Evidence map›Paper›PMID 24131563›Full record

ArticleGenome research2014

Genome-wide high resolution parental-specific DNA and histone methylation maps uncover patterns of imprinting regulation in maize.

Mei Zhang, Shaojun Xie, Xiaomei Dong, Xin Zhao, Biao Zeng, Jian Chen, Hui Li, Weilong Yang, Hainan Zhao, Gaokui Wang and 5 more

Abstract read
In one paragraph

Article in Genome research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

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0cells of the map it votes in
92citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

92 citing papers in PubMed.

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  11. Using targeted genome methylation for crop improvement.Journal of experimental botany · 2025
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32 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

15 authors.

Mei ZhangState Key Laboratory of Agrobiotechnology and National Maize Improvement Center, Department of Plant Genetics and Breeding, China Agricultural University, Beijing 100193, China.
Shaojun Xie
Xiaomei Dong
Xin Zhao
Biao Zeng
Jian Chen
Hui Li
Weilong Yang
Hainan Zhao
Gaokui Wang
Zongliang Chen
Silong Sun
Andrew Hauck
Weiwei Jin
Jinsheng Lai

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic imprinting is a specific epigenetic phenomenon in which a subset of genes is expressed depending on their parent-of-origin. Two types of chromatin modifications, DNA methylation and histone modification, are generally believed to be involved in the regulation of imprinting. However, the genome-wide correlation between allele-specific chromatin modifications and imprinted gene expression in maize remains elusive. Here we report genome-wide high resolution allele-specific maps of DNA methylation and histone H3 lysine 27 trimethylation (H3K27me3) in maize endosperm. For DNA methylation, thousands of parent-of-origin dependent differentially methylated regions (pDMRs) were identified. All pDMRs were uniformly paternally hypermethylated and maternally hypomethylated. We also identified 1131 allele-specific H3K27me3 peaks that are preferentially present in the maternal alleles. Maternally expressed imprinted genes (MEGs) and paternally expressed imprinted genes (PEGs) had different patterns of allele-specific DNA methylation and H3K27me3. Allele-specific expression of MEGs was not directly related to allele-specific H3K27me3, and only a subset of MEGs was associated with maternal-specific DNA demethylation, which was primarily located in the upstream and 5' portion of gene body regions. In contrast, allele-specific expression of a majority of PEGs was related to maternal-specific H3K27me3, with a subgroup of PEGs also associated with maternal-specific DNA demethylation. Both pDMRs and maternal H3K27me3 peaks associated with PEGs are enriched in gene body regions. Our results indicate highly complex patterns of regulation on genetic imprinting in maize endosperm.

Indexed as

AllelesDNA, PlantEndospermEpigenesis, GeneticGene Expression ProfilingGene Expression Regulation, PlantGenes, PlantGenome, PlantGenomic ImprintingHistonesMethylationPlant ProteinsZea maysDNA, PlantHistonesPlant Proteins

Identifiers

PMID24131563
PMCPMC3875858

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.