich, Mark A, Nery, Joseph R, Diers, Brian, Xu, Dong, Stacey, Gary, Ecker, Joseph R
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Language:English
Published: United States Cold Spring Harbor Laboratory Press 01-10-2013
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Abstract Cytosine DNA methylation is one avenue for passing information through cell divisions. Here, we present epigenomic analyses of soybean recombinant inbred lines (RILs) and their parents. Identification of differentially methylated regions (DMRs) revealed that DMRs mostly cosegregated with the genotype from which they were derived, but examples of the uncoupling of genotype and epigenotype were identified. Linkage mapping of methylation states assessed from whole-genome bisulfite sequencing of 83 RILs uncovered widespread evidence for local methylQTL. This epigenomics approach provides a comprehensive study of the patterns and heritability of methylation variants in a complex genetic population over multiple generations, paving the way for understanding how methylation variants contribute to phenotypic variation.
AbstractList Cytosine DNA methylation is one avenue for passing information through cell divisions. Here, we present epigenomic analyses of soybean recombinant inbred lines (RILs) and their parents. Identification of differentially methylated regions (DMRs) revealed that DMRs mostly cosegregated with the genotype from which they were derived, but examples of the uncoupling of genotype and epigenotype were identified. Linkage mapping of methylation states assessed from whole-genome bisulfite sequencing of 83 RILs uncovered widespread evidence for local methylQTL. This epigenomics approach provides a comprehensive study of the patterns and heritability of methylation variants in a complex genetic population over multiple generations, paving the way for understanding how methylation variants contribute to phenotypic variation.
Author Nery, Joseph R
Schmitz, Robert J
Joshi, Trupti
Urich, Mark A
Valdés-López, Oswaldo
Stacey, Gary
He, Yupeng
Xu, Dong
Ecker, Joseph R
Khan, Saad M
Diers, Brian
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FG02-02ER15309
USDOE Office of Science (SC), Biological and Environmental Research (BER). Biological Systems Science Division
These authors contributed equally to this work.
Present address: Laboratorio de Bioquímica, Facultad de Estudios Superiores Iztacala, Universidad Nacional Autónoma de México, Tlalnepantla, Estado De México, Mexico 54090.
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Snippet Cytosine DNA methylation is one avenue for passing information through cell divisions. Here, we present epigenomic analyses of soybean recombinant inbred lines...
SourceID pubmedcentral
osti
proquest
crossref
pubmed
SourceType Open Access Repository
Aggregation Database
Index Database
StartPage 1663
SubjectTerms Arabidopsis - genetics
Arabidopsis - metabolism
BASIC BIOLOGICAL SCIENCES
Biochemistry & Molecular Biology
Biotechnology & Applied Microbiology
Bisulfite
Cell Division
Chromosome Mapping
Cytosine - metabolism
DNA Methylation
DNA Transposable Elements
DNA, Plant - genetics
DNA, Plant - metabolism
DNA, Recombinant
Epigenesis, Genetic
Epigenomics
Gene Expression Regulation, Plant
Genes, Plant
Genetic Variation
Genetics & Heredity
Genome, Plant
Genotype
Glycine max - genetics
Glycine max - metabolism
Inbreeding
Polymorphism, Single Nucleotide
Quantitative Trait Loci
Sequence Analysis
Title Epigenome-wide inheritance of cytosine methylation variants in a recombinant inbred population
URI https://www.ncbi.nlm.nih.gov/pubmed/23739894
https://search.proquest.com/docview/1443381861
https://search.proquest.com/docview/1458529608
https://www.osti.gov/servlets/purl/1625624
https://pubmed.ncbi.nlm.nih.gov/PMC3787263
Volume 23
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