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Global Molecular Response of to Zinc Deprivation: Analyses at Transcript, Protein and MicroRNA Levels. | LitMetric

AI Article Synopsis

  • - Zinc is crucial for all organisms and plays a role in the host's defense against pathogens by limiting metal availability, which fungi like Paracoccidioides use for growth.
  • - The study focused on how fungal pathogens adapt at the genetic and protein levels when zinc supply is low, identifying 19 microRNAs linked to zinc homeostasis and three that showed significant changes.
  • - Findings suggest that these microRNAs help regulate important zinc transporters and transcription factors, indicating that fungi undergo metabolic changes to cope with zinc deprivation.

Article Abstract

Zinc is one of the main micronutrients for all organisms. One of the defense mechanisms used by the host includes the sequestration of metals used in fungal metabolism, such as iron and zinc. There are several mechanisms that maintain the balance in the intracellular zinc supply. MicroRNAs are effector molecules of responses between the pathogen and host, favoring or preventing infection in many microorganisms. Fungi of the genus are thermodimorphic and the etiological agents of paracoccidioidomycosis (PCM). In the current pandemic scenario world mycosis studies continue to be highly important since a significant number of patients with COVID-19 developed systemic mycoses, co-infections that complicated their clinical condition. The objective was to identify transcriptomic and proteomic adaptations in during zinc deprivation. Nineteen microRNAs were identified, three of which were differentially regulated. Target genes regulated by those microRNAs are elements of zinc homeostasis such as ZRT1, ZRT3 and COT1 transporters. Transcription factors that have zinc in their structure are also targets of those miRNAs. Transcriptional and proteomic data suggest that undergoes metabolic remodeling to survive zinc deprivation and that miRNAs may be part of the regulatory process.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056003PMC
http://dx.doi.org/10.3390/jof9030281DOI Listing

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