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剖析构巢曲霉硝酸盐簇中氮转录因子协同作用的各个步骤。

Dissecting individual steps of nitrogen transcription factor cooperation in the Aspergillus nidulans nitrate cluster.

作者信息

Berger Harald, Basheer Asjad, Böck Sandra, Reyes-Dominguez Yazmid, Dalik Thomas, Altmann Friedrich, Strauss Joseph

机构信息

Fungal Genomics Unit, Austrian Research Centers, Tech Gate Vienna, Donau-City-Strasse 1, 1220 Vienna, Austria.

出版信息

Mol Microbiol. 2008 Sep;69(6):1385-98. doi: 10.1111/j.1365-2958.2008.06359.x. Epub 2008 Jul 20.

DOI:10.1111/j.1365-2958.2008.06359.x
PMID:18673441
Abstract

In the ascomycete fungus Aspergillus nidulans, the transcriptional activation of nitrate assimilating genes (niiA, niaD) depends on the cooperativity between a general nitrogen status-sensing regulator (the GATA factor AreA) and a pathway-specific activator (the Zn-cluster regulator NirA). Because nitrate assimilation leads to intracellular ammonium formation, it is difficult to determine the individual contributions of NirA and AreA in this complex activation/inactivation process. In an attempt to find a suitable marker for the nitrogen status sensed by AreA, we determined the intracellular free amino acid levels on different nitrogen growth conditions. We show that the amount of glutamine (Gln) inversely correlates with all known AreA activities. We find that AreA mediates chromatin remodelling by increasing histone H3 acetylation, a process triggered by transcriptional activation and, independently of transcription, by nitrogen starvation. NirA also participates in the chromatin opening process during nitrate induction but its function is not related to histone acetylation. This chromatin remodelling function of NirA is dispensable only in nitrogen-starved cells, conditions that lead to elevated AreA chromatin occupancy and histone H3 hyperacetylation. Continuous nitrate assimilation leads to self-nitrogen metabolite repression but nitrate-activated NirA is partially compensating for lowered AreA activities under these conditions.

摘要

在子囊菌烟曲霉中,硝酸盐同化基因(niiA、niaD)的转录激活取决于一种通用的氮状态感应调节因子(GATA因子AreA)和一种途径特异性激活因子(锌簇调节因子NirA)之间的协同作用。由于硝酸盐同化会导致细胞内铵的形成,因此很难确定NirA和AreA在这个复杂的激活/失活过程中的各自贡献。为了找到一个适合AreA所感应的氮状态的标记物,我们测定了在不同氮生长条件下细胞内游离氨基酸的水平。我们发现谷氨酰胺(Gln)的量与所有已知的AreA活性呈负相关。我们发现AreA通过增加组蛋白H3乙酰化来介导染色质重塑,这一过程由转录激活触发,并且在转录独立的情况下由氮饥饿触发。NirA在硝酸盐诱导过程中也参与染色质开放过程,但其功能与组蛋白乙酰化无关。NirA的这种染色质重塑功能仅在氮饥饿细胞中是可有可无的,在这些条件下会导致AreA染色质占有率升高和组蛋白H3过度乙酰化。持续的硝酸盐同化会导致自氮代谢物阻遏,但在这些条件下,硝酸盐激活的NirA部分补偿了降低的AreA活性。

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