{"title":"Fragaria × ananassa幼苗中时钟相关基因和昼夜节律的全基因组鉴定","authors":"Misaki Ishibashi , Norihito Nakamichi , Yuki Hayashida , Haruka Kazumori , Shungo Otagaki , Shogo Matsumoto , Akira Oikawa , Katsuhiro Shiratake","doi":"10.1016/j.plgene.2024.100470","DOIUrl":null,"url":null,"abstract":"<div><div>Flowering time in plants is regulated by a photoperiod-responsive mechanism. Some plant species use a circadian clock-based control mechanism to adapt to variable environments. Strawberry is a horticultural crop that responds to certain photoperiods and temperatures to induce flowering. However, clock-associated genes in octoploid cultivated strawberry (<em>Fragaria × ananassa</em>) have not been defined, and their regulatory mechanism for responding to photoperiods is unclear. We herein targeted 12 clock-associated genes reported in other plant species and performed a genome-wide analysis and expression comparison in <em>F. × ananassa</em> seedlings. Seventy-eight sequences were selected from the <em>F. × ananassa</em> genome. The major domains and <em>cis</em>-acting elements were conserved in each sequence. Transcripts were clearly expressed under continuous light conditions in <em>F. × ananassa</em> seedlings (‘Yotsuboshi’) acclimated to long days. Among them, 9 genes maintained their unique autonomous circadian rhythms and may function as clock genes. LHY (LATE ELONGATED HYPOCOTYL) had the Myb domain and <em>LHY</em> expression peaked in the dawn. PRR (PSEUDO-RESPONSE REGULATOR) family members (<em>PRR9</em>, <em>PRR7</em>, <em>PRR5</em>, and <em>TOC1</em> (<em>TIMING OF CAB EXPRESSION 1</em>)) had a pseudo-receiver domain and CCT domain, and peak expression times began sequentially from the afternoon for <em>PRR9</em> to the evening for <em>TOC1</em>. LUX (LUXARRHYTHMO) had a Myb domain, and <em>LUX</em> expression peaked in evening with <em>ELF3</em> (<em>EARLY FLOWERING 3</em>). FKF1 (<em>FLAVIN-BINDING KELCH REPEAT F BOX 1</em>) had PAS and F-box domains, and <em>FKF1</em> expression peaked in the afternoon. <em>GI</em> (<em>GIGANTEA</em>) expression also peaked in the afternoon. <em>F.</em> × <em>ananassa</em> (‘Yotsuboshi’) appears to have multiple feedback loops comprising clock-associated genes. Although the rhythmic expression of <em>CHE</em> (<em>CCA1 HIKING EXPEDITION</em>) and <em>ZTL</em> (<em>ZEITLUPE</em>) was not observed, they had conserved domains, CHE with the TCP domain and ZTL with the PAS and F-box domains. The present results provide basic information on the circadian clock for the control of <em>F.</em> × <em>ananassa</em> flowering.</div></div>","PeriodicalId":38041,"journal":{"name":"Plant Gene","volume":"40 ","pages":"Article 100470"},"PeriodicalIF":2.2000,"publicationDate":"2024-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genome-wide identification of clock-associated genes and circadian rhythms in Fragaria × ananassa seedlings\",\"authors\":\"Misaki Ishibashi , Norihito Nakamichi , Yuki Hayashida , Haruka Kazumori , Shungo Otagaki , Shogo Matsumoto , Akira Oikawa , Katsuhiro Shiratake\",\"doi\":\"10.1016/j.plgene.2024.100470\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Flowering time in plants is regulated by a photoperiod-responsive mechanism. Some plant species use a circadian clock-based control mechanism to adapt to variable environments. Strawberry is a horticultural crop that responds to certain photoperiods and temperatures to induce flowering. However, clock-associated genes in octoploid cultivated strawberry (<em>Fragaria × ananassa</em>) have not been defined, and their regulatory mechanism for responding to photoperiods is unclear. We herein targeted 12 clock-associated genes reported in other plant species and performed a genome-wide analysis and expression comparison in <em>F. × ananassa</em> seedlings. Seventy-eight sequences were selected from the <em>F. × ananassa</em> genome. The major domains and <em>cis</em>-acting elements were conserved in each sequence. Transcripts were clearly expressed under continuous light conditions in <em>F. × ananassa</em> seedlings (‘Yotsuboshi’) acclimated to long days. Among them, 9 genes maintained their unique autonomous circadian rhythms and may function as clock genes. LHY (LATE ELONGATED HYPOCOTYL) had the Myb domain and <em>LHY</em> expression peaked in the dawn. PRR (PSEUDO-RESPONSE REGULATOR) family members (<em>PRR9</em>, <em>PRR7</em>, <em>PRR5</em>, and <em>TOC1</em> (<em>TIMING OF CAB EXPRESSION 1</em>)) had a pseudo-receiver domain and CCT domain, and peak expression times began sequentially from the afternoon for <em>PRR9</em> to the evening for <em>TOC1</em>. LUX (LUXARRHYTHMO) had a Myb domain, and <em>LUX</em> expression peaked in evening with <em>ELF3</em> (<em>EARLY FLOWERING 3</em>). FKF1 (<em>FLAVIN-BINDING KELCH REPEAT F BOX 1</em>) had PAS and F-box domains, and <em>FKF1</em> expression peaked in the afternoon. <em>GI</em> (<em>GIGANTEA</em>) expression also peaked in the afternoon. <em>F.