通过转录谱分析和DNA亲和纯化测序揭示了真菌磷酸盐饥饿反应的一种新的调节因子。

IF 4.7 1区 生物学 Q1 MICROBIOLOGY
mBio Pub Date : 2025-10-08 Epub Date: 2025-08-25 DOI:10.1128/mbio.02023-25
Lori B Huberman, Vincent W Wu, David J Kowbel, Juna Lee, Chris Daum, Vasanth R Singan, Igor V Grigoriev, Ronan C O'Malley, N Louise Glass
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引用次数: 0

摘要

细胞必须准确地感知和反应营养,以竞争资源和建立生长。磷酸盐是信号传导、能量代谢、核酸、磷脂和细胞代谢物合成所必需的关键营养来源。在磷酸盐限制期间,真菌从环境中进口磷酸盐,并从细胞中的含磷酸盐分子中释放磷酸盐。在模式丝状真菌粗神经孢子菌(Neurospora crassa)中,磷酸盐饥饿反应是由保守转录因子nuc1调控的。当磷酸盐充足时,细胞周期蛋白依赖性激酶MDK-1和细胞周期蛋白PREG的复合物抑制了NUC-1的活性。当磷酸盐受限时,MDK-1/PREG对nuc1的抑制被周期蛋白依赖性激酶抑制剂nuc2缓解。我们研究了氮草对磷酸盐饥饿的全球响应。在磷酸盐饥饿期间,NUC-1直接激活编码磷酸酶、核酸酶和磷酸盐转运蛋白的基因表达,并直接抑制与核糖体相关的基因。此外,NUC-1间接激活了一种未表征的转录因子的表达,我们将其命名为nuc-3。在长时间的磷酸盐饥饿后,NUC-3直接抑制参与磷酸盐获取和释放的基因的表达。此外,nuc3直接抑制细胞周期蛋白依赖性激酶抑制剂nuc2的表达。因此,通过NUC-3直接抑制磷酸盐饥饿反应的基因和nuc-2(磷酸盐饥饿反应的激活因子)的结合,NUC-3可以在长时间的磷酸盐饥饿后起到抑制磷酸盐饥饿反应的作用。这种制动机制可以减少转录,一个磷酸盐密集的过程,在延长磷酸盐限制的条件下。真菌已经进化出了对可用营养物质作出反应的调节网络。磷酸盐通常是真菌的限制性营养素,对许多细胞功能至关重要,包括核酸和磷脂生物合成,细胞信号传导和能量代谢。真菌对磷酸盐限制的反应在与植物和动物的相互作用中是重要的。我们研究了模式丝状真菌粗神经孢子菌(Neurospora crassa)对磷酸盐饥饿的全球转录反应和主要转录调节因子nuc1的作用。我们的数据表明,NUC-1是一种双功能转录因子,它直接激活磷酸盐获取基因,同时直接抑制与磷酸盐密集过程相关的基因。NUC-1间接调控一个未知的转录因子,我们将其命名为nuc-3。在长时间的磷酸盐饥饿中,NUC-3直接抑制磷酸盐获取基因和nuc-2,后者是磷酸盐饥饿反应的激活因子。因此,当磷酸盐饥饿持续存在时,NUC-3可作为磷酸盐饥饿反应的制动器,以减少磷酸盐密集型活动,如转录激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel regulator of the fungal phosphate starvation response revealed by transcriptional profiling and DNA affinity purification sequencing.

Cells must accurately sense and respond to nutrients to compete for resources and establish growth. Phosphate is a critical nutrient source necessary for signaling, energy metabolism, and synthesis of nucleic acids, phospholipids, and cellular metabolites. During phosphate limitation, fungi import phosphate from the environment and liberate phosphate from phosphate-containing molecules in the cell. In the model filamentous fungus Neurospora crassa, the phosphate starvation response is regulated by the conserved transcription factor NUC-1. The activity of NUC-1 is repressed by a complex of the cyclin-dependent kinase MDK-1 and the cyclin PREG when phosphate is plentiful. When phosphate is limiting, NUC-1 repression by MDK-1/PREG is relieved by the cyclin-dependent kinase inhibitor NUC-2. We investigated the global response of N. crassa to phosphate starvation. During phosphate starvation, NUC-1 directly activated the expression of genes encoding phosphatases, nucleases, and a phosphate transporter and directly repressed genes associated with the ribosome. Additionally, NUC-1 indirectly activated the expression of an uncharacterized transcription factor, which we named nuc-3. NUC-3 directly repressed the expression of genes involved in phosphate acquisition and liberation after an extended period of phosphate starvation. Additionally, NUC-3 directly repressed the expression of the cyclin-dependent kinase inhibitor nuc-2. Thus, through the combination of NUC-3 direct repression of genes in the phosphate starvation response and nuc-2, an activator of the phosphate starvation response, NUC-3 serves to act as a brake on the phosphate starvation response after an extended period of phosphate starvation. This braking mechanism could reduce transcription, a phosphate-intensive process, under conditions of extended phosphate limitation.IMPORTANCEFungi have evolved regulatory networks to respond to available nutrients. Phosphate is often a limiting nutrient for fungi that is critical for many cellular functions, including nucleic acid and phospholipid biosynthesis, cell signaling, and energy metabolism. The fungal response to phosphate limitation is important in interactions with plants and animals. We investigated the global transcriptional response to phosphate starvation and the role of a major transcriptional regulator, NUC-1, in the model filamentous fungus Neurospora crassa. Our data show that NUC-1 is a bifunctional transcription factor that directly activates phosphate acquisition genes, while directly repressing genes associated with phosphate-intensive processes. NUC-1 indirectly regulates an uncharacterized transcription factor, which we named nuc-3. NUC-3 directly represses phosphate acquisition genes and nuc-2, an activator of the phosphate starvation response, during extended periods of phosphate starvation. Thus, NUC-3 acts as a brake on the phosphate starvation response to reduce phosphate-intensive activities, like transcriptional activation, when phosphate starvation persists.

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来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
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