Evidence map›Paper›PMID 38704808›Full record

ArticleMycopathologia2024

The StuA Transcription Factor and Alternative Splicing Mechanisms Drive the Levels of MAPK Hog1 Transcripts in the Dermatophyte Trichophyton rubrum.

Leonardo Martins-Santana, Monise Fazolin Petrucelli, Pablo R Sanches, Fausto Almeida, Nilce M Martinez-Rossi, Antonio Rossi

Abstract read
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In one paragraph

Article in Mycopathologia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. The Transcription Factor StuA Regulates Oxidative Stress-Responsive Genes inInternational journal of molecular sciences · 2024
    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

6 authors.

Leonardo Martins-SantanaDepartment of Genetics, Ribeirão Preto Medical Schoool, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-5074-023X
Monise Fazolin PetrucelliDepartment of Genetics, Ribeirão Preto Medical Schoool, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-7136-3990
Pablo R SanchesDepartment of Genetics, Ribeirão Preto Medical Schoool, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-8942-8905
Fausto AlmeidaDepartment of Biochemistry and Immunology, Ribeirão Preto Medical Schoool, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-3782-3698
Nilce M Martinez-RossiDepartment of Genetics, Ribeirão Preto Medical Schoool, University of São Paulo, Ribeirão Preto, São Paulo, Brazil. nmmrossi@usp.br.ORCID http://orcid.org/0000-0002-5723-4276
Antonio RossiDepartment of Genetics, Ribeirão Preto Medical Schoool, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.ORCID http://orcid.org/0000-0003-1951-4741

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 307871/2021-5Conselho Nacional de Desenvolvimento Científico e Tecnológico 307876/2021-7Fundação de Amparo à Pesquisa do Estado de São Paulo proc. no. 2019/22596-9
6 · The paper itself

Abstract

Trichophyton rubrum is a human fungal pathogen that causes dermatophytosis, an infection that affects keratinized tissues. Integrated molecular signals coordinate mechanisms that control pathogenicity. Transcriptional regulation is a core regulation of relevant fungal processes. Previous RNA sequencing data revealed that the absence of the transcription factor StuA resulted in the differential expression of the MAPK-related high glycerol osmolarity gene (hog1) in T. rubrum. Here we validated the role of StuA in regulating the transcript levels of hog1. We showed through RT-qPCR that transcriptional regulation controls hog1 levels in response to glucose, keratin, and co-culture with human keratinocytes. In addition, we also detected hog1 pre-mRNA transcripts that underwent alternative splicing, presenting intron retention in a StuA-dependent mechanism. Our findings suggest that StuA and alternative splicing simultaneously, but not dependently, coordinate hog1 transcript levels in T. rubrum. As a means of preventing and treating dermatophytosis, our results contribute to the search for new potential drug therapies based on the molecular aspects of signaling pathways in T. rubrum.

Indexed as

Alternative SplicingArthrodermataceaeGene Expression Regulation, FungalMitogen-Activated Protein KinasesTineaTranscription FactorsGlucoseHumansKeratinocytesKeratinsReal-Time Polymerase Chain ReactionGlucoseKeratinsMitogen-Activated Protein KinasesTranscription FactorsAlternative splicingDermatophyteHog1MAPKStuATrichophyton rubrum

Identifiers

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Read underepoch 390

Registered trials

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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.