引用本文:
【打印本页】   【下载PDF全文】   查看/发表评论  下载PDF阅读器  关闭
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览 2184次   下载 394 本文二维码信息
码上扫一扫!
北苍术HDR基因克隆及表达分析
王晓宇, 李肖慧, 闫会景, 玉猛, 王凤茹, 客绍英
河北农业大学 生命科学学院,河北 保定 071033
摘要:
【目的】克隆北苍术1-羟基-2-甲基-2-(-E-)-丁烯基-4-二磷酸还原酶基因(AcHDR),探究其生物学特征和不同组织及盐胁迫下的表达模式,为研究AcHDR功能提供理论依据。【方法】用RACE技术克隆AcHDR基因,分析AcHDR编码蛋白的理化性质、保守结构域、保守性及结构,构建系统发育树;用实时荧光定量PCR (RT-qPCR)技术检测AcHDR在不同组织及100 mmol/L NaCl胁迫处理不同时间下的表达量;测定不同盐胁迫下叶片的光合特性。【结果】AcHDR(GenBank登录号:PQ369427)开放阅读框全长为1 383 bp,编码460个氨基酸,具有lytB_ispH结构域,在进化过程中相对保守,与生菜、菊苣和橡胶草的HDR亲缘关系较近。RT-qPCR结果表明,AcHDR在北苍术叶中表达量最高;在100 mmol/L NaCl胁迫处理不同时间后,AcHDR表达量呈现先升高后降低的趋势。150 和250 mmol/L NaCl胁迫显著降低了北苍术光合特性。【结论】AcHDR基因快速响应盐胁迫,可能会提高植物的耐盐性。
关键词:  北苍术  HDR  qRT-PCR  RACE技术
DOI:10.13207/j.cnki.jnwafu.2025.12.021
分类号:
基金项目:河北省中央引导地方科技发展资金项目“自由探索类基础研究”(246Z2512G)
Cloning and expression analysis of the HDR gene in Atractylodes chinensis (DC.) Koidz.
WANG Xiaoyu, LI Xiaohui, YAN Huijing, YU Meng, WANG Fengru, KE Shaoying
College of Life Sciences,Agricultural University of Hebei,Baoding,Hebei 071033,China
Abstract:
【Objective】The study aimed to clone the HDR gene from Atractylodes chinensis (DC.) Koidz. and investigate its biological characteristics and expression patterns in different tissues and under salt stress,providing a theoretical basis for studying the functional role of the AcHDR gene.【Method】The AcHDR gene was cloned using RACE technology.The physicochemical properties,conserved domains,conservation,and structure of the AcHDR-encoded protein were analyzed,and a phylogenetic tree was constructed.The expression of AcHDR in different tissues and under 100 mmol/L NaCl stress at different time points was detected using RT-qPCR technology.The photosynthetic characteristics of leaves under different salt stress levels were also determined.【Result】The full-length open reading frame of AcHDR is 1 383 bp (GenBank accession number:PQ369427),encoding 460 amino acids,and contains a lytB_ispH domain.It is relatively conserved during evolution and closely related to HDR genes from lettuce,chicory,and rubber grass.RT-qPCR results indicated that AcHDR is most highly expressed in the leaves of A.chinensis.Under 100 mmol/L NaCl stress at different time points,the expression of AcHDR initially increased and then decreased.Salt stress at 150 and 250 mmol/L NaCl significantly reduced the photosynthetic characteristics of A.chinensis.【Conclusion】The rapid response of the AcHDR gene to salt stress may enhance the salt tolerance of plants.
Key words:  Atractylodes chinensis (DC.) Koidz.  HDR  RT qPCR  RACE technology