Evidence map›Paper›PMID 42771260›Full record

ArticlePlant cell reports2026

Homoeologous exchange-associated ABA catabolism rewiring contributes to salinity tolerance in a synthetic tetraploid rice.

Bingqi Zhang, Tiantian Zhu, Guo Li, Shu Ma, Di An, Changyin Cui, Yingying Tan, Chunming Xu, Ying Wu, Bao Liu

Abstract read
PubMed Publisher
In one paragraph

Article in Plant cell reports, 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

10 authors.

Bingqi Zhang *Key Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun, 130024, China.
Tiantian Zhu *Key Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun, 130024, China.
Guo LiKey Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun, 130024, China.
Shu MaKey Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun, 130024, China.
Di AnKey Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun, 130024, China.
Changyin CuiKey Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun, 130024, China.
Yingying TanKey Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun, 130024, China.
Chunming XuKey Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun, 130024, China.
Ying WuKey Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun, 130024, China. wuy003@nenu.edu.cn.
Bao LiuKey Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun, 130024, China. baoliu@nenu.edu.cn.

Funding

Fundamental Research Funds for the Central Universities 2412025QG003Jilin Provincial Key Research and Development Plan Project 20240303002NCNational Natural Science Foundation of China 32441058
6 · The paper itself

Abstract

key messageAltered ABA-related regulation is associated with transgressive salinity tolerance in a synthetic tetraploid rice carrying extensive post-polyploidy homoeologous exchanges. Plant polyploids often show higher environment resilience than their congeneric diploid progenitors. However, it remains unclear whether these traits arise directly from whole-genome duplication (WGD) or evolve through post-WGD changes. Here, we show that transgressive salt tolerance occurs in ca. 1.71% of an early-generation synthetic rice tetraploid from japonica-indica subspecies hybridization. Genome resequencing unravels extensive homoeologous exchanges (HEs) but without genomic features distinguishing the tolerant vs. sensitive plants. In contrast, RNA-seq-based transcriptome-profiling enables distinct separation of the tolerant and sensitive plants. A KEGG pathway analysis indicates that the downregulated genes in tolerant plants are enriched in the abscisic acid (ABA)-degradation pathway. Expression and coding-sequence analyses identified the ABA catabolic gene OsABA8ox3 as a candidate associated with the salt-tolerant phenotype. Endogenous ABA measurements and exogenous ABA and Na

Indexed as

Abscisic AcidOryzaSalt ToleranceTetraploidyGene Expression ProfilingGene Expression Regulation, PlantPlant ProteinsAbscisic AcidPlant ProteinsAbscisic acid metabolismHomoeolog-specific expressionJaponica–indica segmental allotetraploidOryza sativaSalt stressTranscriptome profiling

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.