Li Da, Jin Ya, Lu Qin-Hua, Ren Ning, Wang Ying-Qi, Li Qing-Sheng
Institute of Sericulture and Tea, Zhejiang Academy of Agricultural Sciences, Hangzhou, 310021, China.
Institute of Sericulture and Tea, Zhejiang Academy of Agricultural Sciences, Hangzhou, 310021, China; College of Horticulture Science, Zhejiang A&F University, Hangzhou, 311300, China.
Plant Physiol Biochem. 2024 Feb;207:108340. doi: 10.1016/j.plaphy.2024.108340. Epub 2024 Jan 5.
NIN-like proteins (NLPs) are evolutionarily conserved transcription factors that are unique to plants and play a pivotal role in responses to nitrate uptake and assimilation. However, a comprehensive analysis of NLP members in tea plants is lacking. The present study performed a genome-wide analysis and identified 33 NLP gene family members of Camellia sinensis that were distributed unequally across 5 chromosomes. Subcellular localisation predictions revealed that all CsNLP proteins were localised in the nucleus. Conservative domain analysis revealed that all of these proteins contained conserved RWP-RK and PB1 domains. Phylogenetic analysis grouped the CsNLP gene family into four clusters. The promoter regions of CsNLPs harboured cis-acting elements associated with plant hormones and abiotic stress responses. Expression profile analysis demonstrated that CsNLP8 was significantly upregulated in roots under nitrate stress conditions. Subcellular localisation analysis found CsNLP8 localised to the nucleus. Dual-luciferase reporter assay demonstrated that CsNLP8 positively regulated the expression of a nitrate transporter gene (CsNRT2.2). These findings provide a comprehensive characterisation of NLP genes in Camellia sinensis and offer insights into the biological function of CsNLP8 in regulating the response to nitrate-induced stress.
NIN 样蛋白(NLPs)是植物特有的、在进化上保守的转录因子,在硝酸盐吸收和同化反应中起关键作用。然而,目前缺乏对茶树中 NLP 成员的全面分析。本研究进行了全基因组分析,鉴定出茶树中 33 个 NLP 基因家族成员,它们不均匀地分布在 5 条染色体上。亚细胞定位预测显示,所有 CsNLP 蛋白都定位于细胞核。保守结构域分析表明,所有这些蛋白都含有保守的 RWP-RK 和 PB1 结构域。系统发育分析将 CsNLP 基因家族分为四个簇。CsNLPs 的启动子区域含有与植物激素和非生物胁迫反应相关的顺式作用元件。表达谱分析表明,在硝酸盐胁迫条件下,CsNLP8 在根中显著上调。亚细胞定位分析发现 CsNLP8 定位于细胞核。双荧光素酶报告基因检测表明,CsNLP8 正向调控硝酸盐转运蛋白基因(CsNRT2.2)的表达。这些发现全面表征了茶树中的 NLP 基因,并为 CsNLP8 在调节硝酸盐诱导胁迫反应中的生物学功能提供了见解。