Evidence map›Paper›PMID 27009204›Full record

ArticleMolecular biology of the cell2016

Eisosomes promote the ability of Sur7 to regulate plasma membrane organization in Candida albicans.

Hong X Wang, Lois M Douglas, Petra Veselá, Reinhard Rachel, Jan Malinsky, James B Konopka

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

22 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  5. Article
  6. Sur7 mediates a novel pathway for PIMolecular biology of the cell · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. SUR7 deletion inJournal of extracellular biology · 2023
    Article
  11. Complementation of an Eisosomal YeastJournal of fungi (Basel, Switzerland) · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Plasma Membrane MCC/Eisosome Domains Promote Stress Resistance in Fungi.Microbiology and molecular biology reviews : MMBR · 2020
    Review
  17. Article
  18. Article
  19. Review
  20. 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 at 3 institutions in 3 countries.

Hong X WangDepartment of Molecular Genetics and Microbiology, Stony Brook University, Stony Brook, NY 11794-5222.
Lois M DouglasDepartment of Molecular Genetics and Microbiology, Stony Brook University, Stony Brook, NY 11794-5222.
Petra VeseláInstitute of Experimental Medicine, Academy of Sciences of the Czech Republic, 142 20 Prague, Czech Republic.
Reinhard RachelCentre for Electron Microscopy, Faculty of Biology and Preclinical Medicine, University of Regensburg, 93053 Regensburg, Germany.
Jan MalinskyInstitute of Experimental Medicine, Academy of Sciences of the Czech Republic, 142 20 Prague, Czech Republic.
James B KonopkaDepartment of Molecular Genetics and Microbiology, Stony Brook University, Stony Brook, NY 11794-5222 james.konopka@stonybrook.edu.
Stony Brook University · USCzech Academy of Sciences, Institute of Experimental Medicine · CZUniversity of Regensburg · DE

Funding

Regulation of Morphogenesis in C. albicansR01AI047837 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI James B Konopka · 2001 to 2026
$8.8M
Regulation of morphogenesis in C. albicansR56AI047837 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI KONOPKA, JAMES B · 2016 to 2016
$440k
NIAID NIH HHS R01 AI047837NIAID NIH HHS R56 AI047837
6 · The paper itself

Abstract

The plasma membrane of the fungal pathogen Candida albicans forms a protective barrier that also mediates many processes needed for virulence, including cell wall synthesis, invasive hyphal morphogenesis, and nutrient uptake. Because compartmentalization of the plasma membrane is believed to coordinate these diverse activities, we examined plasma membrane microdomains termed eisosomes or membrane compartment of Can1 (MCC), which correspond to ∼200-nm-long furrows in the plasma membrane. A pil1∆ lsp1∆ mutant failed to form eisosomes and displayed strong defects in plasma membrane organization and morphogenesis, including extensive cell wall invaginations. Mutation of eisosome proteins Slm2, Pkh2, and Pkh3 did not cause similar cell wall defects, although pkh2∆ cells formed chains of furrows and pkh3∆ cells formed wider furrows, identifying novel roles for the Pkh protein kinases in regulating furrows. In contrast, the sur7∆ mutant formed cell wall invaginations similar to those for the pil1∆ lsp1∆ mutant even though it could form eisosomes and furrows. A PH-domain probe revealed that the regulatory lipid phosphatidylinositol 4,5-bisphosphate was enriched at sites of cell wall invaginations in both the sur7∆ and pil1∆ lsp1∆ cells, indicating that this contributes to the defects. The sur7∆ and pil1∆ lsp1∆ mutants displayed differential susceptibility to various types of stress, indicating that they affect overlapping but distinct functions. In support of this, many mutant phenotypes of the pil1∆ lsp1∆ cells were rescued by overexpressing SUR7 These results demonstrate that C. albicans eisosomes promote the ability of Sur7 to regulate plasma membrane organization.

Indexed as

Candida albicansCell MembraneCell WallEndocytosisFungal ProteinsHyphaeMembrane MicrodomainsMembrane ProteinsPhosphoproteinsProtein KinasesFungal ProteinsMembrane ProteinsPhosphoproteinsProtein Kinases

Identifiers

PMID27009204
PMCPMC4865322
OpenAlexW2332781297

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.