Sandra Rios-Carrasco, Emilio García-Caffarel, Yuridia Cruz-Zamora, Edgar Jiménez-Díaz, Felipe Cruz-García
{"title":"S-RNase Internalisation and Vacuolar Targeting via Clathrin-Dependent Endocytosis Mediate Interspecific Pollen Rejection in Nicotiana.","authors":"Sandra Rios-Carrasco, Emilio García-Caffarel, Yuridia Cruz-Zamora, Edgar Jiménez-Díaz, Felipe Cruz-García","doi":"10.1111/ppl.70418","DOIUrl":null,"url":null,"abstract":"<p><p>In Nicotiana, the multiallelic S-locus controls self-incompatibility (SI), which encodes S-RNases in the pollen's pistil and S-locus F-box (SLF) proteins. Their interaction mediates S allele-specific pollen rejection, preventing self-fertilisation. Beyond its role in SI, the S-locus also contributes to unilateral interspecific (UI) incompatibility, where self-incompatible pistils reject pollen from self-compatible species. Experimental evidence indicates that S-RNases alone can mediate UI. In transgenic Nicotiana tabacum-a naturally self-compatible species-expression of the S-RNase is sufficient to trigger self-pollen rejection, demonstrating that S-RNases can function independently of a complete SI system. However, the molecular mechanisms underlying S-RNase-mediated factor-independent UI remain unclear. To explore this, we analysed S-RNase trafficking in N. tabacum, which lacks endogenous S-RNases and SLFs. Pollen tube assays and confocal microscopy showed that S-RNases are internalised via clathrin-mediated endocytosis and transported in vesicles to vacuoles. Disruption of vacuoles releases S-RNases into the cytoplasm, coinciding with RNA degradation. These findings reveal an SLF-independent pathway for S-RNase internalisation, sequestration, and release, supporting that S-RNase compartmentalisation underlies pollen rejection between self-compatible and self-incompatible Nicotiana. This mechanism may be central in evolving interspecific reproductive barriers within the genus.</p>","PeriodicalId":20164,"journal":{"name":"Physiologia plantarum","volume":"177 4","pages":"e70418"},"PeriodicalIF":5.4000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12279473/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiologia plantarum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/ppl.70418","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
In Nicotiana, the multiallelic S-locus controls self-incompatibility (SI), which encodes S-RNases in the pollen's pistil and S-locus F-box (SLF) proteins. Their interaction mediates S allele-specific pollen rejection, preventing self-fertilisation. Beyond its role in SI, the S-locus also contributes to unilateral interspecific (UI) incompatibility, where self-incompatible pistils reject pollen from self-compatible species. Experimental evidence indicates that S-RNases alone can mediate UI. In transgenic Nicotiana tabacum-a naturally self-compatible species-expression of the S-RNase is sufficient to trigger self-pollen rejection, demonstrating that S-RNases can function independently of a complete SI system. However, the molecular mechanisms underlying S-RNase-mediated factor-independent UI remain unclear. To explore this, we analysed S-RNase trafficking in N. tabacum, which lacks endogenous S-RNases and SLFs. Pollen tube assays and confocal microscopy showed that S-RNases are internalised via clathrin-mediated endocytosis and transported in vesicles to vacuoles. Disruption of vacuoles releases S-RNases into the cytoplasm, coinciding with RNA degradation. These findings reveal an SLF-independent pathway for S-RNase internalisation, sequestration, and release, supporting that S-RNase compartmentalisation underlies pollen rejection between self-compatible and self-incompatible Nicotiana. This mechanism may be central in evolving interspecific reproductive barriers within the genus.
期刊介绍:
Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.