Integrative physiological and transcriptome analysis unravels the mechanism of low nitrogen use efficiency in burley tobacco.

IF 2.3 3区 生物学 Q2 PLANT SCIENCES Plant Direct Pub Date : 2024-10-20 eCollection Date: 2024-10-01 DOI:10.1002/pld3.70004
Yuqing Feng, Yuanyuan Zhao, Yanjun Ma, Xiaolong Chen, Hongzhi Shi
{"title":"Integrative physiological and transcriptome analysis unravels the mechanism of low nitrogen use efficiency in burley tobacco.","authors":"Yuqing Feng, Yuanyuan Zhao, Yanjun Ma, Xiaolong Chen, Hongzhi Shi","doi":"10.1002/pld3.70004","DOIUrl":null,"url":null,"abstract":"<p><p>Burley tobacco, a chlorophyll-deficient mutant with impaired nitrogen use efficiency (NUE), generally requires three to five times more nitrogen fertilization than flue-cured tobacco to achieve a comparable yield, which generates serious environmental pollution and negatively affects human health. Therefore, exploring the mechanisms underlying NUE is an effective measure to reduce environmental pollution and an essential direction for burley tobacco plant improvement. Physiological and genetic factors affecting tobacco NUE were identified using two tobacco genotypes with contrasting NUE in hydroponic experiments. Nitrogen use inefficient genotype (TN90) had lower nitrogen uptake and transport efficiencies, reduced leaf and root biomass, lower nitrogen assimilation and photosynthesis capacity, and lower nitrogen remobilization ability than the nitrogen use efficient genotype (K326). Transcriptomic analysis revealed that genes associated with photosynthesis, carbon fixation, and nitrogen metabolism are implicated in NUE. Three nitrate transporter genes in the leaves (<i>NPF2.11</i>, <i>NPF2.13</i>, and <i>NPF3.1</i>) and three nitrate transporter genes (<i>NPF6.3</i>, <i>NRT2.1</i>, and <i>NRT2.4</i>) in roots were down-regulated by nitrogen starvation, all of which showed lower expression in TN90 than in K326. In addition, the protein-protein interaction (PPI) network diagram identified eight key genes (<i>TPIP1</i>, <i>GAPB</i>, <i>HEMB</i>, <i>PGK3</i>, <i>PSBO</i>, <i>PSBP2</i>, <i>PSAG</i>, and <i>GLN2</i>) that may affect NUE. Less advantageous changes in nitrogen uptake, nitrogen assimilation in combination with nitrogen remobilization, and maintenance of photosynthesis in response to nitrogen deficiency led to a lower NUE in TN90. The key genes (<i>TPIP1</i>, <i>GAPB</i>, <i>PGK3</i>, <i>PSBO</i>, <i>PSBP2</i>, <i>PSAG</i>, and <i>GLN2</i>) were associated with improving photosynthesis and nitrogen metabolism in tobacco plants grown under N-deficient conditions.</p>","PeriodicalId":20230,"journal":{"name":"Plant Direct","volume":"8 10","pages":"e70004"},"PeriodicalIF":2.3000,"publicationDate":"2024-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11491304/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Direct","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1002/pld3.70004","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Burley tobacco, a chlorophyll-deficient mutant with impaired nitrogen use efficiency (NUE), generally requires three to five times more nitrogen fertilization than flue-cured tobacco to achieve a comparable yield, which generates serious environmental pollution and negatively affects human health. Therefore, exploring the mechanisms underlying NUE is an effective measure to reduce environmental pollution and an essential direction for burley tobacco plant improvement. Physiological and genetic factors affecting tobacco NUE were identified using two tobacco genotypes with contrasting NUE in hydroponic experiments. Nitrogen use inefficient genotype (TN90) had lower nitrogen uptake and transport efficiencies, reduced leaf and root biomass, lower nitrogen assimilation and photosynthesis capacity, and lower nitrogen remobilization ability than the nitrogen use efficient genotype (K326). Transcriptomic analysis revealed that genes associated with photosynthesis, carbon fixation, and nitrogen metabolism are implicated in NUE. Three nitrate transporter genes in the leaves (NPF2.11, NPF2.13, and NPF3.1) and three nitrate transporter genes (NPF6.3, NRT2.1, and NRT2.4) in roots were down-regulated by nitrogen starvation, all of which showed lower expression in TN90 than in K326. In addition, the protein-protein interaction (PPI) network diagram identified eight key genes (TPIP1, GAPB, HEMB, PGK3, PSBO, PSBP2, PSAG, and GLN2) that may affect NUE. Less advantageous changes in nitrogen uptake, nitrogen assimilation in combination with nitrogen remobilization, and maintenance of photosynthesis in response to nitrogen deficiency led to a lower NUE in TN90. The key genes (TPIP1, GAPB, PGK3, PSBO, PSBP2, PSAG, and GLN2) were associated with improving photosynthesis and nitrogen metabolism in tobacco plants grown under N-deficient conditions.

