Evidence map›Paper›PMID 24607370›Full record

ArticleDevelopmental biology2014

Exocyst-mediated membrane trafficking is required for branch outgrowth in Drosophila tracheal terminal cells.

Tiffani A Jones, Linda S Nikolova, Ani Schjelderup, Mark M Metzstein

Abstract read
In one paragraph

Article in Developmental biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

  1. TheProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  2. Article
  3. International journal of molecular sciences · 2021
    Review
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  15. Time to make the doughnuts: Building and shaping seamless tubes.Seminars in cell & developmental biology · 2017
    Review
  16. Article
  17. Review
  18. The Exocyst Complex in Health and Disease.Frontiers in cell and developmental biology · 2016
    Review
  19. Article
  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

4 authors at 1 institution in 1 country.

Tiffani A JonesDepartment of Human Genetics, University of Utah, Salt Lake City, UT 84112, USA.
Linda S NikolovaDepartment of Human Genetics, University of Utah, Salt Lake City, UT 84112, USA.
Ani SchjelderupDepartment of Human Genetics, University of Utah, Salt Lake City, UT 84112, USA.
Mark M MetzsteinDepartment of Human Genetics, University of Utah, Salt Lake City, UT 84112, USA. Electronic address: markm@genetics.utah.edu.
University of Utah · US

Funding

TRAINING PROGRAM IN GENETICST32GM007464 · NIGMS · UNIVERSITY OF UTAH · PI GRUNWALD, DAVID J., STANFIELD, GILLIAN · 1985 to 2020
$6.1M
NIGMS NIH HHS T32 GM007464NIGMS NIH HHS T32-GM007464
6 · The paper itself

Abstract

Branching morphogenesis, the process by which cells or tissues generate tree-like networks that function to increase surface area or in contacting multiple targets, is a common developmental motif in multicellular organisms. We use Drosophila tracheal terminal cells, a component of the insect respiratory system, to investigate branching morphogenesis that occurs at the single cell level. Here, we show that the exocyst, a conserved protein complex that facilitates docking and tethering of vesicles at the plasma membrane, is required for terminal cell branch outgrowth. We find that exocyst-deficient terminal cells have highly truncated branches and show an accumulation of vesicles within their cytoplasm and are also defective in subcellular lumen formation. We also show that vesicle trafficking pathways mediated by the Rab GTPases Rab10 and Rab11 are redundantly required for branch outgrowth. In terminal cells, the PAR-polarity complex is required for branching, and we find that the PAR complex is required for proper membrane localization of the exocyst, thus identifying a molecular link between the branching and outgrowth programs. Together, our results suggest a model where exocyst mediated vesicle trafficking facilitates branch outgrowth, while de novo branching requires cooperation between the PAR and exocyst complexes.

Indexed as

AnimalsAnimals, Genetically ModifiedBiological TransportCell ProliferationCytoplasmic VesiclesDrosophila melanogasterDrosophila ProteinsEndocytosisGene Expression Regulation, DevelopmentalGreen Fluorescent ProteinsMicroscopy, ConfocalMicroscopy, Electron, TransmissionMorphogenesisMultiprotein ComplexesProtein Kinase Crab GTP-Binding ProteinsDrosophila ProteinsGreen Fluorescent ProteinsMultiprotein ComplexesPar-6 protein, DrosophilaProtein Kinase Crab GTP-Binding ProteinsSec15 protein, DrosophilaVesicular Transport ProteinsBranching morphogenesisDrosophilaExocyst complexLumenogenesisPAR complexTerminal cellsTrachea

Identifiers

PMID24607370
PMCPMC4041209
OpenAlexW2001520703

What OpenQuestion holds

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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.