Evidence map›Paper›PMID 28814742›Full record

ArticleScientific reports2017

The Candida albicans HIR histone chaperone regulates the yeast-to-hyphae transition by controlling the sensitivity to morphogenesis signals.

Sabrina Jenull, Michael Tscherner, Megha Gulati, Clarissa J Nobile, Neeraj Chauhan, Karl Kuchler

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 21% of its field
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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Proteome Remodelling inJournal of fungi (Basel, Switzerland) · 2026
    Article
  3. Article
  4. Antifungal and antibiofilm effects of probioticFrontiers in cellular and infection microbiology · 2024
    Article
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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 at 5 institutions in 2 countries.

Sabrina JenullMedical University of Vienna, Max F. Perutz Laboratories, Department of Medical Biochemistry, Campus Vienna Biocenter, Dr.-Bohr-Gasse 9/2, A-1030, Vienna, Austria.
Michael TschernerMedical University of Vienna, Max F. Perutz Laboratories, Department of Medical Biochemistry, Campus Vienna Biocenter, Dr.-Bohr-Gasse 9/2, A-1030, Vienna, Austria.
Megha GulatiDepartment of Molecular and Cell Biology, School of Natural Sciences, University of California-Merced, Merced, CA, USA.
Clarissa J NobileDepartment of Molecular and Cell Biology, School of Natural Sciences, University of California-Merced, Merced, CA, USA.
Neeraj ChauhanPublic Health Research Institute, Department of Microbiology, Biochemistry and Molecular Genetics, New Jersey Medical School - Rutgers, The State University of New Jersey, Newark, New Jersey, USA.
Karl KuchlerMedical University of Vienna, Max F. Perutz Laboratories, Department of Medical Biochemistry, Campus Vienna Biocenter, Dr.-Bohr-Gasse 9/2, A-1030, Vienna, Austria. karl.kuchler@meduniwien.ac.at.
University of California, Merced · USCenter for Systems Biology · USMax Perutz Labs · ATRutgers, The State University of New Jersey · USVienna Biocenter · AT

Funding

The Candida albicans acetylome in fungal virulenceR01AI124499 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI CHAUHAN, NEERAJ · 2016 to 2019
$1.6M
Genetic Analysis of the Transcriptional Network Governing C. albicans BiofilmsR00AI100896 · NIAID · UNIVERSITY OF CALIFORNIA, MERCED · PI NOBILE, CLARISSA JANE · 2014 to 2015
$498k
NIAID NIH HHS R00 AI100896NIAID NIH HHS R01 AI124499
6 · The paper itself

Abstract

Morphological plasticity such as the yeast-to-hyphae transition is a key virulence factor of the human fungal pathogen Candida albicans. Hyphal formation is controlled by a multilayer regulatory network composed of environmental sensing, signaling, transcriptional modulators as well as chromatin modifications. Here, we demonstrate a novel role for the replication-independent HIR histone chaperone complex in fungal morphogenesis. HIR operates as a crucial modulator of hyphal development, since genetic ablation of the HIR complex subunit Hir1 decreases sensitivity to morphogenetic stimuli. Strikingly, HIR1-deficient cells display altered transcriptional amplitudes upon hyphal initiation, suggesting that Hir1 affects transcription by establishing transcriptional thresholds required for driving morphogenetic cell-fate decisions. Furthermore, ectopic expression of the transcription factor Ume6, which facilitates hyphal maintenance, rescues filamentation defects of hir1Δ/Δ cells, suggesting that Hir1 impacts the early phase of hyphal initiation. Hence, chromatin chaperone-mediated fine-tuning of transcription is crucial for driving morphogenetic conversions in the fungal pathogen C. albicans.

Indexed as

Signal TransductionCandida albicansEctopic Gene ExpressionFungal ProteinsGene DeletionHistone ChaperonesHyphaeModels, BiologicalPhenotypeTranscription FactorsFungal ProteinsHistone ChaperonesTranscription Factors

Identifiers

PMID28814742
PMCPMC5559454
OpenAlexW2744309050

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.