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硝酸还原酶在多形汉逊酵母硝酸同化途径调控中的作用。

The role of nitrate reductase in the regulation of the nitrate assimilation pathway in the yeast Hansenula polymorpha.

作者信息

Navarro Francisco J, Perdomo Germán, Tejera Paula, Medina Braulio, Machín Félix, Guillén Rosa Maria, Lancha Ana, Siverio José M

机构信息

Departamento de Bioquímica y Biología Molecular, Grupo del Metabolismo del Nitrógeno, Universidad de La Laguna, E-38206 La Laguna, Canarias, Tenerife, Spain.

出版信息

FEMS Yeast Res. 2003 Nov;4(2):149-55. doi: 10.1016/S1567-1356(03)00163-6.

Abstract

The role of nitrate reductase (NR) in the regulation of the nitrate assimilation pathway was evaluated in the yeast Hansenula polymorpha. Posttranscriptional regulation of NR in response to reduced nitrogen sources and the effect of a heterologous NR on the transcriptional regulation of nitrate-assimilatory gene expression was examined. The strain bearing YNR1 (nitrate reductase gene) under the control of the methanol-induced MOX (methanol oxidase) promoter showed that NR is active in the presence of reduced nitrogen sources. In cells incubated with glutamine plus nitrate, rapamycin abolished nitrogen catabolite repression, NR activity being very similar to that in cells induced by nitrate alone. This reveals the involvement of the Tor-signalling pathway in the transcriptional regulation of H. polymorpha nitrate assimilation genes. To assess the role of NR in nitrate-assimilatory gene expression, different strains lacking YNR1, or both YNR1 and YNT1 (high-affinity nitrate transporter) genes, or expressing the tobacco NR under the YNR1 promoter, were used. Tobacco NR abolished the constitutive nitrate-assimilatory gene induction shown by an NR gene disruptant strain. Moreover, in strains lacking the high-affinity nitrate transporter and NR this deregulation disappeared. These facts discard the role of NR protein in the transcriptional induction of the nitrate-assimilatory genes and point out the involvement of the high-affinity nitrate transporter as a part of the nitrate-signalling pathway.

摘要

在多形汉逊酵母中评估了硝酸还原酶(NR)在硝酸同化途径调控中的作用。研究了NR在响应低氮源时的转录后调控以及异源NR对硝酸同化基因表达转录调控的影响。携带受甲醇诱导的MOX(甲醇氧化酶)启动子控制的YNR1(硝酸还原酶基因)的菌株表明,在低氮源存在下NR具有活性。在用谷氨酰胺加硝酸盐培养的细胞中,雷帕霉素消除了氮代谢物阻遏,NR活性与仅由硝酸盐诱导的细胞中的活性非常相似。这揭示了Tor信号通路参与多形汉逊酵母硝酸同化基因的转录调控。为了评估NR在硝酸同化基因表达中的作用,使用了不同的菌株,这些菌株缺乏YNR1,或同时缺乏YNR1和YNT1(高亲和力硝酸盐转运蛋白)基因,或在YNR1启动子下表达烟草NR。烟草NR消除了NR基因破坏菌株所显示的组成型硝酸同化基因诱导。此外,在缺乏高亲和力硝酸盐转运蛋白和NR的菌株中,这种去调控消失了。这些事实排除了NR蛋白在硝酸同化基因转录诱导中的作用,并指出高亲和力硝酸盐转运蛋白作为硝酸信号通路的一部分参与其中。

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