Evidence map›Paper›PMID 40985693›Full record

ArticlePlant physiology2025

Genome assembly and DNA methylation variation in an epimutant population of hybrid poplar clone NL895.

Jie He, Guang-Zheng Diao, Yang-Fan Feng, Hao-Ran Liao, Ying Guo, Li-Na Mei, Fang-Fang Fu, Tongming Yin, Fuliang Cao, Liang-Jiao Xue

Abstract read
In one paragraph

Article in Plant physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Jie HeState Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Tree Genetics and Biotechnology of Educational Department of China, Key Laboratory of Tree Genetics and Silvicultural Sciences of Jiangsu Province, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037, China.
Guang-Zheng DiaoState Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Tree Genetics and Biotechnology of Educational Department of China, Key Laboratory of Tree Genetics and Silvicultural Sciences of Jiangsu Province, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037, China.
Yang-Fan FengState Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Tree Genetics and Biotechnology of Educational Department of China, Key Laboratory of Tree Genetics and Silvicultural Sciences of Jiangsu Province, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037, China.
Hao-Ran LiaoState Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Tree Genetics and Biotechnology of Educational Department of China, Key Laboratory of Tree Genetics and Silvicultural Sciences of Jiangsu Province, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037, China.
Ying GuoState Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Tree Genetics and Biotechnology of Educational Department of China, Key Laboratory of Tree Genetics and Silvicultural Sciences of Jiangsu Province, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037, China.
Li-Na MeiState Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Tree Genetics and Biotechnology of Educational Department of China, Key Laboratory of Tree Genetics and Silvicultural Sciences of Jiangsu Province, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037, China.
Fang-Fang FuState Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Tree Genetics and Biotechnology of Educational Department of China, Key Laboratory of Tree Genetics and Silvicultural Sciences of Jiangsu Province, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037, China.ORCID 0000-0002-3187-9308
Tongming YinState Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Tree Genetics and Biotechnology of Educational Department of China, Key Laboratory of Tree Genetics and Silvicultural Sciences of Jiangsu Province, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037, China.
Fuliang CaoState Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Tree Genetics and Biotechnology of Educational Department of China, Key Laboratory of Tree Genetics and Silvicultural Sciences of Jiangsu Province, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037, China.
Liang-Jiao XueState Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Tree Genetics and Biotechnology of Educational Department of China, Key Laboratory of Tree Genetics and Silvicultural Sciences of Jiangsu Province, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037, China.ORCID 0000-0003-1766-5298

Funding

Biological Breeding-National Science and Technology 2023ZD0405601National Natural Science Foundation of China 32171826Natural Science Foundation of Jiangsu Province BK20220411
6 · The paper itself

Abstract

Epimutant populations represent important genetic resources for plant breeding and selection. However, the variation and dynamics of epigenomic modifications among epimutants are still elusive. In this study, we analyzed DNA methylation patterns at both whole-genome and allelic levels in an epimutant population of a model hybrid poplar NL895 (Populus deltoides × Populus euramericana cv. "Nanlin895"). Epimutants were generated through the application of 5-Azacytidine (5-Aza) during tissue culture. A haplotype-resolved assembly of NL895 was constructed to serve as a reference for epigenomic analysis. Compared to control plants, averaged DNA methylation levels across the entire genome were reduced in epimutants. The methylation patterns of epimutants exhibited high diversity in several aspects, including the number of differentially methylated regions (DMRs), distribution of DMRs in sequence contexts, and genomic features. The observed epigenomic diversity suggests stochastic effects resulting from 5-Aza treatment. At the gene level, non-expressed genes consistently displayed higher rates of methylation across all examined epimutants. Among allele-specific expressed genes (ASEGs), fold changes between parental alleles were more pronounced in allele pairs exhibiting greater disparities in DNA methylation rates. For allele-specific methylation regions (ASMRs), the differences in methylation levels were notably elevated in ASMRs overlapped with genomic structural variations (SVs). Our results provide valuable germplasm resources characterized by phenotypic variations for poplar breeding, and the dynamics of DNA methylation in hybrid poplar epimutants highlights potential clues for application of hybrid vigor.

Indexed as

DNA MethylationEpigenesis, GeneticGenome, PlantPopulusAllelesGene Expression Regulation, PlantGenetic VariationMutation

Identifiers

PMID40985693
PMCPMC12501979

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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.