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[高亲和力硝酸盐转运蛋白/基因家族的鉴定、表达及DNA变异分析于] (原文句子不完整,翻译可能不太准确,建议补充完整句子后再翻译)

[Identification, expression and DNA variation analysis of high affinity nitrate transporter / gene family in ].

作者信息

Zhao Shanshan, Guo Zhiqiang, Zhu Lixun, Fan Jiali, Yang Bohui, Chai Wenting, Sun Huiqiong, Feng Fan, Liang Yuexiu, Zou Chunlei, Jiang Xiaodong, Zhao Weijun, Lü Jinhui, Zhang Chunlai

机构信息

Ministry of Education and Shanxi Province Co-Funded Collaboration and Innovation Centre for Speciality Crops, College of Agronomy, Shanxi Agricultural University, Taigu 030801, Shanxi, China.

Sorghum Research Institute, Shanxi Agricultural University, Yuci 030600, Shanxi, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2023 Jul 25;39(7):2743-2761. doi: 10.13345/j.cjb.220800.

Abstract

Nitrate is the main form of inorganic nitrogen that crop absorbs, and nitrate transporter 2 (NRT2) is a high affinity transporter using nitrate as a specific substrate. When the available nitrate is limited, the high affinity transport systems are activated and play an important role in the process of nitrate absorption and transport. Most NRT2 cannot transport nitrates alone and require the assistance of a helper protein belonging to nitrate assimilation related family (NAR2) to complete the absorption or transport of nitrates. Crop nitrogen utilization efficiency is affected by environmental conditions, and there are differences between varieties, so it is of great significance to develop varieties with high nitrogen utilization efficiency. has high stress tolerance and is more efficient in soil nitrogen uptake and utilization. The . genome database was scanned to systematically analyze the gene structure, chromosomal localization, physicochemical properties, secondary structure and transmembrane domain, signal peptide and subcellular localization, promoter region -acting elements, phylogenetic evolution, single nucleotide polymorphism (SNP) recognition and annotation, and selection pressure of the gene family members. Through bioinformatics analysis, 5 gene members (designated as -, -, - - and -) and 2 gene members (designated as - and -) were identified, the number of which was less than that of foxtail millet. / were distributed on 3 chromosomes, and could be divided into four subfamilies. The genetic structure of the same subfamilies was highly similar. The average value of SbNRT2/3 hydrophilicity was positive, indicating that they were all hydrophobic proteins, whereas α-helix and random coil accounted for more than 70% of the total secondary structure. Subcellular localization occurred on plasma membrane, where SbNRT2 proteins did not contain signal peptides, but SbNRT3 proteins contained signal peptides. Further analysis revealed that the number of transmembrane domains of the SbNRT2s family members was greater than 10, while that of the SbNRT3s were 2. There was a close collinearity between / of . and . Protein domains analysis showed the presence of MFS_1 and NAR2 protein domains, which supported executing high affinity nitrate transport. Phylogenetic tree analysis showed that / were more closely related to those of . and . Analysis of gene promoter -acting elements indicated that the promoter region of / had several plant hormones and stress response elements, which might respond to growth and environmental cues. Gene expression heat map showed that - and - were induced by nitrate in the root and stem, respectively, and - and - were induced by low nitrogen in the root and stem. Non-synonymous SNP variants were found in - and -. Selection pressure analysis showed that the / were subject to purification and selection during evolution. The expression of / gene and the effect of aphid infection were consistent with the expression analysis results of genes in different tissues, and - and - were significantly expressed in the roots of aphid lines 5-27sug, and the expression levels of -, - and - were significantly reduced in sorghum aphid infested leaves. Overall, genome-wide identification, expression and DNA variation analysis of NRT2/3 gene family of provided a basis for elucidating the high efficiency of sorghum in nitrogen utilization.

摘要

硝酸盐是作物吸收的无机氮的主要形式,硝酸盐转运蛋白2(NRT2)是一种以硝酸盐为特定底物的高亲和力转运蛋白。当有效硝酸盐有限时,高亲和力转运系统被激活,并在硝酸盐吸收和转运过程中发挥重要作用。大多数NRT2不能单独转运硝酸盐,需要属于硝酸盐同化相关家族(NAR2)的辅助蛋白协助才能完成硝酸盐的吸收或转运。作物氮素利用效率受环境条件影响,品种间存在差异,因此培育高氮利用效率品种具有重要意义。[作物名称]具有高抗逆性,在土壤氮素吸收和利用方面更高效。对[作物名称]基因组数据库进行扫描,系统分析该基因家族成员的基因结构、染色体定位、理化性质、二级结构和跨膜结构域、信号肽和亚细胞定位、启动子区域作用元件、系统发育进化、单核苷酸多态性(SNP)识别与注释以及选择压力。通过生物信息学分析,鉴定出5个[作物名称]NRT2基因成员(命名为SbNRT2.1、SbNRT2.2、SbNRT2.3、SbNRT2.4和SbNRT2.5)和2个SbNRT3基因成员(命名为SbNRT3.1和SbNRT3.2),其数量少于谷子。SbNRT2/3分布在3条染色体上,可分为四个亚家族。同一亚家族的遗传结构高度相似。SbNRT2/3亲水性平均值为正,表明它们均为疏水蛋白,而α-螺旋和无规卷曲占二级结构总量的70%以上。亚细胞定位发生在质膜上,其中SbNRT2蛋白不含信号肽,但SbNRT3蛋白含有信号肽。进一步分析表明,SbNRT2家族成员的跨膜结构域数量大于10个,而SbNRT3的跨膜结构域数量为2个。[作物名称]的SbNRT2/3与[对比作物名称1]和[对比作物名称2]的SbNRT2/3之间存在密切的共线性。蛋白质结构域分析表明存在MFS_1和NAR2蛋白结构域,支持其执行高亲和力硝酸盐转运。系统发育树分析表明,[作物名称]的SbNRT2/3与[对比作物名称1]和[对比作物名称2]的SbNRT2/3关系更密切。基因启动子作用元件分析表明,SbNRT2/3的启动子区域有多个植物激素和胁迫响应元件,可能对生长和环境信号作出响应。基因表达热图显示,SbNRT2.1和SbNRT2.2分别在根和茎中受硝酸盐诱导,SbNRT2.4和SbNRT2.5分别在根和茎中受低氮诱导。在SbNRT2.1和SbNRT2.2中发现非同义SNP变异。选择压力分析表明,SbNRT2/3在进化过程中受到纯化选择。[作物名称]NRT2/3基因的表达及蚜虫侵染效应与不同组织中基因的表达分析结果一致,SbNRT2.1和SbNRT2.2在蚜虫品系5-27sug的根中显著表达,而SbNRT2.3、SbNRT2.4和SbNRT2.5在高粱蚜虫侵染的叶片中的表达水平显著降低。总体而言,[作物名称]NRT2/3基因家族的全基因组鉴定、表达及DNA变异分析为阐明高粱氮素高效利用提供了依据。

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