Abstract

BackgroundEpigenetic modifications play important roles in plant and animal development. DNA methylation impacts the transposable element (TE) silencing, gene imprinting and expression regulation.ResultsThrough a genome-wide analysis, DNA methylation peaks were characterized and mapped in maize embryo and endosperm genome, respectively. Distinct methylation level was observed across maize embryo and endosperm. The maize embryo genome contained more DNA methylation than endosperm. Totally, 985,478 CG islands (CGIs) were identified and most of them were unmethylated. More CGI shores were methylated than CGIs in maize suggested that DNA methylation level was not positively correlated with CpG density. The promoter sequence and transcriptional termination region (TTR) were more methylated than the gene body (intron and exon) region based on peak number and methylated depth. Result showed that 99% TEs were methylated in maize embryo, but a large portion of them (34.8%) were not methylated in endosperm. Maize embryo and endosperm exhibit distinct pattern/level of methylation. The most differentially methylated region between embryo and endosperm are CGI shores. Our results indicated that DNA methylation is associated with both gene silencing and gene activation in maize. Many genes involved in embryogenesis and seed development were found differentially methylated in embryo and endosperm. We found 41.5% imprinting genes were similarly methylated and 58.5% imprinting genes were differentially methylated between embryo and endosperm. Methylation level was associated with allelic silencing of only a small number of imprinting genes. The expression of maize DEMETER-like (DME-like) gene and MBD101 gene (MBD4 homolog) were higher in endosperm than in embryo. These two genes may be associated with distinct methylation levels across maize embryo and endosperm.ConclusionsThrough MeDIP-seq we systematically analyzed the methylomes of maize embryo and endosperm and results indicated that the global methylation status of embryo was more than that of the endosperm. Differences could be observed at the total number of methylation peaks, DMRs and specific methylated genes which were tightly associated with development of embryo and endosperm. Our results also revealed that many DNA methylation regions didn’t affect transcription of the corresponding genes.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-014-1204-7) contains supplementary material, which is available to authorized users.

Highlights

  • Epigenetic modifications play important roles in plant and animal development

  • Methylomic profiling of embryo and endosperm in maize We generated a total of 2,748,497,900 bp of DNA immunoprecipitation sequencing (MeDIP-seq) data from maize endosperm and 2,807,090,100 bp data from maize embryo

  • Our results showed that 58.5% imprinting genes were differentially methylated between embryo and endosperm

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Summary

Introduction

DNA methylation impacts the transposable element (TE) silencing, gene imprinting and expression regulation. DNA methylation, a conserved epigenetic mechanism involved in many important biological processes, is associated with gene silencing, X chromosome inactivation in females, and maintenance of genomic integrity in eukaryotes [1,2,3]. DNA methylation in plant genomes predominantly occurs at CpG site. This is maintained by METHYLTRANSFERASE1 (MET1), a homolog of DNA methyltransferase (Dnmt). Plants DNA methylation occurs at CpHpG and CpHpH sites, and is maintained by CHROMOMETHYLASE3 (CMT3) [7,8,9]. The methylated cytosine contexts in animals and plants are different, DNA methylation is conserved in both TEs and genes. More methylation was detected in exons to compare with TEs regions [12,13,14]

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