</em> × <em>ananassa</em> (‘Yotsuboshi’) appears to have multiple feedback loops comprising clock-associated genes. Although the rhythmic expression of <em>CHE</em> (<em>CCA1 HIKING EXPEDITION</em>) and <em>ZTL</em> (<em>ZEITLUPE</em>) was not observed, they had conserved domains, CHE with the TCP domain and ZTL with the PAS and F-box domains. The present results provide basic information on the circadian clock for the control of <em>F.</em> × <em>ananassa</em> flowering.</div></div>\",\"PeriodicalId\":38041,\"journal\":{\"name\":\"Plant Gene\",\"volume\":\"40 \",\"pages\":\"Article 100470\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2024-09-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Gene\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2352407324000258\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Gene","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2352407324000258","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
摘要
植物的开花时间由光周期响应机制调节。一些植物物种利用基于昼夜节律钟的控制机制来适应多变的环境。草莓是一种园艺作物,它能对特定的光周期和温度做出反应,从而诱导开花。然而,八倍体栽培草莓(Fragaria × ananassa)中的时钟相关基因尚未确定,它们对光周期响应的调控机制也不清楚。在此,我们以其他植物物种中报道的 12 个时钟相关基因为目标,对 F. × ananassa 幼苗进行了全基因组分析和表达比较。从 F. × ananassa 基因组中筛选出 78 个序列。每个序列的主要结构域和顺式作用元件都是保守的。在适应长日照的 F. × ananassa幼苗('Yotsuboshi')中,转录本在连续光照条件下明显表达。其中,9 个基因保持了独特的自主昼夜节律,可能具有时钟基因的功能。LHY(LATE ELONGATED HYPOCOTYL)具有Myb结构域,LHY的表达在黎明达到峰值。PRR(PSEUDO-RESPONSE REGULATOR)家族成员(PRR9、PRR7、PRR5 和 TOC1(TIMING OF CAB EXPRESSION 1))具有伪接收结构域和 CCT 结构域,其表达峰值从 PRR9 的下午到 TOC1 的傍晚依次出现。LUX(LUXARRHYTHMO)有一个 Myb 结构域,LUX 的表达峰值与 ELF3(EARLY FLOWERING 3)一起出现在傍晚。FKF1(FLAVIN-BINDING KELCH REPEAT F BOX 1)具有 PAS 和 F-box 结构域,FKF1 的表达在下午达到峰值。GI(GIGANTEA)的表达也在下午达到峰值。F. × ananassa('Yotsuboshi')似乎有多个由时钟相关基因组成的反馈回路。虽然没有观察到 CHE(CCA1 HIKING EXPEDITION)和 ZTL(ZEITLUPE)的节律性表达,但它们具有保守的结构域,CHE 具有 TCP 结构域,ZTL 具有 PAS 和 F-box 结构域。本研究结果为控制 F. × ananassa 开花的昼夜节律时钟提供了基本信息。
Genome-wide identification of clock-associated genes and circadian rhythms in Fragaria × ananassa seedlings
Flowering time in plants is regulated by a photoperiod-responsive mechanism. Some plant species use a circadian clock-based control mechanism to adapt to variable environments. Strawberry is a horticultural crop that responds to certain photoperiods and temperatures to induce flowering. However, clock-associated genes in octoploid cultivated strawberry (Fragaria × ananassa) have not been defined, and their regulatory mechanism for responding to photoperiods is unclear. We herein targeted 12 clock-associated genes reported in other plant species and performed a genome-wide analysis and expression comparison in F. × ananassa seedlings. Seventy-eight sequences were selected from the F. × ananassa genome. The major domains and cis-acting elements were conserved in each sequence. Transcripts were clearly expressed under continuous light conditions in F. × ananassa seedlings (‘Yotsuboshi’) acclimated to long days. Among them, 9 genes maintained their unique autonomous circadian rhythms and may function as clock genes. LHY (LATE ELONGATED HYPOCOTYL) had the Myb domain and LHY expression peaked in the dawn. PRR (PSEUDO-RESPONSE REGULATOR) family members (PRR9, PRR7, PRR5, and TOC1 (TIMING OF CAB EXPRESSION 1)) had a pseudo-receiver domain and CCT domain, and peak expression times began sequentially from the afternoon for PRR9 to the evening for TOC1. LUX (LUXARRHYTHMO) had a Myb domain, and LUX expression peaked in evening with ELF3 (EARLY FLOWERING 3). FKF1 (FLAVIN-BINDING KELCH REPEAT F BOX 1) had PAS and F-box domains, and FKF1 expression peaked in the afternoon. GI (GIGANTEA) expression also peaked in the afternoon. F. × ananassa (‘Yotsuboshi’) appears to have multiple feedback loops comprising clock-associated genes. Although the rhythmic expression of CHE (CCA1 HIKING EXPEDITION) and ZTL (ZEITLUPE) was not observed, they had conserved domains, CHE with the TCP domain and ZTL with the PAS and F-box domains. The present results provide basic information on the circadian clock for the control of F. × ananassa flowering.
Plant GeneAgricultural and Biological Sciences-Plant Science
CiteScore
4.50
自引率
0.00%
发文量
42
审稿时长
51 days
期刊介绍:
Plant Gene publishes papers that focus on the regulation, expression, function and evolution of genes in plants, algae and other photosynthesizing organisms (e.g., cyanobacteria), and plant-associated microorganisms. Plant Gene strives to be a diverse plant journal and topics in multiple fields will be considered for publication. Although not limited to the following, some general topics include: Gene discovery and characterization, Gene regulation in response to environmental stress (e.g., salinity, drought, etc.), Genetic effects of transposable elements, Genetic control of secondary metabolic pathways and metabolic enzymes. Herbal Medicine - regulation and medicinal properties of plant products, Plant hormonal signaling, Plant evolutionary genetics, molecular evolution, population genetics, and phylogenetics, Profiling of plant gene expression and genetic variation, Plant-microbe interactions (e.g., influence of endophytes on gene expression; horizontal gene transfer studies; etc.), Agricultural genetics - biotechnology and crop improvement.