Evidence map›Paper›PMID 35255079›Full record

ArticlePLoS genetics2022

Transcriptome and proteome profiling reveals complex adaptations of Candida parapsilosis cells assimilating hydroxyaromatic carbon sources.

Andrea Cillingová, Renáta Tóth, Anna Mojáková, Igor Zeman, Romana Vrzoňová, Barbara Siváková, Peter Baráth, Martina Neboháčová, Zuzana Klepcová, Filip Brázdovič and 11 more

Abstract read
In one paragraph

Article in PLoS genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Review
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  4. Small pangenome ofmBio · 2025
    Article
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  8. The role ofJournal of medical microbiology · 2024
    Article
  9. Article
  10. Chromosome-Level Genome Assembly of the Yeast Candida verbasci.Microbiology resource announcements · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Andrea CillingováDepartment of Biochemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.ORCID 0000-0003-2652-3662
Renáta TóthHCEMM-USZ Department of Microbiology, University of Szeged, Szeged, Hungary.
Anna MojákováDepartment of Biochemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.
Igor ZemanDepartment of Biochemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.ORCID 0000-0003-2526-9324
Romana VrzoňováDepartment of Biochemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.
Barbara SivákováInstitute of Chemistry, Slovak Academy of Sciences, Bratislava, Slovakia.
Peter BaráthInstitute of Chemistry, Slovak Academy of Sciences, Bratislava, Slovakia.ORCID 0000-0001-7330-955X
Martina NeboháčováDepartment of Biochemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.ORCID 0000-0003-4486-2713
Zuzana KlepcováDepartment of Biochemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.
Filip BrázdovičDepartment of Biochemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.ORCID 0000-0002-1566-5967
Hana LichancováDepartment of Biochemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.
Viktória HodorováDepartment of Biochemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.
Broňa BrejováDepartment of Computer Science, Faculty of Mathematics, Physics and Informatics, Comenius University in Bratislava, Bratislava, Slovakia.
Tomáš VinařDepartment of Applied Informatics, Faculty of Mathematics, Physics and Informatics, Comenius University in Bratislava, Bratislava, Slovakia.ORCID 0000-0003-3898-3447
Sofia MutalováDepartment of Biochemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.
Veronika VozárikováDepartment of Genetics, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.ORCID 0000-0003-0852-9032
Giacomo MuttiInstitute for Research in Biomedicine (IRB), The Barcelona Institute of Science and Technology, Barcelona, Spain.ORCID 0000-0002-8687-3333
Ľubomír TomáškaDepartment of Genetics, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.ORCID 0000-0003-4886-1910
Atilla GácserHCEMM-USZ Department of Microbiology, University of Szeged, Szeged, Hungary.ORCID 0000-0003-2939-9580
Toni GabaldónInstitute for Research in Biomedicine (IRB), The Barcelona Institute of Science and Technology, Barcelona, Spain.ORCID 0000-0003-0019-1735
Jozef NosekDepartment of Biochemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.ORCID 0000-0002-1020-5451

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many fungal species utilize hydroxyderivatives of benzene and benzoic acid as carbon sources. The yeast Candida parapsilosis metabolizes these compounds via the 3-oxoadipate and gentisate pathways, whose components are encoded by two metabolic gene clusters. In this study, we determine the chromosome level assembly of the C. parapsilosis strain CLIB214 and use it for transcriptomic and proteomic investigation of cells cultivated on hydroxyaromatic substrates. We demonstrate that the genes coding for enzymes and plasma membrane transporters involved in the 3-oxoadipate and gentisate pathways are highly upregulated and their expression is controlled in a substrate-specific manner. However, regulatory proteins involved in this process are not known. Using the knockout mutants, we show that putative transcriptional factors encoded by the genes OTF1 and GTF1 located within these gene clusters function as transcriptional activators of the 3-oxoadipate and gentisate pathway, respectively. We also show that the activation of both pathways is accompanied by upregulation of genes for the enzymes involved in β-oxidation of fatty acids, glyoxylate cycle, amino acid metabolism, and peroxisome biogenesis. Transcriptome and proteome profiles of the cells grown on 4-hydroxybenzoate and 3-hydroxybenzoate, which are metabolized via the 3-oxoadipate and gentisate pathway, respectively, reflect their different connection to central metabolism. Yet we find that the expression profiles differ also in the cells assimilating 4-hydroxybenzoate and hydroquinone, which are both metabolized in the same pathway. This finding is consistent with the phenotype of the Otf1p-lacking mutant, which exhibits impaired growth on hydroxybenzoates, but still utilizes hydroxybenzenes, thus indicating that additional, yet unidentified transcription factor could be involved in the 3-oxoadipate pathway regulation. Moreover, we propose that bicarbonate ions resulting from decarboxylation of hydroxybenzoates also contribute to differences in the cell responses to hydroxybenzoates and hydroxybenzenes. Finally, our phylogenetic analysis highlights evolutionary paths leading to metabolic adaptations of yeast cells assimilating hydroxyaromatic substrates.

Indexed as

Candida parapsilosisGentisatesCarbonHydroxybenzoatesPhylogenyProteomeProteomicsSaccharomyces cerevisiaeTranscriptomeCarbonGentisatesHydroxybenzoatesProteome

Identifiers

PMID35255079
PMCPMC8929692

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.