中国农业科学 ›› 2025, Vol. 58 ›› Issue (18): 3728-3743.doi: 10.3864/j.issn.0578-1752.2025.18.011

• 园艺 • 上一篇    下一篇

芦笋过氧化物还原酶(Peroxiredoxins)基因家族全基因组鉴定及表达分析

仪泽会(), 王颖, 宋慧霞, 赵婧, 毛丽萍   

  1. 山西农业大学园艺学院/蔬菜花卉种质资源创新与利用山西省重点实验室,太原 030031
  • 收稿日期:2025-04-25 接受日期:2025-06-19 出版日期:2025-09-18 发布日期:2025-09-18
  • 联系方式: 仪泽会,E-mail:yizehui2008bj@163.com
  • 基金资助:
    山西省重点实验室开放基金课题(SCHHZDSYS2024-13); 山西省高校科技创新项目(2022L104); 山西农业大学农业科技创新研究课题(YCX2020YQ07)

Genome-Wide Identification and Expression Analysis of Peroxiredoxins Gene Family in Asparagus officinalis

YI ZeHui(), WANG Ying, SONG HuiXia, ZHAO Jing, MAO LiPing   

  1. College of Horticulture, Shanxi Agricultural University/Shanxi Key Laboratory of Germplasm Resources Innovation and Utilization of Vegetable and Flower, Taiyuan 030031
  • Received:2025-04-25 Accepted:2025-06-19 Published:2025-09-18 Online:2025-09-18

摘要:

【目的】在全基因组范围内对芦笋过氧化物还原酶(Peroxiredoxins)基因家族进行鉴定,分析其组织表达特征及其对逆境胁迫、休眠及休眠解除的响应,为后续AoPrxs的功能研究及育种应用奠定基础。【方法】以芦笋基因组数据为材料,采用生物信息学方法鉴定芦笋Prx家族成员,并利用ProtParam、Cell-PLoc2.0、SWISS-MODEL和MEME等工具获取理化性质、亚细胞定位、基因结构及保守基序等信息。基于RNA-Seq数据和实时荧光定量PCR(qRT-PCR)方法,分析AoPrxs的组织表达特征及对逆境胁迫、休眠及休眠解除的应答。【结果】芦笋Prx家族含有AoPrx1AoPrx6共6个成员,其蛋白均含有保守的PXXXTXXC序列,氨基酸序列长度为162—268 aa,蛋白分子量为17 397.96—29 246.45 Da。从AoPrx1AoPrx6中共鉴定出220(38种)个顺式作用元件,涉及植物生长发育、激素响应、胁迫响应和光响应。共线性分析显示,芦笋Prx与小麦Prx和水稻Prx的同源性更高。系统进化分析将6个AoPrxs划分为5个亚家族,每个亚家族内部成员的基因结构、氨基酸序列和蛋白质结构均高度保守。值得注意的是,AoPrx1和AoPrx2不含“分解”Cys残基,但其与PrxⅡB亚家族成员的氨基酸序列和蛋白质结构的相似性远高于1-Cys亚家族成员。因此,将其分类为PrxⅠB。组织表达分析表明,AoPrx2在所有组织中均高度表达,而AoPrx5则仅在超雄花的雄蕊中高度表达。逆境胁迫分析显示,盐碱胁迫可显著诱导芦笋幼苗根系中AoPrx5的表达;盐、干旱及弱光处理可显著提高芦笋茎叶组织中AoPrx4的表达量,而拟茎点霉菌侵染则正相反。此外,AoPrx2AoPrx4AoPrx5还可能在芦笋的休眠与休眠解除中发挥作用。【结论】从芦笋基因组中鉴定到6个Prx家族成员,分布于5条染色体,均包含保守的PXXXTXXC序列,并被划分为5个亚家族。家族成员具有不同的表达模式。其中,AoPrx5与芦笋雄蕊的生长发育及根系耐盐性密切相关;AoPrx4在对盐、干旱、弱光及拟茎点霉菌胁迫响应中发挥重要作用;而AoPrx2AoPrx4AoPrx5则参与了芦笋的休眠与休眠解除。

关键词: 芦笋, Prx基因家族, 全基因组鉴定, 生物信息学, 表达分析

Abstract:

【Objective】The peroxiredoxin (Prx) gene family in garden asparagus was systematically identified at the genome-wide level. The tissue-specific expression profiles and responses to abiotic stress, dormancy, and dormancy release were comprehensively investigated, providing a critical foundation for further functional characterization and breeding applications of AoPrxs. 【Method】Using the genomic data of asparagus, the members of the Prx family were identified through bioinformatics methods. The physicochemical properties, subcellular localization, gene structures, and conserved motifs of the AoPrxs were predicted using ProtParam, Cell-PLoc 2.0, SWISS-MODEL, and MEME tools, respectively. The tissue-specific expression patterns of AoPrxs and their responses to diverse stresses, dormancy, and dormancy release were systematically analyzed using RNA-Seq data and real-time fluorescent quantitative PCR (qRT-PCR). 【Result】The AoPrx family contains six members, designated AoPrx1-AoPrx6, all of which contain the conserved PXXXTXXC sequence. Their amino acid sequences ranged from 162 to 268 residues, with molecular weights ranging from 17 397.96 to 29 246.45 Da. A total of 220 (38 types) cis-acting elements were identified in AoPrxs, including those involved in plant growth and development, stress response, hormone signaling, and light response. Collinearity analysis revealed that AoPrx has a higher homology with TaPrx and OsPrx. Phylogenetic analysis classified the AoPrxs into five subfamilies, each exhibiting highly conserved gene structures, amino acid sequences, and protein structures. Notably, AoPrx1 and AoPrx2 lack the ‘resolving’ Cys residue but exhibit greater similarity in both amino acid sequence and protein structure to members of the PrxⅡB subfamily than to those of the 1-Cys subfamily. Consequently, they were classified into the PrxⅠB subfamily. Tissue expression analysis showed that AoPrx2 is ubiquitously expressed across all tissues, in contrast to AoPrx5, which showed stamen-specific upregulation in supermale flowers. The expression profile under adverse stress conditions indicated that salt-alkali stress significantly upregulated AoPrx5 expression in the roots of asparagus seedlings. Additionally, salt, drought, and low-light treatments markedly enhanced AoPrx4 expression levels in the stems and leaves of asparagus seedlings, while infection by Phomopsis asparagi exerted an opposite regulatory effect on AoPrx4 expression. Furthermore, AoPrx2, AoPrx4, and AoPrx5 may also be involved in the regulatory processes of dormancy induction and release in asparagus. 【Conclusion】Six Prx family members were identified in the asparagus genome, distributed across five chromosomes. All members contained the conserved PXXXTXXC motif and were phylogenetically classified into five subfamilies. Expression profiling revealed subfunctionalization among Prx paralogs: AoPrx5 was closely associated with stamen development and root salt tolerance. AoPrx4 played a pivotal role in the responses of stem and leaf tissues to salt, drought, low-light conditions, and phomopsis asparagi stress. Moreover, AoPrx2, AoPrx4, and AoPrx5 were also involved in the regulation of asparagus dormancy induction and release.

Key words: Asparagus officinalis L., Prx gene family, genome-wide identification, bioinformatics, expression analysis