Protein Phosphatase 2A B'α and B'β promote pollen wall construction partially through BZR1-activated CEP1 in Arabidopsis.

IF 5.6 2区 生物学 Q1 PLANT SCIENCES Journal of Experimental Botany Pub Date : 2025-01-11 DOI:10.1093/jxb/eraf004
Ying-Jie Gao, Yu-Lan Zhang, Wen-Hui Wang, Ammara Latif, Yue-Tian Wang, Wen-Qiang Tang, Cui-Xia Pu, Ying Sun
{"title":"Protein Phosphatase 2A B'α and B'β promote pollen wall construction partially through BZR1-activated CEP1 in Arabidopsis.","authors":"Ying-Jie Gao, Yu-Lan Zhang, Wen-Hui Wang, Ammara Latif, Yue-Tian Wang, Wen-Qiang Tang, Cui-Xia Pu, Ying Sun","doi":"10.1093/jxb/eraf004","DOIUrl":null,"url":null,"abstract":"<p><p>A well-constructed pollen wall is essential for pollen fertility, which relies on the contribution of tapetum. Our results demonstrate an essential role of the tapetum-expressed protein phosphatase 2A (PP2A) B'α and B'β in pollen wall formation. The b'aβ double mutant pollen grains harbored sticky remnants and tectum breakages, resulting in failed release. B'α and B'β function partially through dephosphorylating and activating BZR1. The bzr1 bes1 double and higher-order mutants of this family displayed similar defects in pollen wall, while bzr1-1D, having an active mBZR1 exhibited fertile pollen grains in a B'α and B'β dependent manner. Correspondingly, the level of phospho-BZR1 is increased and dephospho-BZR1 is decreased in b'aβ and bzr1-1D/b'aβ at anther stages 8-9 as compared with Col-0 and bzr1-1D, respectively. A cysteine protease gene CEP1 was identified as a BZR1 target, whose transcriptional activation necessitates BRREs in the promoter region and BZR1 DNA binding domain. The mRNA level of CEP1 at stages 8-9 was extremely low in bzr1 and bzr1 bes1, while higher in Col-0 and bzr1-1D depending on B'α and B'β. Furthermore, cep1 mutants displayed similar defects in pollen wall. In brief, this study uncovered a PP2A-BZR1-CEP1 regulatory module, providing a new insight into pollen maturation mechanism.</p>","PeriodicalId":15820,"journal":{"name":"Journal of Experimental Botany","volume":" ","pages":""},"PeriodicalIF":5.6000,"publicationDate":"2025-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Experimental Botany","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/jxb/eraf004","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

A well-constructed pollen wall is essential for pollen fertility, which relies on the contribution of tapetum. Our results demonstrate an essential role of the tapetum-expressed protein phosphatase 2A (PP2A) B'α and B'β in pollen wall formation. The b'aβ double mutant pollen grains harbored sticky remnants and tectum breakages, resulting in failed release. B'α and B'β function partially through dephosphorylating and activating BZR1. The bzr1 bes1 double and higher-order mutants of this family displayed similar defects in pollen wall, while bzr1-1D, having an active mBZR1 exhibited fertile pollen grains in a B'α and B'β dependent manner. Correspondingly, the level of phospho-BZR1 is increased and dephospho-BZR1 is decreased in b'aβ and bzr1-1D/b'aβ at anther stages 8-9 as compared with Col-0 and bzr1-1D, respectively. A cysteine protease gene CEP1 was identified as a BZR1 target, whose transcriptional activation necessitates BRREs in the promoter region and BZR1 DNA binding domain. The mRNA level of CEP1 at stages 8-9 was extremely low in bzr1 and bzr1 bes1, while higher in Col-0 and bzr1-1D depending on B'α and B'β. Furthermore, cep1 mutants displayed similar defects in pollen wall. In brief, this study uncovered a PP2A-BZR1-CEP1 regulatory module, providing a new insight into pollen maturation mechanism.

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
蛋白磷酸酶2A B′α和B′β通过bzr1激活的CEP1部分促进拟南芥花粉壁构建。
良好的花粉壁是花粉繁殖力的基础,而花粉繁殖力依赖于绒毡层的贡献。我们的研究结果表明,绒毡层表达的蛋白磷酸酶2A (PP2A) B'α和B'β在花粉壁形成中起重要作用。b’aβ双突变体花粉粒存在粘性残余物和顶盖破损,导致释放失败。B'α和B'β通过去磷酸化和激活BZR1发挥部分功能。该家族的双级突变体bzr1 bes1和高阶突变体在花粉壁上表现出类似的缺陷,而具有活性mBZR1的bzr1- 1d在B'α和B'β依赖的情况下表现出可育的花粉粒。与Col-0和bzr1-1D相比,8-9花药期b'aβ和bzr1-1D/b'aβ中磷酸化- bzr1水平升高,去磷酸化- bzr1水平降低。一个半胱氨酸蛋白酶基因CEP1被确定为BZR1的靶标,其转录激活需要启动子区域和BZR1 DNA结合域的BRREs。8-9期,CEP1 mRNA水平在bzr1和bzr1 bes1中极低,而在Col-0和bzr1- 1d中较高,这取决于B'α和B'β。此外,cep1突变体在花粉壁上也表现出类似的缺陷。总之,本研究揭示了PP2A-BZR1-CEP1调控模块,为花粉成熟机制的研究提供了新的视角。
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
Journal of Experimental Botany
Journal of Experimental Botany 生物-植物科学
CiteScore
12.30
自引率
4.30%
发文量
450
审稿时长
1.9 months
期刊介绍: The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology. Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.
期刊最新文献
Conserved and novel roles of the bHLH transcription factor SPATULA in tomato. Long-day induced flowering requires DNA hypermethylation in orchardgrass. DNA methylation dynamics in the shoot apical meristem. Nitric oxide as integral element in priming- induced tolerance and plant stress memory. Tissue-specific responses of the central carbon metabolism in tomato fruit to low oxygen stress.
×
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