Evidence map›Paper›PMID 32185489›Full record

ReviewCurrent genetics2020

Machinery for fungal heme acquisition.

Simon Labbé, Thierry Mourer, Ariane Brault, Tobias Vahsen

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Heme sensing and trafficking in fungi.Fungal biology reviews · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. 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

4 authors at 1 institution in 1 country.

Simon LabbéDépartement de Biochimie et de Génomique Fonctionnelle, Faculté de Médecine et des Sciences de la santé, Pavillon Z-8, Université de Sherbrooke, 3201, Jean Mignault, Sherbrooke, QC, J1E 4K8, Canada. Simon.Labbe@USherbrooke.ca.ORCID http://orcid.org/0000-0002-4947-523X
Thierry MourerDépartement de Biochimie et de Génomique Fonctionnelle, Faculté de Médecine et des Sciences de la santé, Pavillon Z-8, Université de Sherbrooke, 3201, Jean Mignault, Sherbrooke, QC, J1E 4K8, Canada.
Ariane BraultDépartement de Biochimie et de Génomique Fonctionnelle, Faculté de Médecine et des Sciences de la santé, Pavillon Z-8, Université de Sherbrooke, 3201, Jean Mignault, Sherbrooke, QC, J1E 4K8, Canada.
Tobias VahsenDépartement de Biochimie et de Génomique Fonctionnelle, Faculté de Médecine et des Sciences de la santé, Pavillon Z-8, Université de Sherbrooke, 3201, Jean Mignault, Sherbrooke, QC, J1E 4K8, Canada.
Université de Sherbrooke · CA

Funding

Natural Sciences and Engineering Research Council of Canada RGPIN-2015-2020-04878
6 · The paper itself

Abstract

Iron is essential for nearly all aerobic organisms. One source of iron in nature is in the form of heme. Due to its critical physiological importance as a cofactor for several enzymes, organisms have evolved various means to secure heme for their needs. In the case of heme prototrophs, these organisms possess a highly conserved eight-step biosynthetic pathway. Another means used by many organisms is to acquire heme from external sources. As opposed to the knowledge of enzymes responsible for heme biosynthesis, the nature of the players and mechanisms involved in the acquisition of exogenous heme is limited. This review focuses on a description of newly discovered proteins that have novel functions in heme assimilation in the model organism Schizosaccharomyces pombe. This tractable model allows the use of the power of genetics to selectively block heme biosynthesis, setting conditions to investigate the mechanisms by which external heme is taken up by the cells. Studies have revealed that S. pombe possesses two independent heme uptake systems that require Shu1 and Str3, respectively. Heme-bound iron is captured by Shu1 at the cell surface, triggering its internalization to the vacuole with the aid of ubiquitinated proteins and the ESCRT machinery. In the case of the plasma membrane transporter Str3, it promotes cellular heme import in cells lacking Shu1. The discovery of these two pathways may contribute to gain novel insights into the mechanisms whereby fungi assimilate heme, which is an essentially biological process for their ability to invade and colonize new niches.

Indexed as

AnimalsEndosomal Sorting Complexes Required for TransportFungiHemeMembrane ProteinsSchizosaccharomycesSchizosaccharomyces pombe ProteinsEndosomal Sorting Complexes Required for TransportHemeMembrane ProteinsSchizosaccharomyces pombe ProteinsShu1 protein, S pombeFission yeastGPI-linked heme-binding proteinHemeHemoproteinsMFS-type heme transporter

Identifiers

PMID32185489
OpenAlexW3011204140

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.