Evidence map›Paper›PMID 20861315›Full record

ArticleMolecular biology of the cell2010

Antagonistic functions of two stardust isoforms in Drosophila photoreceptor cells.

Natalia A Bulgakova, Michaela Rentsch, Elisabeth Knust

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. A Quantitative Model of Sporadic Axonal Degeneration in theThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  4. Article
  5. Article
  6. Frontiers in neuroscience · 2017
    Article
  7. Domain-specific functions of Stardust inRoyal Society open science · 2016
    Article
  8. Article
  9. 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

3 authors.

Natalia A BulgakovaMax-Planck-Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.
Michaela Rentsch
Elisabeth Knust

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Membrane-associated guanylate kinases (MAGUKs) are scaffolding proteins that organize supramolecular protein complexes, thereby partitioning the plasma membrane into spatially and functionally distinct subdomains. Their modular organization is ideally suited to organize protein complexes with cell type- or stage-specific composition, or both. Often more than one MAGUK isoform is expressed by one gene in the same cell, yet very little is known about their individual in vivo functions. Here, we show that two isoforms of Drosophila stardust, Sdt-H (formerly called Sdt-B2) and Sdt-D, which differ in their N terminus, are expressed in adult photoreceptors. Both isoforms associate with Crumbs and PATJ, constituents of the conserved Crumbs-Stardust complex. However, they form distinct complexes, localized at the stalk, a restricted region of the apical plasma membrane. Strikingly, Sdt-H and Sdt-D have antagonistic functions. While Sdt-H overexpression increases stalk membrane length and prevents light-dependent retinal degeneration, Sdt-D overexpression reduces stalk length and enhances light-dependent retinal degeneration. These results suggest that a fine-tuned balance of different Crumbs complexes regulates photoreceptor homeostasis.

Indexed as

AnimalsAnimals, Genetically ModifiedBlotting, WesternDown-RegulationDrosophila melanogasterDrosophila ProteinsEyeEye ProteinsGene Expression Regulation, DevelopmentalGuanylate KinasesImmunoprecipitationMembrane ProteinsMembrane Transport ProteinsMicroscopy, Electron, TransmissionMutationPhotoreceptor Cells, Invertebratecrb protein, DrosophilaDrosophila ProteinsEye ProteinsGuanylate KinasesMembrane ProteinsMembrane Transport ProteinsPar-6 protein, DrosophilaPATJ protein, DrosophilaProtein IsoformsProtein Kinase Csdt protein, Drosophila

Identifiers

PMID20861315
PMCPMC2982133

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Registered trials

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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.