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Distinct Roles of Nitrate and Nitrite in Regulation of Expression of the Nitrate Transport Genes in the Moss Physcomitrella patens

机译:硝酸盐和亚硝酸盐在苔藓小孢子中硝酸盐转运基因表达调控中的不同作用

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Five NRT2 genes and three Nar2 genes, encoding putative high-affinity nitrate transporters, and the respective cDNAs were identified and characterized in Physcomitrella patens. The deduced moss NRT2 and NAR2 proteins were more similar to the corresponding proteins of higher plants than to those of the green alga Chlamydomonas reinhardtii. Expression of all the genes was inhibited by ammonium added to the medium. The regulation by ammonium was abolished by an inhibitor of glutamine synthetase, but the effect of this inhibitor was counteracted by an inhibitor of glutamate synthase. Negative correlation was observed between the glutamine content of protonemata and the transcript levels of PpNRT2 and PpNar2. These results indicated that glutamine is the signal for repression of the genes. All the genes except PpNRT2;5 showed transient expression stimulated by nitrate but not by nitrite, peaking at 2–4 h after the medium was deprived of ammonium. When the glutamine synthetase inhibitor was used to inhibit assimilation of the ammonium generated intracellularly from nitrate or nitrite, the second phase of activation of genes became manifest at ~8 h after the medium was deprived of ammonium. Surprisingly, both nitrate and nitrite stimulated gene expression at this stage. PpNRT2;5 was distinct from the other genes in that its expression is sharply induced by nitrite, is strictly dependent on nitrite or nitrate, and is much less susceptible to the feedback regulation, retaining a constant level in nitrate-containing medium. These results indicated that P. patens has multiple mechanisms for sensing nitrate and nitrite.
机译:在Physcomitrella patens中鉴定并鉴定了5个编码假定的高亲和力硝酸盐转运蛋白的NRT2基因和3个Nar2基因。推导的苔藓NRT2和NAR2蛋白与高等植物的相应蛋白相比,与绿藻莱茵衣藻的蛋白更相似。加入培养基中的铵盐可抑制所有基因的表达。谷氨酰胺合成酶的抑制剂取消了铵的调节,但是谷氨酸合成酶的抑制剂抵消了该抑制剂的作用。质子瘤的谷氨酰胺含量与PpNRT2和PpNar2的转录水平之间存在负相关。这些结果表明,谷氨酰胺是抑制基因的信号。除PpNRT2; 5以外的所有基因均显示出受硝酸盐刺激而不是受亚硝酸盐刺激的瞬时表达,在培养基中缺少铵后2-4 h达到峰值。当使用谷氨酰胺合成酶抑制剂抑制硝酸盐或亚硝酸盐在细胞内产生的铵同化时,在培养基中的铵被剥夺后约8 h,基因激活的第二阶段变得明显。出人意料的是,在此阶段,硝酸盐和亚硝酸盐均可刺激基因表达。 PpNRT2; 5与其他基因的不同之处在于,其表达受到亚硝酸盐的强烈诱导,严格依赖于亚硝酸盐或硝酸盐,并且对反馈调节的敏感性更低,在含硝酸盐的培养基中保持恒定水平。这些结果表明P. patens具有多种感应硝酸盐和亚硝酸盐的机制。

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