Evidence map›Paper›PMID 23666623›Full record

ArticleEukaryotic cell2013

The spatial distribution of the exocyst and actin cortical patches is sufficient to organize hyphal tip growth.

David Caballero-Lima, Iliyana N Kaneva, Simon P Watton, Peter E Sudbery, C Jeremy Craven

Open access · diamondAbstract read
In one paragraph

Article in Eukaryotic cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
11.6field-weighted citation impact, top 2% 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

27 citing papers in PubMed, 52 citations in OpenAlex.

  1. Emerging Roles of Exocyst Complex in Fungi: A Review.Journal of fungi (Basel, Switzerland) · 2024
    Review
  2. From Jekyll to Hyde: The Yeast-Hyphal Transition ofPathogens (Basel, Switzerland) · 2021
    Review
  3. Review
  4. Article
  5. Overexpression ofSmall GTPases · 2020
    Article
  6. The Role of Secretory Pathways inJournal of fungi (Basel, Switzerland) · 2020
    Review
  7. Exocyst subunitJournal of biosciences · 2020
    Article
  8. Off the wall: The rhyme and reason ofCell surface (Amsterdam, Netherlands) · 2019
    Review
  9. Candida albicansmBio · 2019
    Article
  10. Review
  11. Candida albicans Hyphae: From Growth Initiation to Invasion.Journal of fungi (Basel, Switzerland) · 2018
    Review
  12. Article
  13. Cell Biology of Hyphal Growth.Microbiology spectrum · 2017
    Review
  14. Article
  15. Article
  16. Review
  17. The Exocyst Complex in Health and Disease.Frontiers in cell and developmental biology · 2016
    Review
  18. Article
  19. Article
  20. Phosphatidylinositol-4-phosphate-dependent membrane traffic is critical for fungal filamentous growth.Proceedings of the National Academy of Sciences of the United States of America · 2015
    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

5 authors at 1 institution in 1 country.

David Caballero-LimaDepartment of Molecular Biology and Biotechnology, University of Sheffield, Sheffield, United Kingdom.
Iliyana N Kaneva
Simon P Watton
Peter E Sudbery
C Jeremy Craven
University of Sheffield · GB

Funding

Biotechnology and Biological Sciences Research Council BB/J002305/1Wellcome TrustWellcome Trust GR077544AIA
6 · The paper itself

Abstract

In the hyphal tip of Candida albicans we have made detailed quantitative measurements of (i) exocyst components, (ii) Rho1, the regulatory subunit of (1,3)-β-glucan synthase, (iii) Rom2, the specialized guanine-nucleotide exchange factor (GEF) of Rho1, and (iv) actin cortical patches, the sites of endocytosis. We use the resulting data to construct and test a quantitative 3-dimensional model of fungal hyphal growth based on the proposition that vesicles fuse with the hyphal tip at a rate determined by the local density of exocyst components. Enzymes such as (1,3)-β-glucan synthase thus embedded in the plasma membrane continue to synthesize the cell wall until they are removed by endocytosis. The model successfully predicts the shape and dimensions of the hyphae, provided that endocytosis acts to remove cell wall-synthesizing enzymes at the subapical bands of actin patches. Moreover, a key prediction of the model is that the distribution of the synthase is substantially broader than the area occupied by the exocyst. This prediction is borne out by our quantitative measurements. Thus, although the model highlights detailed issues that require further investigation, in general terms the pattern of tip growth of fungal hyphae can be satisfactorily explained by a simple but quantitative model rooted within the known molecular processes of polarized growth. Moreover, the methodology can be readily adapted to model other forms of polarized growth, such as that which occurs in plant pollen tubes.

Indexed as

ActinsCandida albicansCell WallEndocytosisFungal ProteinsHumansHyphaeModels, BiologicalTransport VesiclesActinsFungal Proteins

Identifiers

PMID23666623
PMCPMC3697460
OpenAlexW2165624477

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.