首页|筇竹K+通道蛋白QtKCO1基因的克隆与表达分析

筇竹K+通道蛋白QtKCO1基因的克隆与表达分析

扫码查看
为分析KCO家族基因在筇竹钾运输中起到的重要作用,本研究以筇竹实生苗(2年生)为试材,利用RACE技术,克隆出KCO家族基因,命名为QtKCO1(基因登录号:MT078981),并分析其表达特征.结果表明,QtKCO1基因全长为1 502 bp,开放阅读框为1 041 bp,编码347个氨基酸.QtKCO1具有5个跨膜区域,且与野生二粒小麦(Triticum dicoccoides)的同源性最高,为85.88%.另外,QtKCO1基因是组成型表达,在筇竹每个组织器官(竹笋,根,茎,叶)均有表达,表达量依次为竹笋>茎>叶>根.高浓度KC1胁迫下,随着处理时间的增加,QtKCO1基因在根表达量增加,而在茎和叶中表达量则下降.与对照组相比,NaCl胁迫处理条件下,筇竹QtKCO1在筇竹各个组织器官中均呈现上调表达,且表达量依次为叶>茎>根.本研究为进一步分析KCO家族基因在钾运输中的作用提供了理论依据.
Cloning and Expression Analysis on QtKCO1 Gene from Qiongzhuea tu-midinoda
In order to study the important role of KCO family genes in potassium transport of Qiongzhuea tu-midinoda,the KCO gene was cloned from the 2-year-old seedlings of Qiongzhuea tumidinoda by RACE technique.The gene was named QtKCO1(GenBank number:MT078981)and its expression characteristics were analyzed.The results showed that the full length of QtKCO1 gene was 1 502 bp,and the open reading frame(ORF)of QtKCO1 was 1 041 bp,encoding 347 amino acids.QtKCO1 had five transmembrane regions and showed the highest homol-ogy of 85.88%with wild two-grain wheat(Triticum dicoccoides).expressed compositionally in all tissues and organs(bamboo shoots,roots,stems,leaves),and the expression levels were in the order of bamboo shoots>stems>leaves>roots.Under high concentration KC1 stress,the expression of QtKCO1 gene increased in roots,but de-creased in stems and leaves with the increase of treatment time.Compared with the control group,QtKCO1 expres-sion was up-regulated in all tissues and organs of Qiongzhuea tumidinoda under NaCl stress,and the expression level was in the order of leaves>stems>roots.This study provides a theoretical basis for further analysis of the role of KCO family genes in potassium transport.

Outward rectifying K+channelQiongzhuea tumidinodaQtKCO1StressGene cloning and expression

张倩、张馨艺、芮蕊、王澍

展开 >

西南林业大学园林园艺学院,国家林业局西南风景园林工程技术研究中心,昆明,650224

西南林业大学土木工程学院,昆明,650224

外向整流型钾离子通道 筇竹 QtKCO1 胁迫 基因克隆和表达

云南省农业基础研究联合专项农业联合青年项目

018FG001-073

2024

分子植物育种
海南省生物工程协会

分子植物育种

CSTPCD北大核心
影响因子:0.765
ISSN:1672-416X
年,卷(期):2024.22(17)