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菠萝AcCAX1克隆及表达分析

陈金绘 李川玲 张秀梅 姚艳丽 王文波 谭丹 吴青松 贺军军 朱祝英 付琼 徐娟

山西农业大学学报(自然科学版)2025,Vol.45Issue(1):52-60,9.
山西农业大学学报(自然科学版)2025,Vol.45Issue(1):52-60,9.DOI:10.13842/j.cnki.issn1671-8151.202406027

菠萝AcCAX1克隆及表达分析

Identification and expression analysis of pineapple AcCAX1

陈金绘 1李川玲 2张秀梅 2姚艳丽 2王文波 2谭丹 2吴青松 2贺军军 2朱祝英 2付琼 2徐娟3

作者信息

  • 1. 华中农业大学 园艺林学学院,湖北 武汉 430070||中国热带农业科学院 南亚热带作物研究所/农业农村部热带果树生物学重点实验室/海南省热带园艺产品采后生理与保鲜重点实验室,广东 湛江 524091
  • 2. 中国热带农业科学院 南亚热带作物研究所/农业农村部热带果树生物学重点实验室/海南省热带园艺产品采后生理与保鲜重点实验室,广东 湛江 524091
  • 3. 华中农业大学 园艺林学学院,湖北 武汉 430070
  • 折叠

摘要

Abstract

[Objective]This study aimed to clone and identify the Ca2+/H+antiport protein AcCAX1 in pineapple,analyze its full-length sequence and expression profile,and establish a foundation for functional studies of this gene.[Methods]The Ac-CAX1 sequence was obtained through PCR amplification techniques,and its protein structure,sequence alignment,and phylo-genetic relationships were analyzed using bioinformatics tools.Real-time fluorescence quantitative PCR(qPCR)was employed to assess the response of AcCAX1 to different ion,temperature stress,and plant hormones.[Results]AcCAX1 has an open reading frame of 1428 base pairs and encodes a stable hydrophobic protein consisting of 514 amino acids with a relative molecu-lar mass of 50 801.11 Da and a theoretical isoelectric point of 6.24.Sequence analysis revealed that the amino acid sequence of AcCAX1 contained 11 typical trans-membrane domains,including two Ca2+/H+antiporter domains.Secondary structure predi-cations revealed that the α-helix constituted the largest proportion of the CAX1 protein structure at 58.74%,followed by irregu-lar coils(21.68%),elongation chains(14.95%),and β-sheets(4.63%).Real-time qPCR analysis showed that the tran-script level of AcCAX1 was upregulated by exogenous CaCl2 and NaCl treatments,while MnCl2 treatment led to a decrease in transcript levels.Spatial expression analysis revealed that AcCAX1 exhibited higher expression levels in older leaves and stems but lower levels in fruits and flower buds.Subcellular localization in tobacco showed that AcCAX1 was expressed in the cell membrane,cytoplasm,and nucleus.In addition,the promoter region of AcCAX1 contained a large number of abiotic stress re-sponse elements.The transcript level of AcCAX1 was significantly down-regulated under both cold and heat stress conditions.[Conclusion]The Ca2+/H+antiport protein AcCAX1 in pineapple likely plays a significant role in the plant's response to abiot-ic stresses.

关键词

菠萝/AcCAX1/Ca2+/H+反向转运蛋白/基因表达/胁迫响应

Key words

Pineapple/AcCAX1/Ca2+/H+antiporter/Gene expression/Stress response

分类

农业科技

引用本文复制引用

陈金绘,李川玲,张秀梅,姚艳丽,王文波,谭丹,吴青松,贺军军,朱祝英,付琼,徐娟..菠萝AcCAX1克隆及表达分析[J].山西农业大学学报(自然科学版),2025,45(1):52-60,9.

基金项目

中央级公益性科研院所基本科研业务费专项(1630062024007) (1630062024007)

海南省自然科学基金(324MS101) (324MS101)

山西农业大学学报(自然科学版)

OA北大核心

1671-8151

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