A novel transcription factor CsSNACA2 plays a pivotal role within nitrogen assimilation in tea plants

IF 6.2 1区 生物学 Q1 PLANT SCIENCES
Deyuan Jiang, Li Xu, Weiwei Wen
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Abstract

Tea (Camellia sinensis) is a globally renowned economic crop, with organs such as leaves and buds utilized for consumption. As a perennial foliage crop, tea plants have high-nitrogen consumption and demand but exhibit relatively low nitrogen use efficiency. Exploring the genetic factors involved in nitrogen assimilation in tea plants could lead to improvements in both tea yield and quality. Here, we first conducted transcriptome sequencing on two tissues (roots and young leaves) under two different nitrate levels (0.2 and 2.5 mm KNO3) and at six time points (0, 15, and 45 min; 2 and 6 h and 2 days). Differential gene expression patterns were observed for several genes that exhibited altered expression at 2 h. Clustering and enrichment analyses, along with co-expression network construction, provided evidence for the crucial involvement of CsSNACA2 in nitrogen assimilation. CsSNACA2 overexpression elicited pronounced phenotypic changes in nitrogen-deficient plants. Furthermore, CsSNACA2 suppressed the expression of CsNR (encoding nitrate reductase) and CsCLCa (encoding a NO 3 /H+ exchanger). Moreover, CsSNACA2 served as a downstream target of CsSPL6.1. In addition, we characterized Csi-miR156e and Csi-miR156k, which directly cleave CsSPL6.1. This study identified a transcription factor module participating in nitrogen assimilation in tea plants, providing a genetic foundation for future innovations in tea cultivar improvement. These results broaden our understanding of the genetic mechanisms governing nitrogen assimilation in dicotyledonous plants.

一种新的转录因子CsSNACA2在茶树氮素同化中起着关键作用。
茶(Camellia sinensis)是全球知名的经济作物,其叶子和芽等器官用于消费。茶树作为多年生叶作物,氮素消耗和需要量较大,但氮素利用效率相对较低。探索与茶树氮素同化有关的遗传因素,有助于提高茶叶产量和品质。在这里,我们首先对两种不同硝酸盐水平(0.2和2.5 mm KNO3)下的两个组织(根和幼叶)在6个时间点(0,15和45分钟)进行转录组测序;2、6小时和2天)。不同的基因表达模式被观察到在2小时表现出表达改变的几个基因。聚类和富集分析以及共表达网络的构建为CsSNACA2参与氮同化提供了重要证据。CsSNACA2过表达在缺氮植株中引起显著的表型变化。此外,CsSNACA2抑制了编码硝酸还原酶的CsNR和编码NO 3 - $$ {\mathrm{NO}}_3^{-} $$ /H+交换剂的CsCLCa的表达。此外,CsSNACA2是CsSPL6.1的下游靶点。此外,我们还表征了直接切割CsSPL6.1的Csi-miR156e和Csi-miR156k。本研究鉴定出一个参与茶树氮素同化的转录因子模块,为今后茶树品种改良创新提供遗传基础。这些结果拓宽了我们对双子叶植物氮素同化遗传机制的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
The Plant Journal
The Plant Journal 生物-植物科学
CiteScore
13.10
自引率
4.20%
发文量
415
审稿时长
2.3 months
期刊介绍: Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community. Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.
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