生物技术通报 ›› 2026, Vol. 42 ›› Issue (8): 133-141.doi: 10.13560/j.cnki.biotech.bull.1985.2025-1113

• 研究报告 • 上一篇    

糜子伪响应调节蛋白PRR基因家族的鉴定及对光周期的响应

崔秀妍1, 代春阳1, 张谊婷1, 田翔2, 陈凌2, 乔治军2, 王海岗2(), 王君杰2()   

  1. 1.山西农业大学农学院,太谷 030800
    2.山西农业大学农业基因资源研究中心,太原 030031
  • 收稿日期:2025-10-16 出版日期:2026-08-26 发布日期:2026-08-17
  • 通讯作者: 王君杰xiaoleiwangjie@163.com
    王海岗nkywhg@126.com
  • 基金资助:
    中央引导地方科技发展资金项目(YDZJSX20231A035);山西农业大学“科技创新提升工程”项目(CXGC2023095)

Identification of the Pseudo-response Regulator PRR Gene Family in Broomcorn Millet and Its Response to Photoperiod

CUI Xiu-yan1, DAI Chun-yang1, ZHANG Yi-ting1, TIAN Xiang2, CHEN Ling2, QIAO Zhi-jun2, WANG Hai-gang2(), WANG Jun-jie2()   

  1. 1.College of Agronomy, Shanxi Agricultural University, Taigu 030800
    2.Center for Agricultural Genetic Resources Research, Shanxi Agricultural University, Taiyuan 030031
  • Received:2025-10-16 Published:2026-08-26 Online:2026-08-17

摘要:

目的 伪响应调节蛋白(pseudo-response regulators, PRRs)在植物昼夜节律调控与开花期调控中发挥重要作用。基于全基因组水平对糜子(Panicum miliaceum L.)伪应答蛋白基因家族进行系统鉴定,为其生物学功能提供理论依据。 方法 采用生物信息学方法,对糜子PRR基因家族进行理化性质分析、Motif、基因结构分析、共线性分析、系统进化分析,利用实时荧光定量PCR(RT-qPCR)对不同光周期处理下的糜子PRR基因家族成员表达情况进行分析。 结果 从糜子基因组中鉴定到7个PRR基因,分别命名为PmPRR1-PmPRR7,不均匀地分布在5条染色体上;系统进化分析表明,PmPRR基因分布在Group 1-Group 3亚家族中。蛋白质保守基序分析显示,有6个基因均含有Motif1、Motif2和Motif3,表明这6个基因高度保守。启动子顺式作用元件分析显示,PmPRR基因与植物光响应、生长发育、胁迫和激素调控。RT-qPCR结果表明,在不同光周期(短日照8 h、中日照14 h、长日照16 h)处理下,PmPRR基因表达水平均存在显著差异。 结论 鉴定出7个PmPRR基因,在不同光周期下,不同亚家族基因的表达模式存在差异,表明PmPRRs对糜子响应光周期变化起重要的调控作用。

关键词: 糜子, 伪响应调节蛋白, 光周期, 生物信息学, 实时荧光定量PCR

Abstract:

Objective Pseudo-response regulators (PRRs) play crucial roles in regulating circadian rhythms and flowering time in plants. This study aimed to systematically identify the PRR gene family in broomcorn millet (Panicum miliaceum L.) at the whole-genome level, providing a theoretical basis for understanding their biological functions. Method Bioinformatics methods were employed to analyze the physicochemical properties, conserved motifs, gene structures, collinearity, and phylogenetic relationships of the PRR gene family in broomcorn millet. The expression patterns of PRR genes under different photoperiod treatments were investigated using real-time quantitative PCR (RT-qPCR). Result A total of seven PRR genes were identified from the broomcorn millet genome, designated as PmPRR1 to PmPRR7, which were unevenly distributed across five chromosomes. Phylogenetic analysis revealed that the PmPRR genes belong to Group 1 to Group 3 subfamilies. Analysis of conserved protein motifs showed that six genes contained Motif1, Motif2, and Motif3, indicating high conservation among them. Promoter cis-acting element analysis suggested that PmPRR genes are associated with light response, plant growth and development, stress responses, and hormone regulation. RT-qPCR results demonstrated significant differences in the expressions of PmPRR genes under different photoperiod treatments (short-day, 8 h; intermediate-day, 14 h; long-day, 16 h). Conclusion This study identified seven PmPRR genes. The expression patterns of genes from different subfamilies vary under different photoperiods, indicating that PmPRRs play an important regulatory role in the response of broomcorn millet to photoperiod changes.

Key words: broomcorn millet, pseudo-response regulators, photoperiod, bioinformatics, RT-qPCR