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藤仓镰孢中GATA转录因子AreA(全局氮调节因子)和AreB之间的相互作用。

The interplay between the GATA transcription factors AreA, the global nitrogen regulator and AreB in Fusarium fujikuroi.

作者信息

Michielse C B, Pfannmüller A, Macios M, Rengers P, Dzikowska A, Tudzynski B

机构信息

Institute of Biology and Biotechnology of Plants, Westfälische Wilhelms-University, Schlossplatz 8, 48143, Münster, Germany.

出版信息

Mol Microbiol. 2014 Feb;91(3):472-93. doi: 10.1111/mmi.12472. Epub 2013 Dec 19.

Abstract

Nitrogen metabolite repression (NMR) in filamentous fungi is controlled by the GATA transcription factors AreA and AreB. While AreA mainly acts as a positive regulator of NMR-sensitive genes, the role of AreB is not well understood. We report the characterization of AreB and its interplay with AreA in the gibberellin-producing fungus Fusarium fujikuroi. The areB locus produces three different transcripts that each code for functional proteins fully complementing the areB deletion mutant that influence growth and secondary metabolism. However, under nitrogen repression, the AreB isoforms differ in subcellular localization indicating distinct functions under these conditions. In addition, AreA and two isoforms of AreB colocalize in the nucleus under low nitrogen, but their nuclear localization disappears under conditions of high nitrogen. Using a bimolecular fluorescence complementation (BiFC) approach we showed for the first time that one of the AreB isoforms interacts with AreA when starved of nitrogen. Cross-species complementation revealed that some AreB functions are retained between F. fujikuroi and Aspergillus nidulans while others have diverged. By comparison to other fungi where AreB was postulated to function as a negative counterpart of AreA, AreB can act as both repressor and activator of transcription in F. fujikuroi.

摘要

丝状真菌中的氮代谢物阻遏(NMR)由GATA转录因子AreA和AreB控制。虽然AreA主要作为NMR敏感基因的正调控因子,但AreB的作用尚不清楚。我们报道了在产赤霉素的藤仓镰孢菌中AreB的特性及其与AreA的相互作用。areB基因座产生三种不同的转录本,每个转录本编码的功能蛋白都能完全互补影响生长和次级代谢的areB缺失突变体。然而,在氮阻遏条件下,AreB同工型在亚细胞定位上有所不同,表明在这些条件下具有不同的功能。此外,在低氮条件下,AreA和两种AreB同工型共定位于细胞核,但在高氮条件下它们的核定位消失。我们首次使用双分子荧光互补(BiFC)方法表明,在氮饥饿时,一种AreB同工型与AreA相互作用。跨物种互补表明,藤仓镰孢菌和构巢曲霉之间保留了一些AreB功能,而其他功能则发生了分化。与其他假定AreB作为AreA负对应物的真菌相比,AreB在藤仓镰孢菌中既可以作为转录抑制因子,也可以作为转录激活因子。

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