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
生理和转录组的综合分析揭示了布里烟草氮利用效率低的机理。
伯力烟草(Burley tobacco)是一种叶绿素缺乏的突变体,其氮素利用效率(NUE)较低,一般需要比烟叶烘烤烟草多三到五倍的氮肥才能获得相当的产量,从而产生严重的环境污染,并对人类健康产生不利影响。因此,探索氮利用效率的内在机理是减少环境污染的有效措施,也是改良毛蕊花烟草的重要方向。在水培实验中,利用两种氮利用效率截然不同的烟草基因型,确定了影响烟草氮利用效率的生理和遗传因素。与氮利用效率高的基因型(K326)相比,氮利用效率低的基因型(TN90)的氮吸收和运输效率较低,叶片和根的生物量减少,氮同化和光合作用能力较低,氮再移动能力较低。转录组分析表明,与光合作用、碳固定和氮代谢相关的基因与氮利用效率有关。叶片中的三个硝酸盐转运体基因(NPF2.11、NPF2.13 和 NPF3.1)和根系中的三个硝酸盐转运体基因(NPF6.3、NRT2.1 和 NRT2.4)受氮饥饿影响而下调,这些基因在 TN90 中的表达量均低于 K326。此外,蛋白质-蛋白质相互作用(PPI)网络图确定了可能影响氮素吸收的八个关键基因(TPIP1、GAPB、HEMB、PGK3、PSBO、PSBP2、PSAG 和 GLN2)。氮吸收、氮同化与氮再动员相结合以及维持光合作用以应对氮缺乏等方面的不利变化导致 TN90 的氮利用效率较低。关键基因(TPIP1、GAPB、PGK3、PSBO、PSBP2、PSAG 和 GLN2)与改善缺氮条件下烟草植株的光合作用和氮代谢有关。
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
Plant Direct
Plant Direct Environmental Science-Ecology
CiteScore
5.00
自引率
3.30%
发文量
101
审稿时长
14 weeks
期刊介绍: Plant Direct is a monthly, sound science journal for the plant sciences that gives prompt and equal consideration to papers reporting work dealing with a variety of subjects. Topics include but are not limited to genetics, biochemistry, development, cell biology, biotic stress, abiotic stress, genomics, phenomics, bioinformatics, physiology, molecular biology, and evolution. A collaborative journal launched by the American Society of Plant Biologists, the Society for Experimental Biology and Wiley, Plant Direct publishes papers submitted directly to the journal as well as those referred from a select group of the societies’ journals.
期刊最新文献
Broad-scale phenotyping in Arabidopsis reveals varied involvement of RNA interference across diverse plant-microbe interactions. Localization of proteins involved in the biogenesis and repair of the photosynthetic apparatus to thylakoid subdomains in Arabidopsis. A strategy for identification and characterization of genic mutations using a temperature-sensitive chlorotic soybean mutant as an example. Interdisciplinarity through internationality: Results from a US-Mexico graduate course bridging computational and plant science. Integrative physiological and transcriptome analysis unravels the mechanism of low nitrogen use efficiency in burley tobacco.
×
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