Evidence map›Paper›PMID 41057937›Full record

ArticleGenome biology2025

Pan-S-locus analysis reveals insights into the origin and evolution of self-incompatibility in the orange subfamily.

Jianbing Hu, Zezhen Du, Chenchen Liu, Hao Wen, Cong Liu, Peng Chen, Chunmei Shi, Junli Ye, QianHua Ji, Xiuxin Deng and 4 more

Abstract read
In one paragraph

Article in Genome biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Genome-wide identification and analysis ofFrontiers in plant science · 2026
    Article
  3. Article
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

14 authors.

Jianbing Hu *National Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, P. R. China. hujianbing@mail.hzau.edu.cn.
Zezhen Du *National Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, P. R. China.
Chenchen LiuNational Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, P. R. China.
Hao WenNational Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, P. R. China.
Cong LiuNational Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, P. R. China.
Peng ChenHorticultural Institute, Hunan Academy of Agricultural Sciences, Changsha, 410125, P. R. China.
Chunmei ShiNational Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, P. R. China.
Junli YeNational Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, P. R. China.
QianHua JiFruit Tree Research Institute, Zhaoqing University, Zhaoqing, 526061, P. R. China.
Xiuxin DengNational Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, P. R. China.
Maurice BoschInstitute of Biological, Environmental and Rural Sciences (IBERS), Aberystwyth University, Aberystwyth, UK.
Zongcheng LinNational Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, P. R. China.
Wen-Biao JiaoNational Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, P. R. China. jiao@mail.hzau.edu.cn.
Lijun ChaiNational Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, P. R. China. chailijun@mail.hzau.edu.cn.

Funding

Hubei Provincial Natural Science Foundation of China 2023AFB094National Key Research and Development Program of China 2023YFD1200100National Natural Science Foundation of China 32302489, 32270685Scientific Research Innovation Capability Support Project for Young Faculty ZYGXONJSKYCXNLZCXM-A5The China Agriculture Research System CARS-26The Fundamental Research Funds for the Central Universities of China 2662024YLPY001
6 · The paper itself

Abstract

backgroundSelf-incompatibility is controlled by a highly polymorphic supergene complex, the S-locus, which is structurally complex, rich in repetitive sequences, and varies in length from hundreds of kilobases to tens of megabases across different plant families. Due to these challenges, the S-locus has been fully reconstructed in only a few species, limiting our understanding of its evolutionary dynamics.

resultsThis study systematically explores the evolutionary mechanisms and structural characteristics of the self-incompatibility system mediated by S-RNase in the Aurantioideae (orange subfamily) of Rutaceae. We construct a pan-S-locus framework spanning 11 genera within the orange subfamily from 14 newly assembled genomes from representative accessions and the analysis of 41 published citrus genomes. Our analyses reveal significant structural variations and transposable element (TE)-driven pseudogenization of SLF genes. By constructing a comprehensive library of S-RNases and developing a novel genotyping pipeline, we reveal divergent frequencies of S-RNases between self-incompatible and self-compatible populations. Comparative analyses demonstrate a unique evolutionary trajectory marked by asynchronous core nonS-genes duplication and TE-mediated structural diversification, distinct from other families. Innovatively, we identified TE-induced self-incompatibility loss as the primary driver of self-compatibility transition, which implies the uniqueness of the origin and evolution of self-incompatibility in the orange subfamily.

conclusionsThrough the construction and characterization of the pan-S-locus, this study provides profound insight into the origin and evolution of the S-locus in the orange subfamily. These findings not only advance our understanding of self-incompatibility mechanisms, but also establish a foundational framework for investigating the evolution of the gametophytic self-incompatibility systems in other families.

Indexed as

Evolution, MolecularRibonucleasesSelf-Incompatibility in Flowering PlantsDNA Transposable ElementsGenome, PlantPhylogenyPlant ProteinsDNA Transposable ElementsPlant Proteinsribonuclease SRibonucleasesCitrusEvolutionPan-S-locusSelf-incompatibilityS-RNaseTransposable elements

Identifiers

PMID41057937
PMCPMC12506349

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LicenceCC BY-NC-ND
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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.