{"title":"Natural regulatory variations of MdIAA14b links auxin signalling to fruit cell density and firmness in apple","authors":"Hussain Ahmed, Zhiyong Wu, Md Marufur Rahman, Zhe Zhou, Yarong Wang, Chunyan Wang, Zhenli Yan, Qiming Gao, Zhenzhen Liu, Yaru Zhang, Xiangpeng Meng, Yiru Yang, Xiuhua Gao, Tianyu Wu, Hengtao Zhang, Jia-Long Yao","doi":"10.1016/j.plaphy.2026.111852","DOIUrl":null,"url":null,"abstract":"<div><div>Fruit firmness is a major determinant of apple quality and shelf life. It is known to be regulated by ethylene signalling, however, the function of auxin in it is not known. Here, we identified <em>MdIAA14b</em>, an auxin-responsive gene, as a key regulator of apple fruit firmness. <em>MdIAA14b</em> showed allele-specific expression (ASE) across multiple apple cultivars and developmental stages as revealed by RNA-seq analysis. Relative to the low expression allele, the promoter of the high expression allele contained two insertions of 9 bp and 1636 bp. The 9-bp insertion generated an ARF-binding site that enabled activation by the transcription factor <em>MdARF1</em>. The 1636-bp insert, identified as a transposable element (TE), disrupted and reduced the expression of a long non-coding RNA (<em>lncRNA_iaa14b</em>), which exhibited an inverse expression pattern relative to <em>MdIAA14b.</em> Apple cultivars homozygous for the high-expression allele displayed increased cell density, smaller cell size, and firmer fruit, whereas those homozygous for the low-expression allele had larger cells and softer fruit. <em>MdIAA14b</em> overexpression in tomato increased cell number and enhanced fruit firmness. Furthermore, <em>MdIAA14b</em> overexpression altered the expression of auxin-responsive genes, including members of ARF, SAUR, and GH3 families, which may relate to increased cell division. Together, these findings reveal that naturally occurring cis-regulatory variations control <em>MdIAA14b</em> expression and, consequently, apple fruit firmness. This work provides a molecular framework for improving fruit texture and highlights the role of cis-regulatory variation in allele-specific gene regulation in perennial fruit crops.</div></div>","PeriodicalId":20234,"journal":{"name":"Plant Physiology and Biochemistry","volume":"239 ","pages":"Article 111852"},"PeriodicalIF":6.2000,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology and Biochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0981942826008387","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/10/13 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Fruit firmness is a major determinant of apple quality and shelf life. It is known to be regulated by ethylene signalling, however, the function of auxin in it is not known. Here, we identified MdIAA14b, an auxin-responsive gene, as a key regulator of apple fruit firmness. MdIAA14b showed allele-specific expression (ASE) across multiple apple cultivars and developmental stages as revealed by RNA-seq analysis. Relative to the low expression allele, the promoter of the high expression allele contained two insertions of 9 bp and 1636 bp. The 9-bp insertion generated an ARF-binding site that enabled activation by the transcription factor MdARF1. The 1636-bp insert, identified as a transposable element (TE), disrupted and reduced the expression of a long non-coding RNA (lncRNA_iaa14b), which exhibited an inverse expression pattern relative to MdIAA14b. Apple cultivars homozygous for the high-expression allele displayed increased cell density, smaller cell size, and firmer fruit, whereas those homozygous for the low-expression allele had larger cells and softer fruit. MdIAA14b overexpression in tomato increased cell number and enhanced fruit firmness. Furthermore, MdIAA14b overexpression altered the expression of auxin-responsive genes, including members of ARF, SAUR, and GH3 families, which may relate to increased cell division. Together, these findings reveal that naturally occurring cis-regulatory variations control MdIAA14b expression and, consequently, apple fruit firmness. This work provides a molecular framework for improving fruit texture and highlights the role of cis-regulatory variation in allele-specific gene regulation in perennial fruit crops.
期刊介绍:
Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement.
Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB.
Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.