Evidence map›Paper›PMID 42801713›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Integration of the D-Genome Reshapes Gene Transcription, Chromatin Architecture, and Metabolome of Allohexaploid Wheat, Leading to Enhanced Environmental Adaptability.

Yanyan Liu, Tao Zhu, Ziru Zhou, Wei Chen, Chao He, Xinkai Zhou, Xin Wang, Chuanye Chen, Bo Yang, Jiaqi Wei and 14 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. 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

24 authors.

Yanyan Liu *National Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Tao Zhu *State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, China.ORCID https://orcid.org/0000-0001-9667-498X
Ziru Zhou *National Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Wei ChenNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.ORCID https://orcid.org/0000-0001-7225-3785
Chao HeNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Xinkai ZhouState Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, China.
Xin WangNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Chuanye ChenNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Bo YangNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Jiaqi WeiNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Caixia LanNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.ORCID https://orcid.org/0000-0001-8436-9486
Mengmeng LiuNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Handong SuNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.ORCID https://orcid.org/0000-0001-8621-2941
Qiang LiNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Xin HuNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Siteng BiNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Weizhi OuyangNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.ORCID https://orcid.org/0000-0003-0099-4044
Xingwang LiNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Hailiang MaoNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Masahiro KishiInternational Maize and Wheat Improvement Center (CIMMYT), Mexico City, Mexico.
Kerstin KaufmannDepartment For Plant Cell and Molecular Biology, Institute For Biology, Humboldt-Universität Zu Berlin, Berlin, Germany.ORCID https://orcid.org/0000-0001-7960-6256
Alisdair R FernieMax Planck Institute of Molecular Plant Physiology, Potsdam, Germany.ORCID https://orcid.org/0000-0001-9000-335X
Dijun ChenState Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, China.ORCID https://orcid.org/0000-0002-7456-2511
Wenhao YanNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.ORCID https://orcid.org/0000-0001-8165-7335

Funding

China Postdoctoral Science Foundation 2019M662665International Science and Technology Cooperation Project of Hubei Province 2023EHA060National Key Laboratory of Crop Genetic Improvement Self-Research Program ZW19A0201National Key Research and Development Program of China 2024YFD1201104National Natural Science Foundation of China 32070656National Natural Science Foundation of China 32202248
6 · The paper itself

Abstract

The hybridization-led integration of the D-genome into domesticated tetraploid wheat gave rise to allohexaploid wheat, the most cultivated wheat globally grown across diverse environmental conditions. However, the regulatory mechanisms by which this genomic integration confers increased environmental adaptability in allohexaploid remains largely unexplored. Here, we investigated the change of transcriptome, chromatin interactome and metabolome in three independent polyploidization events. Our findings reveal that polyploidization triggers the activation of defense-related genes through a comprehensive reorganization of the epigenome and 3D chromatin architecture. Furthermore, polyploidization significantly enriches secondary metabolites-specifically alkaloids and flavonoids-which are pivotal for environmental adaptation. We further found that B-subgenome genes TaRLK-1B and TaRLK-3B are activated via de novo chromatin interactions to enhance alkali stress tolerance, whereas TaGT-2D boosts UV-B resistance through the accumulation of glycosylated flavonoids. These results shed light on the mechanistic basis of enhanced adaptability in hexaploid wheat, especially to salt, alkali, and UV-B stress, and highlight the indispensable contribution of the D-genome to the evolutionary success of the allohexaploid lineage.

Indexed as

3D interactomeadaptabilityepigenomemetabolomepolyploidizaitontranscriptional regulationwheat

Identifiers

PMID42801713
PMCPMC13616400

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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.