Zhang Shuang, Cao Lina, Sun Xue, Yu Jiajie, Xu Xiuyue, Chang Ruhui, Suo Juanfang, Liu Guanjun, Xu Zhiru, Qu Chunpu
Ministry of Education, Key Laboratory of Saline-Alkali Vegetation Ecology Restoration (Northeast Forestry University), Harbin, 150040 People's Republic of China.
College of Life Science, Northeast Forestry University, Harbin, 150040 People's Republic of China.
3 Biotech. 2021 Mar;11(3):149. doi: 10.1007/s13205-021-02697-9. Epub 2021 Feb 27.
Plant UDP-glucose 6-dehydrogenase (UGDH) is an important enzyme for the formation of hemicellulose and pectin. Previous studies on UGDH have primarily focused on the biosynthesis of cell wall polysaccharides, while few studies have focused on their regulation by exogenous nitrogen. In the present study, four genes encoding PtUGDH proteins were analyzed by bioinformatics methods. And, the expression profiles of genes under different nitrogen treatments were evaluated with qRT-PCR. The results showed that PtUGDHs have conserved NAD coenzyme binding motif GAGYVGG and the catalytic motif GFGGSCFQKDIL. According to the phylogenetic analysis, PtUGDHs were divided into two subgroups. PtUGDH3 and PtUGDH4 were closely related to AtUGDH1 (important for normal development of cell wall structure) Chromosomal distribution and genome synteny analysis revealed four segmental-duplicated gene pairs on chr4, 8, 10 and 17. Tissue-specific data from PlantGenIE showed that and were highly expressed in stems. The qRT-PCR detection showed that the expression of 3 in the lower stem and 2 of upper leaves were significantly increased induced by low ammonium or nitrate condition. This comprehensive analysis of the family in poplar provides new insights into their regulation by nitrogen, and would increase our understanding of the roles of UGDHs in hemicellulose and pectin biosynthesis in the cell wall and during poplar development.
The online version contains supplementary material available at 10.1007/s13205-021-02697-9.
植物UDP - 葡萄糖6 - 脱氢酶(UGDH)是半纤维素和果胶形成的重要酶。以往对UGDH的研究主要集中在细胞壁多糖的生物合成上,而很少有研究关注其受外源氮的调控。在本研究中,通过生物信息学方法分析了四个编码PtUGDH蛋白的基因。并且,用qRT - PCR评估了不同氮处理下这些基因的表达谱。结果表明,PtUGDHs具有保守的NAD辅酶结合基序GAGYVGG和催化基序GFGGSCFQKDIL。根据系统发育分析,PtUGDHs分为两个亚组。PtUGDH3和PtUGDH4与AtUGDH1密切相关(对细胞壁结构的正常发育很重要)。染色体分布和基因组共线性分析揭示了在chr4、8、10和17上有四对片段重复基因对。来自PlantGenIE的组织特异性数据显示,[此处原文缺失相关基因名称]在茎中高表达。qRT - PCR检测表明,低铵或硝酸盐条件诱导下,下茎中的3和上叶中的2的表达显著增加。对杨树中该基因家族的这种综合分析为氮对其的调控提供了新的见解,并将增加我们对UGDHs在细胞壁半纤维素和果胶生物合成以及杨树发育过程中作用的理解。
在线版本包含可在10.1007/s13205 - 021 - 02697 - 9获取的补充材料。