{"title":"SCL15 Regulates the Release of Seed Dormancy in Arabidopsis thaliana by Integrating the Circadian Clock, Hormonal Signals and Cell Wall Remodelling.","authors":"Ming-Jun Gao, Qi Chen, Cathy Coutu, Fuyou Fu, Bianyun Yu, Xiang Li, Z Jeffrey Chen, Dwayne Hegedus","doi":"10.1111/ppl.70467","DOIUrl":null,"url":null,"abstract":"<p><p>Dormancy release and germination of the seed are two separate, but continuous phases controlled by both external (e.g., light and temperature) and internal (e.g., circadian clock and hormones) cues. In eudicot seeds, the endosperm tissues play a key role in dormancy release and germination through dynamic modulation of wall components and biomechanics. However, the mode of action by which the circadian oscillator influences dormancy release by modulation of endosperm wall biomechanics remains elusive. SCARECROW-LIKE15 (SCL15) represses embryonic gene expression in seedlings through interaction with HISTONE DEACETYLASE19 (HDA19) in Arabidopsis thaliana. Here, we report that SCL15 plays a positive role in primary dormancy release, which is associated with gene expression changes in circadian, abscisic acid, auxin and cell wall (CW) remodelling pathways, based on studies using SCL15 mutant and Napin promoter-driven SCL15 expression lines. SCL15 was found to affect the expression of genes whose products modify endosperm wall biomechanical features, possibly through regulation of local auxin accumulation and evening-phased clock components. RNA-seq analysis supported the notion that dormancy release is associated with changes in the expression of genes associated with circadian and hormone-mediated pathways, which in turn affect CW structure.</p>","PeriodicalId":20164,"journal":{"name":"Physiologia plantarum","volume":"177 5","pages":"e70467"},"PeriodicalIF":3.6000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12415678/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiologia plantarum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/ppl.70467","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
Dormancy release and germination of the seed are two separate, but continuous phases controlled by both external (e.g., light and temperature) and internal (e.g., circadian clock and hormones) cues. In eudicot seeds, the endosperm tissues play a key role in dormancy release and germination through dynamic modulation of wall components and biomechanics. However, the mode of action by which the circadian oscillator influences dormancy release by modulation of endosperm wall biomechanics remains elusive. SCARECROW-LIKE15 (SCL15) represses embryonic gene expression in seedlings through interaction with HISTONE DEACETYLASE19 (HDA19) in Arabidopsis thaliana. Here, we report that SCL15 plays a positive role in primary dormancy release, which is associated with gene expression changes in circadian, abscisic acid, auxin and cell wall (CW) remodelling pathways, based on studies using SCL15 mutant and Napin promoter-driven SCL15 expression lines. SCL15 was found to affect the expression of genes whose products modify endosperm wall biomechanical features, possibly through regulation of local auxin accumulation and evening-phased clock components. RNA-seq analysis supported the notion that dormancy release is associated with changes in the expression of genes associated with circadian and hormone-mediated pathways, which in turn affect CW structure.
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.