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    枸杞 SnRK基因家族鉴定及表达分析

    Identification and expression analysis of SnRK gene family in Lycium barbarum

    • 摘要:
      目的 SnRK蛋白激酶家族在植物生长发育和逆境响应中发挥重要作用。本研究旨在鉴定并分析枸杞SnRK基因家族,为揭示其在果实发育中的功能机制提供理论依据。
      方法 采用NCBI、SMART、Pfam、Protparam tool、MEME、PlantCare、Mega等软件进行生物信息学分析,鉴定枸杞基因组中的LbSnRK基因家族,分析其蛋白理化性质、基因结构、保守基序、启动子顺式作用元件及系统进化关系,并结合转录组数据分析其在枸杞果实发育过程中的表达模式。
      结果 (1)从枸杞基因组中鉴定出49个LbSnRK基因,LbSnRK基因家族分为LbSnRK1(3个成员)、LbSnRK2(16个成员)和LbSnRK3(30个成员)3个亚家族;(2)启动子顺式作用元件分析显示,LbSnRKs基因富含GT1-motif(生长素响应)、G-box(茉莉酸信号)、ABRE(ABA响应)等元件,可参与激素介导的生长发育与逆境响应通路;共线性分析表明,片段复制是LbSnRK基因家族扩增的主要机制,13对重复基因对的Ka/Ks 值均小于1,表明其进化过程中受纯化选择。(3)转录组分析发现,LbSnRK1.1、LbSnRK2.3/2.4/2.7/2.10及多个LbSnRK3成员在果实发育过程中显著表达。
      结论 LbSnRK基因家族在枸杞果实发育过程中具有潜在调控作用,研究结果将为后续解析SnRK家族基因调控果实发育的分子机制提供核心靶点,为枸杞果实品质改良的分子育种工作提供重要基因资源。

       

      Abstract:
      Objective Lycium barbarum is an important medicinal herb. Sucrose non-fermenting 1 (SNF1)-related protein kinase (SnRK) family plays important functions in plant growth and development. This paper aims to identify and analyze the SnRK gene family in L. barbarum, providing a theoretical basis for revealing its functional mechanisms during fruit development.
      Method Bioinformatics analysis was performed using software including NCBI, SMART, Pfam, Protparam tool, MEME, PlantCare, and Mega to identify the LbSnRK gene family in L. barbarum genome. The study analyzed the physicochemical properties of its proteins, gene structures, conserved motifs, promoter cis-acting elements, and phylogenetic relationships. Transcriptome data were integrated to examine its expression patterns during Lycium barbarum fruit development.
      Result (1) Forty-nine LbSnRK genes were identified from the L. barbarum genome, with the LbSnRK gene family being divided into three subfamilies: LbSnRK1 (3 members), LbSnRK2 (16 members), and LbSnRK3 (30 members). Chromosomal localization analysis revealed that all 49 LbSnRKs genes were distributed across 12 chromosomes of L. barbarum. Among these, chromosomes 1 and 2 harbored the highest number of LbSnRKs members, each containing five members. (2) Analysis of promoter cis-acting elements revealed that LbSnRK genes were rich in motifs, such as GT1 (auxin response), G-box (jasmonic acid signaling), and ABRE (ABA response), suggesting involvement in hormone-mediated growth and development as well as stress response pathways. Co-linearity analysis indicated that segmental duplication was the primary mechanism for LbSnRK gene family expansion. The Ka/Ks ratios of all 13 duplicate gene pairs were less than 1, suggesting they had undergone purifying selection during evolution. (3) Transcriptome analysis revealed that LbSnRK1.1, LbSnRK2.3/2.4/2.7/2.10, and multiple LbSnRK3 members were significantly expressed during fruit development.
      Conclusion The LbSnRK gene family exhibits potential regulatory roles in L. barbarum fruit development, providing core targets for elucidating the molecular mechanisms, by which these genes regulate fruit development. It also offers crucial genetic resources and theoretical support for molecular breeding efforts, aiming at improving L. barbarum fruit quality.

       

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