Evidence map›Paper›PMID 23143520›Full record

ArticleNature neuroscience2012

A chemical genetic approach reveals distinct EphB signaling mechanisms during brain development.

Michael J Soskis, Hsin-Yi Henry Ho, Brenda L Bloodgood, Michael A Robichaux, Athar N Malik, Bulent Ataman, Alex A Rubin, Janine Zieg, Chao Zhang, Kevan M Shokat and 3 more

Abstract read
In one paragraph

Article in Nature neuroscience, 2012. 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
–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

27 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Eph Receptors in Cancer.Biomedicines · 2023
    Review
  8. Article
  9. Phospho-regulation of mitotic spindle assembly.Cytoskeleton (Hoboken, N.J.) · 2020
    Review
  10. Article
  11. Article
  12. Review
  13. Protein Tyrosine Phosphatase Receptor Type J (PTPRJ) Regulates Retinal Axonal Projections by Inhibiting Eph and Abl Kinases in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Michael J SoskisDepartment of Neurobiology, Harvard Medical School, Boston, Massachusetts, USA.
Hsin-Yi Henry Ho
Brenda L Bloodgood
Michael A Robichaux
Athar N Malik
Bulent Ataman
Alex A Rubin
Janine Zieg
Chao Zhang
Kevan M Shokat
Nikhil Sharma
Christopher W Cowan
Michael E Greenberg

Funding

Medical Scientist Training ProgramT32GM007753 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WALENSKY, LOREN DAVID · 1985 to 2021
$50.0M
SYNAPTIC MECHANISMS IN HIPPOCAMPAL EPILEPTOGENESISP30HD018655 · NICHD · CHILDREN'S HOSPITAL BOSTON · PI POMEROY, SCOTT LOREN · 1985 to 2015
$26.2M
Training in the Molecular Biology of Neurodegeneration and Alzheimer's DiseaseT32AG000222 · NIA · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI Bruce A YANKNER · 1992 to 2026
$18.5M
Neurotrophic Factor Regulation of Gene ExpressionR01NS045500 · NINDS · HARVARD MEDICAL SCHOOL · PI GREENBERG, MICHAEL ELDON · 2003 to 2018
$8.2M
Basic Science Training Program in Drug Abuse ResearchT32DA007290 · NIDA · YALE UNIVERSITY · PI SELF, DAVID W · 1992 to 2017
$6.7M
Super-Resolution ImagingP30NS072030 · NINDS · HARVARD MEDICAL SCHOOL · PI REGEHR, WADE G · 2011 to 2020
$5.8M
Signaling Mechanisms of Retinal Axon GuidanceR01EY018207 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI COWAN, CHRISTOPHER W · 2007 to 2011
$1.9M
NEI NIH HHS R01 EY018207NEI NIH HHS R01-EY-018207NIA NIH HHS T32 AG000222NICHD NIH HHS P30 HD018655NIDA NIH HHS T32 DA007290NIDA NIH HHS T32 DA07290NIGMS NIH HHS T32 GM007753NINDS NIH HHS P30 NS072030NINDS NIH HHS R01 NS045500NINDS NIH HHS R01-NS-045500
6 · The paper itself

Abstract

EphB receptor tyrosine kinases control multiple steps in nervous system development. However, it remains unclear whether EphBs regulate these different developmental processes directly or indirectly. In addition, given that EphBs signal through multiple mechanisms, it has been challenging to define which signaling functions of EphBs regulate particular developmental events. To address these issues, we engineered triple knock-in mice in which the kinase activity of three neuronally expressed EphBs can be rapidly, reversibly and specifically blocked. We found that the tyrosine kinase activity of EphBs was required for axon guidance in vivo. In contrast, EphB-mediated synaptogenesis occurred normally when the kinase activity of EphBs was inhibited, suggesting that EphBs mediate synapse development by an EphB tyrosine kinase-independent mechanism. Taken together, our data indicate that EphBs control axon guidance and synaptogenesis by distinct mechanisms and provide a new mouse model for dissecting EphB function in development and disease.

Indexed as

Amino Acid SequenceAnimalsBrainBrain ChemistryCells, CulturedFemaleGene Knock-In TechniquesHEK293 CellsHumansMiceMice, 129 StrainMice, Inbred C57BLMice, TransgenicMolecular Sequence DataOrgan Culture TechniquesPregnancyReceptors, Eph Family

Identifiers

PMID23143520
PMCPMC3509236

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.