Evidence map›Paper›PMID 25485759›Full record

ArticleNature neuroscience2015

PlexinA1 is a new Slit receptor and mediates axon guidance function of Slit C-terminal fragments.

Céline Delloye-Bourgeois, Arnaud Jacquier, Camille Charoy, Florie Reynaud, Homaira Nawabi, Karine Thoinet, Karine Kindbeiter, Yutaka Yoshida, Yvrick Zagar, Youxin Kong and 4 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Nature neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

68 citing papers in PubMed, 109 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Structure and evolution of neuronal wiring receptors and ligands.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Review
  20. Review

8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 3 countries.

Céline Delloye-BourgeoisUniversity of Lyon, University Claude Bernard Lyon 1, CGphiMC UMR CNRS 5534, Lyon, France.
Arnaud JacquierUniversity of Lyon, University Claude Bernard Lyon 1, CGphiMC UMR CNRS 5534, Lyon, France.
Camille CharoyUniversity of Lyon, University Claude Bernard Lyon 1, CGphiMC UMR CNRS 5534, Lyon, France.
Florie ReynaudUniversity of Lyon, University Claude Bernard Lyon 1, CGphiMC UMR CNRS 5534, Lyon, France.
Homaira NawabiUniversity of Lyon, University Claude Bernard Lyon 1, CGphiMC UMR CNRS 5534, Lyon, France.
Karine ThoinetUniversity of Lyon, University Claude Bernard Lyon 1, CGphiMC UMR CNRS 5534, Lyon, France.
Karine KindbeiterUniversity of Lyon, University Claude Bernard Lyon 1, CGphiMC UMR CNRS 5534, Lyon, France.
Yutaka YoshidaDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Yvrick Zagar1] INSERM, UMRS_U968, Institut de la Vision, Paris, France. [2] Sorbonne Universités, Université Pierre et Marie Curie (UPMC) University of Paris 06, Institut de la Vision, Paris, France. [3] CNRS, UMR_7210, Paris, France.
Youxin KongWellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
Yvonne E JonesWellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
Julien FalkUniversity of Lyon, University Claude Bernard Lyon 1, CGphiMC UMR CNRS 5534, Lyon, France.
Alain Chédotal1] INSERM, UMRS_U968, Institut de la Vision, Paris, France. [2] Sorbonne Universités, Université Pierre et Marie Curie (UPMC) University of Paris 06, Institut de la Vision, Paris, France. [3] CNRS, UMR_7210, Paris, France.ORCID 0000000175773794
Valérie CastellaniUniversity of Lyon, University Claude Bernard Lyon 1, CGphiMC UMR CNRS 5534, Lyon, France.
Université Claude Bernard Lyon 1 · FRCentre for Human Genetics · GBCentre National de la Recherche Scientifique · FRCincinnati Children's Hospital Medical Center · US

Funding

Cancer Research UK 10976Cancer Research UK 17721Medical Research Council MR/M000141/1
6 · The paper itself

Abstract

Robo-Slit and Plexin-Semaphorin signaling participate in various developmental and pathogenic processes. During commissural axon guidance in the spinal cord, chemorepulsion by Semaphorin3B and Slits controls midline crossing. Slit processing generates an N-terminal fragment (SlitN) that binds to Robo1 and Robo2 receptors and mediates Slit repulsive activity, as well as a C-terminal fragment (SlitC) with an unknown receptor and bioactivity. We identified PlexinA1 as a Slit receptor and found that it binds the C-terminal Slit fragment specifically and transduces a SlitC signal independently of the Robos and the Neuropilins. PlexinA1-SlitC complexes are detected in spinal cord extracts, and ex vivo, SlitC binding to PlexinA1 elicits a repulsive commissural response. Analysis of various ligand and receptor knockout mice shows that PlexinA1-Slit and Robo-Slit signaling have complementary roles during commissural axon guidance. Thus, PlexinA1 mediates both Semaphorin and Slit signaling, and Slit processing generates two active fragments, each exerting distinct effects through specific receptors.

Indexed as

AnimalsAxonsCells, CulturedChick EmbryoGenotypeGrowth ConesMiceNerve Tissue ProteinsPeptide FragmentsReceptors, Cell SurfaceRNA, Small InterferingSpinal CordNerve Tissue ProteinsPeptide FragmentsPlxna1 protein, mouseReceptors, Cell SurfaceRNA, Small Interfering

Identifiers

PMID25485759
OpenAlexW2080738927

What OpenQuestion holds

Textmetadata
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.