Evidence map›Paper›PMID 19766621›Full record

ArticleDevelopmental biology2009

Complex interactions amongst N-cadherin, DLAR, and Liprin-alpha regulate Drosophila photoreceptor axon targeting.

Saurabh Prakash, Helen M McLendon, Catherine I Dubreuil, Aurnab Ghose, Jennifer Hwa, Kelly A Dennehy, Katharine M H Tomalty, Kelsey L Clark, David Van Vactor, Thomas R Clandinin

Abstract read
In one paragraph

Article in Developmental biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-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

25 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Molecular definition of distinct active zone protein machineries for CabioRxiv : the preprint server for biology · 2023
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  6. Assembly of the presynaptic active zone.Current opinion in neurobiology · 2020
    Review
  7. Lar maintains the homeostasis of the hematopoietic organ inDevelopment (Cambridge, England) · 2019
    Article
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  14. Review
  15. Visual circuit assembly requires fine tuning of the novel Ig transmembrane protein Borderless.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  16. Article
  17. Article
  18. Article
  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

10 authors at 2 institutions in 1 country.

Saurabh PrakashDepartment of Neurobiology, 299 W. Campus Drive, Stanford University, Stanford, CA 94305, USA.
Helen M McLendon
Catherine I Dubreuil
Aurnab Ghose
Jennifer Hwa
Kelly A Dennehy
Katharine M H Tomalty
Kelsey L Clark
David Van Vactor
Thomas R Clandinin
Stanford University · USHarvard University · US

Funding

How do photoreceptor axons choose appropriate post-synaptic partners?R01EY015231 · NEI · STANFORD UNIVERSITY · PI CLANDININ, THOMAS ROBERT · 2004 to 2010
$2.5M
NEI NIH HHS R01 EY015231Wellcome Trust
6 · The paper itself

Abstract

The formation of stable adhesive contacts between pre- and post-synaptic neurons represents the initial step in synapse assembly. The cell adhesion molecule N-cadherin, the receptor tyrosine phosphatase DLAR, and the scaffolding molecule Liprin-alpha play critical, evolutionarily conserved roles in this process. However, how these proteins signal to the growth cone and are themselves regulated remains poorly understood. Using Drosophila photoreceptors (R cells) as a model, we evaluate genetic and physical interactions among these three proteins. We demonstrate that DLAR function in this context is independent of phosphatase activity but requires interactions mediated by its intracellular domain. Genetic studies reveal both positive and, surprisingly, inhibitory interactions amongst all three genes. These observations are corroborated by biochemical studies demonstrating that DLAR physically associates via its phosphatase domain with N-cadherin in Drosophila embryos. Together, these data demonstrate that N-cadherin, DLAR, and Liprin-alpha function in a complex to regulate adhesive interactions between pre- and post-synaptic cells and provide a novel mechanism for controlling the activity of Liprin-alpha in the developing growth cone.

Indexed as

AnimalsAxonsCadherinsDrosophila melanogasterDrosophila ProteinsEmbryo, NonmammalianGreen Fluorescent ProteinsImmunoprecipitationIntracellular Signaling Peptides and ProteinsPhosphoproteinsPhotoreceptor Cells, InvertebrateProtein BindingReceptor-Like Protein Tyrosine PhosphatasesSynapsesCadherinsDrosophila ProteinsGreen Fluorescent ProteinsIntracellular Signaling Peptides and ProteinsLar protein, DrosophilaLiprin-alpha protein, DrosophilaPhosphoproteinsReceptor-Like Protein Tyrosine Phosphatases

Identifiers

PMID19766621
PMCPMC2783772
OpenAlexW2017397242

What OpenQuestion holds

Textmetadata
LicenceTDM
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.