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Nitrogen Signaling Factor Impact on Gene Expression in Yeast


Основні поняття
The author argues that NSF triggers a change from fermentation to respiration-like gene expression, impacting adaptive growth in S. pombe by interacting with mitochondrial sulfide:quinone oxidoreductase Hmt2.
Анотація

Microbes like S. pombe use NSF as a signal to adapt to changing nutrient conditions, bypassing nitrogen catabolite repression (NCR) and promoting growth. NSF induces a shift from fermentation to respiration-like gene expression, enhancing the uptake of branched-chain amino acids (BCAA) under high ammonium conditions. The study identifies Hmt2 as a direct target of NSF, linking mitochondrial respiration to adaptive growth.

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Статистика
"Our results suggest that NSF activity is not restricted to nitrogen metabolism alone." "An intra-species chemical communication system regulates NCR in Schizosaccharomyces pombe." "Synthetic NSFs are sufficient to bypass NCR and promote growth under high-quality nitrogen sources."
Цитати
"The pathways and mechanisms by which NSF acts are poorly understood." "NSF is part of a species-specific communication system enabling cells adapting to changing nutritional conditions."

Ключові висновки, отримані з

by Buehler,M., ... о www.biorxiv.org 12-19-2023

https://www.biorxiv.org/content/10.1101/2023.12.18.572203v1
Nitrogen signaling factor triggers a respiration-like gene expression program

Глибші Запити

How does the interaction between NSF and Hmt2 impact the overall metabolic response of S. pombe

The interaction between NSF and Hmt2 plays a crucial role in shaping the metabolic response of S. pombe. Hmt2, as a sulfide:quinone oxidoreductase located in the mitochondria, is involved in electron transport chain activities by accepting electrons from hydrogen sulfide and transferring them to quinones. This process contributes to mitochondrial respiration and energy production within the cell. When NSF interacts with Hmt2, it triggers changes that enhance respiratory activity, leading to an increase in oxygen consumption rates and promoting a shift towards a respiration-like gene expression program. This interaction influences the overall metabolic response by facilitating adaptive growth under high ammonium conditions through enhanced mitochondrial respiration. By activating Hmt2 via NSF signaling, cells can better cope with nutrient limitations or changing environmental conditions by optimizing their energy production pathways. The increased respiratory capacity allows for efficient utilization of available nutrients and supports cellular functions necessary for growth and survival.

What implications could the findings have for understanding microbial communication systems beyond yeast

The findings regarding NSF-mediated communication mechanisms in S. pombe have broader implications for understanding microbial communication systems beyond yeast species. The identification of NSF as a diffusible signal that modulates gene expression programs highlights the importance of chemical signaling in coordinating responses at the population level among microorganisms. Understanding how external factors like metabolites or chemicals influence transcriptional networks provides insights into how microbes adapt to varying environmental cues collectively rather than individually. This knowledge could be applied to studying interspecies interactions, biofilm formation dynamics, virulence regulation in pathogens, or even industrial applications where microbial communities are utilized for bioprocessing purposes. By unraveling the molecular mechanisms underlying cell-to-cell communication mediated by signals like NSF, researchers can uncover fundamental principles governing microbial behavior and potentially discover novel strategies for manipulating these processes beneficially across different contexts.

How might the discovery of Ayr1's role in metabolizing NSF influence future research on cell-to-cell signaling mechanisms

The discovery of Ayr1's role in metabolizing NSF introduces new dimensions to our understanding of cell-to-cell signaling mechanisms and their regulatory networks. Ayr1's function as an enzyme involved in lipid metabolism suggests that it may play a critical role in regulating the availability or activity of NSF within cells. This finding opens up avenues for further research on how metabolic enzymes interact with signaling molecules like NSF to modulate cellular responses dynamically. Investigating how Ayr1 influences the levels or stability of NSF could provide valuable insights into feedback loops controlling signal transduction pathways linked to nutrient sensing or stress responses. Moreover, exploring Ayr1's impact on downstream effects triggered by NSF signaling could reveal intricate connections between metabolic processes and genetic regulation mediated by extracellular signals. Understanding how Ayr1 affects adaptive growth responses initiated by NSA may lead to novel strategies for manipulating cellular behaviors through targeted modulation of key metabolic enzymes involved in signal processing pathways.
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