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鉴定受 G 蛋白偶联受体 GprB 和 GprD 影响的 Aspergillus nidulans 代谢途径。

Identification of metabolic pathways influenced by the G-protein coupled receptors GprB and GprD in Aspergillus nidulans.

机构信息

Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, São Paulo, Brazil.

出版信息

PLoS One. 2013 May 1;8(5):e62088. doi: 10.1371/journal.pone.0062088. Print 2013.

Abstract

Heterotrimeric G-protein-mediated signaling pathways play a pivotal role in transmembrane signaling in eukaryotes. Our main aim was to identify signaling pathways regulated by A. nidulans GprB and GprD G-protein coupled receptors (GPCRs). When these two null mutant strains were compared to the wild-type strain, the ΔgprB mutant showed an increased protein kinase A (PKA) activity while growing in glucose 1% and during starvation. In contrast, the ΔgprD has a much lower PKA activity upon starvation. Transcriptomics and (1)H NMR-based metabolomics were performed on two single null mutants grown on glucose. We noted modulation in the expression of 11 secondary metabolism gene clusters when the ΔgprB and ΔgprD mutant strains were grown in 1% glucose. Several members of the sterigmatocystin-aflatoxin gene cluster presented down-regulation in both mutant strains. The genes of the NR-PKS monodictyphenone biosynthesis cluster had overall increased mRNA accumulation in ΔgprB, while in the ΔgprD mutant strain the genes had decreased mRNA accumulation. Principal component analysis of the metabolomic data demonstrated that there was a significant metabolite shift in the ΔgprD strain. The (1)H NMR analysis revealed significant expression of essential amino acids with elevated levels in the ΔgprD strain, compared to the wild-type and ΔgprB strains. With the results, we demonstrated the differential expression of a variety of genes related mainly to secondary metabolism, sexual development, stress signaling, and amino acid metabolism. We propose that the absence of GPCRs triggered stress responses at the genetic level. The data suggested an intimate relationship among different G-protein coupled receptors, fine-tune regulation of secondary and amino acid metabolisms, and fungal development.

摘要

三聚体 G 蛋白介导的信号通路在真核生物的跨膜信号转导中发挥着关键作用。我们的主要目的是鉴定受曲霉属 GprB 和 GprD G 蛋白偶联受体 (GPCR) 调节的信号通路。当比较这两个缺失突变株与野生型菌株时,ΔgprB 突变体在 1%葡萄糖中生长和饥饿时表现出增加的蛋白激酶 A (PKA) 活性。相比之下,ΔgprD 在饥饿时 PKA 活性低得多。对在葡萄糖上生长的两个单缺失突变体进行了转录组学和基于 (1)H NMR 的代谢组学分析。当 ΔgprB 和 ΔgprD 突变菌株在 1%葡萄糖中生长时,我们注意到 11 个次级代谢基因簇的表达发生了调制。在两个突变菌株中,均下调了几株棒曲霉素-黄曲霉毒素基因簇的基因。NR-PKS 单二肽酚生物合成簇的基因在 ΔgprB 中总体上 mRNA 积累增加,而在 ΔgprD 突变菌株中基因的 mRNA 积累减少。代谢组学数据的主成分分析表明,ΔgprD 菌株的代谢物发生了显著变化。(1)H NMR 分析表明,与野生型和 ΔgprB 菌株相比,ΔgprD 菌株中必需氨基酸的表达显著增加,且水平升高。根据这些结果,我们证明了与次级代谢、有性发育、应激信号和氨基酸代谢等相关的多种基因的差异表达。我们提出,缺乏 GPCR 会在遗传水平上引发应激反应。数据表明不同 G 蛋白偶联受体之间存在密切关系,可精细调节次级代谢物和氨基酸代谢以及真菌发育。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a178/3641053/9ec401c46190/pone.0062088.g001.jpg

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