Analysis of expression characteristics and identification of interaction proteins of transcription factor BnaABI5 in Brassica napus.

Q3 Medicine 遗传 Pub Date : 2024-09-01 DOI:10.16288/j.yczz.24-064
Qian-Qian Ao, Fang-Xiao Lu, Liu-Qing Yang, Chun Li, Zeng-Kang Zhai, Dong-Ye Jia, Yuan-Qing Jiang, Bo Yang
{"title":"Analysis of expression characteristics and identification of interaction proteins of transcription factor BnaABI5 in <i>Brassica napus</i>.","authors":"Qian-Qian Ao, Fang-Xiao Lu, Liu-Qing Yang, Chun Li, Zeng-Kang Zhai, Dong-Ye Jia, Yuan-Qing Jiang, Bo Yang","doi":"10.16288/j.yczz.24-064","DOIUrl":null,"url":null,"abstract":"<p><p>Rapeseed is one important oil crop in China. However, its planting benefit is frequently affected by environmental stresses such as drought in the northwest region of China. The abscisic acid(ABA) signaling pathway plays an important role in plant abiotic stress response and tolerance, and ABFs/AREBs(ABA-responsive element binding factors/ABA-responsive element binding proteins) are the core transcription factors that regulate the expression of ABA-responsive genes. To dissect the key transcription factors mediated abiotic stress, we mainly characterized abscisic acid insensitive 5(BnaABI5) in rapeseed, including its subcellular localization, expression pattern in response to various stress and tissue-specific expression analysis, transcriptional activity analysis as well as interaction screening with BnaMPKs(mitogen-activated protein kinases). Our results showed that the BnaABI5-GFP fusion protein was localized in the nucleus, and its transcript level is induced by drought stress and was mainly expressed in the roots of rapeseed. Furthermore, BnaABI5 showed transcriptional activation activity through a yeast transactivation assay and it also activated the promoter activity of <i>EM6</i> target gene in the transient expression system in tobacco leaves. Moreover, BnaABI5 interacted with BnaMPK6 and BnaMPK13 through BiFC and Y2H analysis. This study preliminarily explored the expression characteristics of transcription factor BnaABI5 and its interaction with BnaMPKs, which might help us for further understanding the function of BnaABI5.</p>","PeriodicalId":35536,"journal":{"name":"遗传","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"遗传","FirstCategoryId":"1091","ListUrlMain":"https://doi.org/10.16288/j.yczz.24-064","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Rapeseed is one important oil crop in China. However, its planting benefit is frequently affected by environmental stresses such as drought in the northwest region of China. The abscisic acid(ABA) signaling pathway plays an important role in plant abiotic stress response and tolerance, and ABFs/AREBs(ABA-responsive element binding factors/ABA-responsive element binding proteins) are the core transcription factors that regulate the expression of ABA-responsive genes. To dissect the key transcription factors mediated abiotic stress, we mainly characterized abscisic acid insensitive 5(BnaABI5) in rapeseed, including its subcellular localization, expression pattern in response to various stress and tissue-specific expression analysis, transcriptional activity analysis as well as interaction screening with BnaMPKs(mitogen-activated protein kinases). Our results showed that the BnaABI5-GFP fusion protein was localized in the nucleus, and its transcript level is induced by drought stress and was mainly expressed in the roots of rapeseed. Furthermore, BnaABI5 showed transcriptional activation activity through a yeast transactivation assay and it also activated the promoter activity of EM6 target gene in the transient expression system in tobacco leaves. Moreover, BnaABI5 interacted with BnaMPK6 and BnaMPK13 through BiFC and Y2H analysis. This study preliminarily explored the expression characteristics of transcription factor BnaABI5 and its interaction with BnaMPKs, which might help us for further understanding the function of BnaABI5.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
分析甘蓝型油菜转录因子 BnaABI5 的表达特征并鉴定其相互作用蛋白
油菜籽是中国重要的油料作物之一。然而,在中国西北地区,其种植效益经常受到干旱等环境胁迫的影响。脱落酸(ABA)信号通路在植物非生物胁迫响应和耐受中起着重要作用,而ABFs/AREBs(ABA反应元件结合因子/ABA反应元件结合蛋白)是调控ABA反应基因表达的核心转录因子。为了研究介导非生物胁迫的关键转录因子,我们主要对油菜中脱落酸不敏感5(BnaABI5)进行了表征,包括其亚细胞定位、对各种胁迫响应的表达模式和组织特异性表达分析、转录活性分析以及与BnaMPKs(丝裂原活化蛋白激酶)的相互作用筛选。结果表明,BnaABI5-GFP融合蛋白定位于细胞核,其转录水平受干旱胁迫诱导,主要在油菜根部表达。此外,通过酵母转录激活试验,BnaABI5显示出转录激活活性,在烟草叶片瞬时表达系统中,它也激活了EM6靶基因的启动子活性。此外,通过BiFC和Y2H分析,BnaABI5还与BnaMPK6和BnaMPK13相互作用。本研究初步探讨了转录因子BnaABI5的表达特征及其与BnaMPKs的相互作用,这可能有助于我们进一步了解BnaABI5的功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
遗传
遗传 Medicine-Medicine (all)
CiteScore
2.50
自引率
0.00%
发文量
6699
期刊介绍:
期刊最新文献
Advancements and prospects in reconstructing the genetic genealogies of ancient and modern human populations using ancestral recombination graphs. Advances in high throughput sequencing methods for DNA damage and repair. Application of Mendelian randomization analysis in investigating the genetic background of blood biomarkers for colorectal cancer. Computational dissection of the regulatory mechanisms of aberrant metabolism in remodeling the microenvironment of breast cancer. Gut metagenome-derived image augmentation and deep learning improve prediction accuracy of metabolic disease classification.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1