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硝酸盐还原酶突变体中硝酸盐响应基因的拟表型。

Pseudo-constitutivity of nitrate-responsive genes in nitrate reductase mutants.

机构信息

Fungal Genetics and Genomics Unit, Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Science, University and Research Center, Campus Tulln, 3430 Tulln/Donau, Austria.

出版信息

Fungal Genet Biol. 2013 May;54:34-41. doi: 10.1016/j.fgb.2013.02.003. Epub 2013 Feb 27.

Abstract

In fungi, transcriptional activation of genes involved in NO3(-) assimilation requires the presence of an inducer (nitrate or nitrite) and low intracellular concentrations of the pathway products ammonium or glutamine. In Aspergillus nidulans, the two transcription factors NirA and AreA act synergistically to mediate nitrate/nitrite induction and nitrogen metabolite derepression, respectively. In all studied fungi and in plants, mutants lacking nitrate reductase (NR) activity express nitrate-metabolizing enzymes constitutively without the addition of inducer molecules. Based on their work in A. nidulans, Cove and Pateman proposed an "autoregulation control" model for the synthesis of nitrate metabolizing enzymes in which the functional nitrate reductase molecule would act as co-repressor in the absence and as co-inducer in the presence of nitrate. However, NR mutants could simply show "pseudo-constitutivity" due to induction by nitrate which accumulates over time in NR-deficient strains. Here we examined this possibility using strains which lack flavohemoglobins (fhbs), and are thus unable to generate nitrate internally, in combination with nitrate transporter mutations (nrtA, nrtB) and a GFP-labeled NirA protein. Using different combinations of genotypes we demonstrate that nitrate transporters are functional also in NR null mutants and show that the constitutive phenotype of NR mutants is not due to nitrate accumulation from intracellular sources but depends on the activity of nitrate transporters. However, these transporters are not required for nitrate signaling because addition of external nitrate (10 mM) leads to standard induction of nitrate assimilatory genes in the nitrate transporter double mutants. We finally show that NR does not regulate NirA localization and activity, and thus the autoregulation model, in which NR would act as a co-repressor of NirA in the absence of nitrate, is unlikely to be correct. Results from this study instead suggest that transporter-mediated NO₃⁻ accumulation in NR deficient mutants, originating from traces of nitrate in the media, is responsible for the constitutive expression of NirA-regulated genes, and the associated phenotype is thus termed "pseudo-constitutive".

摘要

在真菌中,参与硝酸盐同化的基因的转录激活需要诱导物(硝酸盐或亚硝酸盐)的存在和途径产物氨或谷氨酰胺的细胞内低浓度。在构巢曲霉中,两个转录因子 NirA 和 AreA 协同作用分别介导硝酸盐/亚硝酸盐诱导和氮代谢物去阻遏。在所有研究过的真菌和植物中,缺乏硝酸还原酶(NR)活性的突变体在没有添加诱导分子的情况下组成型表达硝酸盐代谢酶。基于他们在构巢曲霉中的工作,Cove 和 Pateman 提出了一个“自动调节控制”模型,用于硝酸盐代谢酶的合成,其中功能性硝酸还原酶分子在没有硝酸盐的情况下作为共阻遏物,在有硝酸盐的情况下作为共诱导物。然而,NR 突变体可能只是由于硝酸盐的诱导而表现出“假组成性”,因为在 NR 缺陷型菌株中,硝酸盐会随着时间的推移而积累。在这里,我们使用缺乏黄素血红蛋白(fhbs)的菌株,因此无法在体内产生硝酸盐,结合硝酸盐转运突变体(nrtA、nrtB)和 GFP 标记的 NirA 蛋白,检查了这种可能性。使用不同的基因型组合,我们证明了硝酸盐转运体在 NR 缺失突变体中也具有功能,并表明 NR 突变体的组成型表型不是由于来自细胞内来源的硝酸盐积累,而是取决于硝酸盐转运体的活性。然而,这些转运体不是硝酸盐信号所必需的,因为添加外部硝酸盐(10 mM)会导致硝酸盐转运体双突变体中硝酸盐同化基因的标准诱导。我们最后表明,NR 不调节 NirA 的定位和活性,因此,NR 作为硝酸盐缺乏时 NirA 的共阻遏物的自动调节模型不太可能是正确的。这项研究的结果表明,NR 缺陷突变体中由培养基中痕量硝酸盐引起的转运体介导的 NO₃⁻积累负责 NirA 调节基因的组成型表达,因此相关表型被称为“假组成性”。

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