Hongyan Cai , Zhengwen Lv , Jun Zeng , Nenghui Li , Hang Li , Chen Wang , Huaqiang Tan
{"title":"强光胁迫对毛缕凤蝶生理和转录组的影响","authors":"Hongyan Cai , Zhengwen Lv , Jun Zeng , Nenghui Li , Hang Li , Chen Wang , Huaqiang Tan","doi":"10.1016/j.plaphy.2025.109900","DOIUrl":null,"url":null,"abstract":"<div><div><em>Pterocladiella capillacea</em>, a subtropical red alga rich in bioactive compounds, holds significant pharmaceutical value and is widely distributed in intertidal and subtidal rocky reefs. However, the natural biomass of this species declines due to climate change and anthropogenic activities, posing challenges to its aquaculture and commercial exploitation. High-light stress represents a critical environmental factor affecting its growth and reproduction, yet the underlying molecular mechanisms remain poorly understood. This study investigates the effects of high-light stress on chlorophyll fluorescence parameters, physiological indices, and transcriptomic profiles of <em>P. capillacea</em> collected from Naozhou Island, Zhanjiang. Results reveal that high-light stress significantly perturbs chlorophyll fluorescence parameters, photosynthetic rates, photosynthetic pigment biosynthesis, malondialdehyde content, antioxidant enzyme activities, and osmolyte accumulation. The transcriptomic analysis identifies 2,281, 7,640, and 8800 differentially expressed genes (DEGs) under 120 μmol m<sup>−2</sup>s<sup>−1</sup>, 300 μmol m<sup>−2</sup>s<sup>−1</sup>, and 500 μmol m<sup>−2</sup>s<sup>−1</sup> treatments, respectively. Functional enrichment analysis (GO and KEGG) highlighted DEGs primarily involved in photosynthesis, antioxidant systems, sucrose/starch metabolism, and chlorophyll biosynthesis. Temporal expression pattern analysis further uncovered five distinct gene expression trends associated with increasing light intensity. These findings provide novel insights into the physiological and molecular mechanisms underlying high-light tolerance in <em>P. capillacea</em>, offering a theoretical foundation for future molecular breeding programs to improve stress resilience in this economically important alga.</div></div>","PeriodicalId":20234,"journal":{"name":"Plant Physiology and Biochemistry","volume":"224 ","pages":"Article 109900"},"PeriodicalIF":6.1000,"publicationDate":"2025-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The impact of high-light stress on the physiology and transcriptome of Pterocladiella capillacea\",\"authors\":\"Hongyan Cai , Zhengwen Lv , Jun Zeng , Nenghui Li , Hang Li , Chen Wang , Huaqiang Tan\",\"doi\":\"10.1016/j.plaphy.2025.109900\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><em>Pterocladiella capillacea</em>, a subtropical red alga rich in bioactive compounds, holds significant pharmaceutical value and is widely distributed in intertidal and subtidal rocky reefs. However, the natural biomass of this species declines due to climate change and anthropogenic activities, posing challenges to its aquaculture and commercial exploitation. High-light stress represents a critical environmental factor affecting its growth and reproduction, yet the underlying molecular mechanisms remain poorly understood. This study investigates the effects of high-light stress on chlorophyll fluorescence parameters, physiological indices, and transcriptomic profiles of <em>P. capillacea</em> collected from Naozhou Island, Zhanjiang. Results reveal that high-light stress significantly perturbs chlorophyll fluorescence parameters, photosynthetic rates, photosynthetic pigment biosynthesis, malondialdehyde content, antioxidant enzyme activities, and osmolyte accumulation. The transcriptomic analysis identifies 2,281, 7,640, and 8800 differentially expressed genes (DEGs) under 120 μmol m<sup>−2</sup>s<sup>−1</sup>, 300 μmol m<sup>−2</sup>s<sup>−1</sup>, and 500 μmol m<sup>−2</sup>s<sup>−1</sup> treatments, respectively. Functional enrichment analysis (GO and KEGG) highlighted DEGs primarily involved in photosynthesis, antioxidant systems, sucrose/starch metabolism, and chlorophyll biosynthesis. Temporal expression pattern analysis further uncovered five distinct gene expression trends associated with increasing light intensity. These findings provide novel insights into the physiological and molecular mechanisms underlying high-light tolerance in <em>P. capillacea</em>, offering a theoretical foundation for future molecular breeding programs to improve stress resilience in this economically important alga.</div></div>\",\"PeriodicalId\":20234,\"journal\":{\"name\":\"Plant Physiology and Biochemistry\",\"volume\":\"224 \",\"pages\":\"Article 109900\"},\"PeriodicalIF\":6.1000,\"publicationDate\":\"2025-04-10\",\"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/S0981942825004280\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology and Biochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0981942825004280","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
The impact of high-light stress on the physiology and transcriptome of Pterocladiella capillacea
Pterocladiella capillacea, a subtropical red alga rich in bioactive compounds, holds significant pharmaceutical value and is widely distributed in intertidal and subtidal rocky reefs. However, the natural biomass of this species declines due to climate change and anthropogenic activities, posing challenges to its aquaculture and commercial exploitation. High-light stress represents a critical environmental factor affecting its growth and reproduction, yet the underlying molecular mechanisms remain poorly understood. This study investigates the effects of high-light stress on chlorophyll fluorescence parameters, physiological indices, and transcriptomic profiles of P. capillacea collected from Naozhou Island, Zhanjiang. Results reveal that high-light stress significantly perturbs chlorophyll fluorescence parameters, photosynthetic rates, photosynthetic pigment biosynthesis, malondialdehyde content, antioxidant enzyme activities, and osmolyte accumulation. The transcriptomic analysis identifies 2,281, 7,640, and 8800 differentially expressed genes (DEGs) under 120 μmol m−2s−1, 300 μmol m−2s−1, and 500 μmol m−2s−1 treatments, respectively. Functional enrichment analysis (GO and KEGG) highlighted DEGs primarily involved in photosynthesis, antioxidant systems, sucrose/starch metabolism, and chlorophyll biosynthesis. Temporal expression pattern analysis further uncovered five distinct gene expression trends associated with increasing light intensity. These findings provide novel insights into the physiological and molecular mechanisms underlying high-light tolerance in P. capillacea, offering a theoretical foundation for future molecular breeding programs to improve stress resilience in this economically important alga.
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.