燕麦(Avena sativa L.)关键硝酸盐转运蛋白的综合鉴定和揭示。

IF 3.1 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Rong Cheng, Qiang Xiao, Jie Gong, Renwei Sun, Yinke Du, Wei Zhao, Wei Zheng, Shiqing Gao
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引用次数: 0

摘要

背景:硝酸盐转运蛋白NRT1/PTR家族(NPF)在植物氮吸收和利用中起着至关重要的作用。燕麦(Avena sativa L.)作为重要的六倍体粮食和饲料作物,需要大量的氮素。然而,燕麦硝酸盐转运蛋白1 (NRT1)家族仍未被描述。方法:本研究通过Hmm和Pfam数据库鉴定燕麦NRT1亚家族成员。利用MEGA 11和TBtools软件进行生物信息学分析,以阐明其理化性质、进化关系、染色体定位和基因结构。利用实时定量聚合酶链反应(qRT-PCR)和绿色荧光蛋白(GFP)融合表达载体对候选燕麦NRT1s进行检测。结果:系统发育分类将燕麦nrt1分为8个亚家族,其中以NPF5亚家族数量最多。理化性质分析表明,这些基因编码的蛋白质中氨基酸的数量在235 ~ 673之间,分子量在26 ~ 74 kDa之间。染色体定位表明,这些基因在12条燕麦染色体上分布不均匀。启动子分析显示,光响应元件在这些基因的启动子中出现频率最高(39.3%),其次是脱落酸(ABA)响应元件(13.5%)和茉莉酸甲酯(MeJA)响应元件(9.4%)。qRT-PCR分析显示,大部分基因表现出组织特异性表达模式。其中,AsNPF2.6在低氮(LN)处理后1 h在叶片中高表达,AsNPF4.5在12 h在叶片中高表达,这两个基因在根中均呈现低表达水平。而AsNPF7.16和AsNPF7.19在ln处理后9 h均在根中高表达,而在叶片中低表达。亚细胞定位结果显示,5种蛋白(AsNPF2.6、AsNPF4.5、AsNPF7.16、AsNPF6.8和AsNPF7.19)均定位于细胞质和细胞膜上。结论:我们的研究结果证实了AsNRT1家族成员参与了燕麦氮转运,为进一步研究燕麦nrt1在氮转运中的功能和分子机制提供了理论支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive Identification and Unveiling Key Nitrate-Transporting Proteins in Oat (Avena sativa L.).

Background: Nitrate transporter NRT1/PTR family (NPF) proteins are crucial for plant nitrogen uptake and utilization. As an important hexaploid crop for grain and forage, oat (Avena sativa L.) requires substantial levels of nitrogen. However, the oat nitrate transporter 1 (NRT1) family remains uncharacterized.

Methods: In this study, the oat NRT1 subfamily members were identified through the Hmm and Pfam databases. Bioinformatics analysis was performed using the MEGA 11 and TBtools software to elucidate the physicochemical properties, evolutionary relationships, chromosomal localization, and gene structures. Furthermore, quantitative real-time polymerase chain reaction (qRT-PCR) analysis and the green fluorescent protein (GFP) fusion expression vector were utilized to investigate the candidate oat NRT1s.

Results: Phylogenetic classification categorized oat NRT1s into eight subfamilies, with the most abundant being the NPF5 subfamily. Physicochemical property analysis revealed that the number of amino acids in the proteins encoded by these genes ranged from 235 to 673, with their molecular weights (MWs) ranging from 26 kDa to 74 kDa. Chromosomal localization revealed that these genes were unevenly distributed across all 12 oat chromosomes. Promoter analysis revealed that light-responsive elements appeared most frequently in the promoters of these genes (39.3%), followed by abscisic acid (ABA)-responsive elements (13.5%) and methyl jasmonate (MeJA)-responsive elements (9.4%). qRT-PCR analysis revealed that most of the genes exhibited tissue-specific expression patterns. Among them, AsNPF2.6 was highly expressed in the leaves at 1 h post-low nitrogen (LN) treatment, while AsNPF4.5 was highly expressed in the leaves at 12 h. Both these genes exhibited low expression levels in the roots. However, AsNPF7.16 and AsNPF7.19 were both highly expressed in the roots at 9 h post-LN treatment but exhibited low expression in the leaves. Subcellular localization revealed that all five proteins (AsNPF2.6, AsNPF4.5, AsNPF7.16, AsNPF6.8, and AsNPF7.19) were localized to the cytoplasm and cell membrane.

Conclusions: Our results demostrate the involvement of AsNRT1 family members in nitrogen transport in oat, providing theoretical support for further investigation into the functions and molecular mechanisms of action of oat NRT1s in nitrogen transport.

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