耐盐砧木'抗砧3号'对葡萄微嫁接苗光合作用的影响OA
Effects of salt-tolerant rootstock'Kangzhen No.3'on photosynthesis of micro-grafted seedlings of grapevine
[目的]系统分析盐胁迫下葡萄耐盐砧木微嫁接苗光合作用的生理及分子响应机制,揭示耐盐砧木微嫁接调控葡萄耐盐性的潜在机制.[方法]以'黑比诺'盐敏感葡萄为接穗,耐盐的'抗砧3号'为砧木,通过微嫁接操作获得嫁接苗,将'黑比诺'自根苗、'抗砧 3号'自根苗及嫁接苗 3种葡萄苗移栽到花盆中生长 30 d后,用 200 mmol/L NaCl处理6 d,测定并比较盐胁迫下'黑比诺'自根苗和嫁接苗叶片的光合气体交换参数(Pn、Gs、Tr、Ci)、相对叶绿素含量(SPAD)和叶绿素荧光参数(F0、Fm、Fv/Fm)的变化,并通过转录组测序分析'黑比诺'自根苗和嫁接苗差异表达基因(DEGs)及其响应特征,基于GO数据库和KEGG数据库对DEGs进行基因功能注释,选择6个DEGs进行RT-qPCR分析,以验证其与转录组数据的匹配性.[结果]在200 mmol/L NaCl处理6 d后,与'黑比诺'自根苗相比,嫁接苗Pn、Gs、Tr、Ci、SPAD、F0、Fm、Fv/Fm分别显著提升了101.2%,51.9%,51.4%,81.1%,40.7%,58.4%,51.5%和26.9%.盐胁迫下嫁接苗和'黑比诺'接穗自根苗共有2 704个共同DEGs.这些DEGs主要富集于生物过程、分子功能和细胞组分3大类别,显著富集于光合作用-天线蛋白通路、光合作用通路和光合生物中的碳固定等通路,光合通路中关键基因 LHCA6、LHCA5、LHCB4.1、LHCB5、ATPG、ATPD、ATPC、GAPC2和 GAPC在嫁接苗中显著上调表达.RT-qPCR表明,盐胁迫下嫁接苗中关键差异基因LHCA5、LHCB5、A T P D、A T P C、G A P C2、GAPCP1的相对表达水平与转录组测序TPM值变化趋势一致,佐证了转录组数据的可靠性.[结论]在盐胁迫条件下,葡萄嫁接苗光合通路中关键基因上调表达,光能捕获、电子传递效率和ATP/NADPH合成增强,Calvin循环中的碳固定过程得到优化,光能利用效率与碳固定能力增强,光合性能得到显著改善.
[Objective]This research aims to systematically analyze the physiological and molecular re-sponse mechanisms of photosynthesis in salt-tolerant grape rootstock micro-grafted seedlings under salt stress,to reveal the potential mechanisms by which salt-tolerant rootstock micrografting regulates grape salt tolerance.[Method]With'Pinot Noir',a salt-sensitive grape variety,as the scion and'Kangzhen No.3',which was salt-tolerant,as the rootstock,grafted seedlings were obtained through micrografting operations.Three types of grape seedlings,including'Pinot Noir'own-rooted seedlings,'Kangzhen No.3'own-rooted seedlings,and grafted seedlings,were transplanted into flowerpots and cultivated for 30 days,then they were treated with 200 mmol/L NaCl for 6 days.The changes in photosynthetic gas exchange parameters(Pn,Gs,Tr,Ci),relative chlo-rophyll content(SPAD),and chlorophyll fluorescence parameters(F0,Fm,Fv/Fm)in the leaves of own-rooted'Pinot Noir'seedlings and grafted seedlings under salt stress were determined and compared.Transcriptome se-quencing was performed to analyze the differentially expressed genes(DEGs)and their response characteristics between own-rooted'Pinot Noir'seedlings and grafted seedlings.Gene functional annotations of DEGs were conducted based on the GO database and KEGG database.Six DEGs were selected for RT-qPCR analysis to verify their consistency with the transcriptome data.[Result]After 6 days of treatment with 200 mmol/L NaCl,Pn,Gs,Tr,Ci,SPAD,F0,Fm and Fv/Fm of the grafted seedlings were significantly increased by 101.2%,51.9%,51.4%,81.1%,40.7%,58.4%,51.5%and 26.9%respectively,compared with those of the own-rooted seed-lings of'Pinot Noir'.Transcriptome sequencing analysis revealed 2 704 common DEGs between grafted seed-lings and'Pinot Noir'own-rooted seedlings under salt stress.GO functional annotation showed that these DEGs were mainly enriched in three categories:biological processes,molecular functions,and cellular compo-nents.KEGG analysis indicated that they were significantly enriched in pathways such as photosynthesis-an-tenna proteins pathway,photosynthesis pathway,and pathway of carbon fixation in photosynthetic organisms.Key genes in photosynthetic pathways,including LHCA6,LHCA5,LHCB4.1,LHCB5,ATPG,ATPD,ATPC,GAPC2,and GAPC,were significantly upregulated in grafted seedlings.The RT-qPCR results showed that the relative expression levels of key DEGs LHCA5,LHCB5,ATPD,ATPC,GAPC2,and GAPCP1 in grafted seedlings under salt stress were consistent with the change trends of TPM values in transcriptome se-quencing,confirming the reliability of the transcriptome data.[Conclusion]Under salt stress conditions,key genes in the photosynthetic pathway of grafted seedlings were up-regulated,enhancing light energy capture,electron transport efficiency,and ATP/NADPH synthesis,optimizing the carbon fixation process in the Calvin cycle,improving light energy utilization and carbon fixation capacity,which indicated that the photosynthetic per-formance was significantly enhanced.
来英;乃国洁;闫浩凯;马蕾;李胜;马绍英
甘肃农业大学 生命科学技术学院,甘肃 兰州 730070甘肃农业大学 园艺学院,甘肃 兰州 730070甘肃农业大学 园艺学院,甘肃 兰州 730070甘肃农业大学 园艺学院,甘肃 兰州 730070甘肃农业大学 生命科学技术学院,甘肃 兰州 730070||甘肃农业大学 园艺学院,甘肃 兰州 730070||甘肃省干旱生境作物学重点实验室,甘肃 兰州 730070甘肃农业大学 实验室与实践基地管理中心,甘肃 兰州 730070
农业科技
葡萄耐盐砧木微嫁接盐胁迫光合作用叶绿素荧光转录组分析
grapevinesalt-tolerant rootstockmicro-graftingsalt stressphotosynthesischlorophyll fluo-rescencetranscriptome analysis
《西北农林科技大学学报(自然科学版)》 2026 (6)
170-180,11
中央引导地方科技发展资金项目(25ZYJA033)甘肃省重点人才项目(2023RCXM23)
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