亚硝酸盐还原酶
液泡
硝酸还原酶
腿血红蛋白
生物化学
生物
亚硝酸盐
基因表达
一氧化氮
突变体
化学
硝酸盐
还原酶
分子生物学
细胞生物学
氮同化
丙酮酸脱氢酶复合物
基因表达调控
结核(地质)
谷氨酸脱氢酶
环己酰亚胺
二氢脂酰胺脱氢酶
醇脱氢酶
甘氨酸裂解系统
血红素
根瘤
抄写(语言学)
转录因子
作者
Suyu Jiang,Jin‐Peng Gao,Yiting Ruan,Wenjie Liang,Yi-Sheng Wang,Herong Niu,Rosa M Esquinas-Ariza,Jian Zhang,Manuel Becana,Ping Xu,Jeremy D. Murray
标识
DOI:10.1093/plphys/kiaf514
摘要
Abstract The NIN-like protein 2 (NLP2) transcription factor is highly expressed in the infected cells of the N2 fixation zone of mature nodules in Medicago truncatula. In these cells, NLP2 directly activates the expression of leghemoglobin genes and is required for the full expression of nitrite reductase (NiR). Histological examination of nodules formed under different nitrate regimes revealed that the infected cells of nlp2 display abnormal vacuole morphology under high nitrate (5 mm KNO3). This phenotype is associated with starch accumulation, higher expression of starch biosynthesis genes, and increased levels of nitrite and nitric oxide. A transcriptomic comparison of nlp2 and wild-type nodules across nitrate concentrations revealed that under high nitrate, nlp2 shows lower expression of genes important for hypoxia adaptation, such as alcohol dehydrogenase and pyruvate decarboxylase (PDC), and increased expression of S-nitrosoglutathione reductase (GSNOR), which encodes a key enzyme for nitric oxide homeostasis. These changes in gene expression were associated with lower nodule ATP levels and a higher NAD+/NADH ratio, suggesting that energy metabolism is specifically compromised in nlp2 nodules under high nitrate. Transgenic expression of NiR in the nodules of nlp2-1 mutants grown under high nitrate rescued the vacuole phenotype and restored the expression of GSNOR and PDC to normal levels. Overall, our data indicate a role for NLP2 in the regulation of NiR in N2-fixing cells, suggesting a role for nitrate reduction in nodule energy homeostasis.
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