杧果铁还原酶(FRO)编码基因的鉴定与表达模式分析OA北大核心CSTPCD
Identification and Expression Pattern Analysis of Ferric Reduction Oxidase Encoding Genes in Mango
铁(Fe)是植物生长发育的必需微量元素之一,参与植物体内多种生命活动和代谢过程.有关铁素吸收、转运和分配吸收的分子机制研究主要体现在一年生模式作物,果树中铁吸收与转运相关基因的生物学功能依然未知.本研究从二倍体杧果桂热 82 中克隆并鉴定了 11 个铁还原酶(FRO)编码基因,命名为MiFRO1~MiFRO11;除 MiFRO1缺失Motif2~Motif5 基序外,其他MiFROs均含有 10 个典型的Motif基序,除MiFRO3 具有独特的三级结构外,其他MiFROs拥有相近的三级结构;11 种不同科、属植物FRO蛋白的氨基酸水平一致性约为 42.07%,MiFROs的氨基酸水平一致性约为 62.43%;系统进化树表明 MiFROs 倾向于单独聚集在一起,在系统发育树上与其他 10 种植物的同源蛋白进化距离较远;实时荧光定量 PCR 表明MiFRO8在杧果树体中的整体表达水平最高,MiFRO4、MiFRO5、MiFRO8和MiFRO11在成年树体新生叶片和嫁接苗叶片中的表达量最高,MiFRO6和MiFRO7在成年树体新生韧皮部和嫁接苗茎部的表达水平最高,MiFRO1和MiFRO10在幼果的表达水平最高,MiFRO2和MiFRO9在嫁接苗根部的表达量最高,而MiFRO3在盛开期花朵中的表达量最高.此外,MiFROs在根部易受缺铁和NaCl胁迫的诱导而显著增加;MiFRO3、MiFRO5和MiFRO8受高铁毒害的抑制,表达量降低;MiFRO2、MiFRO5、MiFRO7受ABA胁迫,其表达量增加;MiFRO1、MiFRO5受PEG胁迫,其表达量增加,MiFRO2、MiFRO6和MiFRO7受低温(4℃)抑制,其表达量降低,但MiFROs对热胁迫(45℃)不敏感.本研究为明确杧果铁的吸收与转运机制提供基因资源,并为解析热带作物果树铁素营养与高效利用奠定理论基础.
Iron(Fe)is one of the essential trace mineral elements in plants to maintain normal growth and development that plays an important role in various life processes.Researches towards molecular mechanism of Fe uptake,transport and distribution are mainly focused on the annual model plants.Biological functions of genes towards Fe uptake and transport in fruit trees are still unknown.In this study,11 ferric reduction oxidase encoding genes(FROs)were isolated and identified from diploid mango Guire 82,named by MiFRO1-MiFRO11.All mango FRO had ten typical motifs ex-cept for MiFRO1 lacking Motif2-Motif5.All mango FRO possessed similar tertiary structure,with the exception that MiFRO3 exhibited distinct tertiary structure.The amino acid sequences of FRO from 11 plants shared an overall identity of 42.07% ,while mango FRO shared an overall identity of 62.43% .Phylogenetic tree analysis showed that mango FRO were prone to be closely clustered together lonely,which was far away from the homologs of the other ten plants in genetic distance.Quantitative real-time PCR(qRT-PCR)analysis showed that MiFRO3 was the most abundant ex-pressed gene during different parts of Guire 82 mango on the whole.In particular,MiFRO4,MiFRO5,MiFRO8 and MiFRO11 were highly expressed in the leaves of both mature trees and grafted seedlings.MiFRO6 and MiFRO7 were highly expressed in phloem or stem,MiFRO1 and MiFRO10 were highly expressed in young fruits,MiFRO2 and Mi-FRO9 were highly expressed in seedling roots,while MiFRO3 was highly expressed in full bloom flowers.In addition,expression of FRO in mango roots were mainly induced under iron depletion and NaCl stress,respectively,while Mi-FRO3,MiFRO5 and MiFRO8 were significantly reduced under iron toxicity.Expression of MiFRO2,MiFRO5 and Mi-FRO7 were increased under ABA treatment,and MiFRO1 and MiFRO5 were enhanced under PEG treatment.Expression of MiFRO2,MiFRO6 and MiFRO7 were decreased under low temperature(4℃ ).However,FRO changed little under heat stress(45℃ )in mango roots.This study would provide gene resources to elucidate the molecular mechanisms of Fe uptake and transport in mango,and lay a theoretical foundation to reveal Fe nutrition and high utilization in tropical fruit crops.
韩广栋;孙丰沛;任姿颖;曹晶雯;高爱平;黄建峰;宋志忠
鲁东大学农林工程研究院/山东省高校作物高产抗逆分子模块育种重点实验室,山东烟台 264025中国热带农业科学院热带作物品种资源研究所,海南海口 571101鲁东大学农林工程研究院/山东省高校作物高产抗逆分子模块育种重点实验室,山东烟台 264025||剑桥大学植物系,英国剑桥 CB2 3EA
园艺学与植物营养学
杧果铁吸收铁还原酶非生物胁迫表达模式
mangoFe uptakeferric reduction oxidaseabiotic stressexpression pattern
《热带作物学报》 2024 (002)
225-233 / 9
国家重点研究计划子课题(No.2019YFD1000504);国家自然科学基金项目(No.31501743);国家留学基金项目(No.202208370080).
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