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Published on: March 5, 2019
The Pneumocystis meiotic PCRan1p kinase exhibits unique temperature-regulated activity
Joshua W Burgess1, Theodore J Kottom, Leah R Villegas
1Thoracic Disease Research Unit, 8-24 Stabile Building, Mayo Clinic, 200 1st Street SW, Rochester, MN 55905, USA.
Abstract:
Pneumocystis organisms are opportunistic fungal pathogens that cause significant pneumonia in immune-compromised hosts. Recent evidence has suggested that Pneumocystis carinii exists as separate mating types, and expresses and regulates proteins that govern meiosis and progression of the life cycle. This study was undertaken to investigate the activity of three life cycle-regulatory proteins in Pneumocystis, including two proteins essential in mating signaling, and a putative meiotic regulator, to determine the conditions under which they are most active. This study used V5/HIS-tagged PCRan1p, PCSte20p, and PCCbk1, purified from Saccharomyces cerevisiae strain, INVSC, as well as an in vitro Escherichia coli protein expression system to determine the optimal expression conditions of each protein in the presence of varying pH, temperature, and metal ions. These studies demonstrate an atypical enzymatic activity in PCRan1p, whereby the kinase was most active in the environmental conditions between 10 and 25 degrees C, compared with a dramatic reduction in activity above 30 degrees C, temperatures typically found within mammalian hosts. Circular dichroism and fluorescence spectroscopy suggest that PCRan1p becomes partially unfolded at 25 degrees C, leading to its most active conformation, whereas continued unfolding as temperature increases results in strongly suppressed activity. These studies suggest that, in vivo, while under conditions within the mammalian lung (typically 37 degrees C), PCRan1p kinase activity is largely suppressed, allowing better conditions for the activation of meiosis, whereas in ex vivo environments, PCRan1p kinase activity increases to arrest progression of the life cycle until conditions become more favorable.
Insights
Pneumocystis carinii life cycle proteins show temperature-dependent activity. Kinase PCRan1p is most active at cooler temperatures, suggesting suppressed activity in mammalian hosts to allow meiosis.
Area of Science:
- Mycology
- Molecular Biology
- Immunocompromised Host Pathogenesis
Background:
- Pneumocystis is an opportunistic fungal pathogen causing pneumonia in immunocompromised individuals.
- Pneumocystis carinii has distinct mating types and regulates its life cycle via specific proteins.
Purpose of the Study:
- Investigate the activity of three Pneumocystis life cycle-regulatory proteins (PCRan1p, PCSte20p, PCCbk1).
- Determine optimal conditions (pH, temperature, metal ions) for protein activity.
- Understand how temperature affects PCRan1p kinase activity and its role in the P. carinii life cycle.
Main Methods:
- Purification of V5/HIS-tagged proteins (PCRan1p, PCSte20p, PCCbk1) from Saccharomyces cerevisiae.
- In vitro protein expression and activity assays using an Escherichia coli system.
- Analysis of protein activity under varying pH, temperature, and metal ion concentrations.
- Circular dichroism and fluorescence spectroscopy to assess protein conformation and stability.
Main Results:
- PCRan1p kinase exhibits atypical activity, with optimal function between 10-25°C and significantly reduced activity above 30°C.
- Protein unfolding at 25°C leads to the most active conformation; further unfolding at higher temperatures suppresses activity.
- In vivo conditions (37°C) in mammalian lungs suppress PCRan1p activity, favoring meiosis.
Conclusions:
- PCRan1p kinase activity is temperature-sensitive, being suppressed at mammalian host temperatures.
- Suppressed PCRan1p activity in vivo may facilitate meiotic progression in Pneumocystis.
- Ex vivo conditions increase PCRan1p activity, potentially arresting the life cycle until favorable conditions arise.
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