生物技术通报 ›› 2026, Vol. 42 ›› Issue (11): 154-163.doi: 10.13560/j.cnki.biotech.bull.1985.2026-0186

• 研究报告 • 上一篇    

紫花苜蓿MsCZF29基因克隆及耐冻功能分析

范雨馨1, 任乃芃2, 轩一芙1, 臧辉1, 刘香萍1()   

  1. 1.黑龙江八一农垦大学动物科技学院,大庆 163319
    2.黑龙江八一农垦大学农学院,大庆 163319
  • 收稿日期:2026-02-06 出版日期:2026-11-26 发布日期:2026-11-03
  • 通讯作者: 刘香萍lxp3885@126.com
  • 基金资助:
    农业生物育种国家科技重大专项(2022ZD04012)

Cloning and Freezing Tolerance Analysis of the MsCZF29 Gene in Alfalfa

FAN Yu-xin1, REN Nai-peng2, XUAN Yi-fu1, ZANG Hui1, LIU Xiang-ping1()   

  1. 1.College of Animal Science and Technology, Heilongjiang Bayi Agricultural University, Daqing 163319
    2.College of Agriculture, Heilongjiang Bayi Agricultural University, Daqing 163319
  • Received:2026-02-06 Published:2026-11-26 Online:2026-11-03

摘要:

目的 CZF锌指蛋白(Zinc finger proteins, ZFPs)在植物响应生物及非生物胁迫中起到重要的调控作用。克隆紫花苜蓿MsCZF29基因并分析其耐冻功能,为揭示该基因调控拟南芥耐冻机制奠定基础。 方法 以拟南芥为材料,根据前期紫花苜蓿抗冻转录组分析,筛选得到1个冷冻胁迫响应基因,将其克隆出来并命名为MsCZF29,并进行生物信息学分析和表型分析;构建过表达载体通过农杆菌转化法获得转基因植株(OE2-1、OE2-2和OE6-2)。观察冷冻胁迫下T3代存活率表型、测定生理生化指标和相关冷响应基因的表达量;进行转录自激活活性验证。 结果 MsCZF29编码区序列(CDS)全长为1 554 bp,编码517个氨基酸,是不稳定亲水蛋白。亚细胞定位发现该蛋白定位于细胞核,酵母自激活实验发现其具有转录激活活性。异源过表达MsCZF29显著增加了冷冻胁迫下拟南芥株系的过氧化氢酶(catalase, CAT)、超氧化物歧化酶(superoxide dismutase, SOD)和过氧化物酶(peroxidase, POD)活性,降低了相对电导率(REL)和丙二醛(MDA)含量。冷冻胁迫下过表达株系的存活率及生长状态明显优于野生型。 结论 成功克隆MsCZF29基因,其过表达在冷冻胁迫过程中发挥正向调控作用,可提高植物的耐冻性。

关键词: 紫花苜蓿, MsCZF29, 冷冻胁迫, 耐冻性, 生理指标

Abstract:

Objective CZF zinc finger proteins (ZFPs) play important regulatory roles in plant responses to biotic and abiotic stresses. Cloning the MsCZF29 gene from alfalfa and analyzing its freezing tolerance function lays a foundation for revealing the regulatory mechanism of this gene in freezing tolerance of Arabidopsis. Method Using Arabidopsis thaliana as the experimental model, we identified the freezing stress-responsive gene MsCZF29 based on previous transcriptomic analysis of cold tolerance in Medicago sativa. The gene was cloned and designated as MsCZF29, and bioinformatics analysis and phenotypic characterization were conducted on it. An overexpression vector was constructed and introduced into plants via Agrobacterium-mediated transformation to generate transgenic lines (OE2-1, OE2-2, and OE6-2). Under freezing stress conditions, we evaluated T3 generation survival rates, measured key physiological and biochemical parameters, and quantified expression levels of relevant cold-responsive genes. Transcriptional autoactivation activity was verified using yeast assays. Result The MsCZF29 coding sequence (CDS) spans 1 554 bp, encoding 517 amino acids that form a protein which is both unstable and hydrophilic. Subcellular localization confirmed that the protein is localized in the nucleus, while yeast autoactivation assays demonstrated its transcriptional activation capability. Heterologous overexpression of MsCZF29 significantly enhanced the activities of catalase (CAT), superoxide dismutase (SOD), and peroxidase (POD) in Arabidopsis lines under freezing stress, while simultaneously reducing relative electrical conductivity (REL) and malondialdehyde (MDA) content. Transgenic lines exhibited markedly higher survival rates and superior growth status compared to wild-type plants under freezing stress conditions. Conclusion We successfully cloned MsCZF29 gene, demonstrating that its overexpression exerts a positive regulatory effect during freezing stress responses, thereby enhancing plant freezing tolerance.

Key words: alfalfa, MsCZF29 gene, freezing stress, freezing resistance, physiological indicators