Evidence map›Paper›PMID 22764224›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

Spectraplakins promote microtubule-mediated axonal growth by functioning as structural microtubule-associated proteins and EB1-dependent +TIPs (tip interacting proteins).

Juliana Alves-Silva, Natalia Sánchez-Soriano, Robin Beaven, Melanie Klein, Jill Parkin, Thomas H Millard, Hugo J Bellen, Koen J T Venken, Christoph Ballestrem, Richard A Kammerer and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
3.9field-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

66 citing papers in PubMed, 119 citations in OpenAlex.

  1. GSK-3β coordinates axonal microtubule organization through Shot and Tau.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  10. TheMolecular biology of the cell · 2022
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  11. Cross-linkers at growing microtubule ends generate forces that drive actin transport.Proceedings of the National Academy of Sciences of the United States of America · 2022
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6 more citing papers are in PubMed but not listed here.

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

11 authors at 2 institutions in 2 countries.

Juliana Alves-SilvaFaculty of Life Sciences, Wellcome Trust Centre for Cell-Matrix Research, Manchester M13 9PT, United Kingdom.
Natalia Sánchez-Soriano
Robin Beaven
Melanie Klein
Jill Parkin
Thomas H Millard
Hugo J Bellen
Koen J T Venken
Christoph Ballestrem
Richard A Kammerer
Andreas Prokop
Wellcome Centre for Cell-Matrix Research · GBHoward Hughes Medical Institute · US

Funding

Biotechnology and Biological Sciences Research Council 092403/Z/10/ZBiotechnology and Biological Sciences Research Council BB/C515998/1Biotechnology and Biological Sciences Research Council BB/I002448/1Howard Hughes Medical InstituteWellcome Trust 074343/Z/04/BWellcome Trust 077748Wellcome Trust 077748/Z/05/ZWellcome Trust 078593/Z/05/ZWellcome Trust 087820/Z/08/ZWellcome Trust 092403/Z/10/Z
6 · The paper itself

Abstract

The correct outgrowth of axons is essential for the development and regeneration of nervous systems. Axon growth is primarily driven by microtubules. Key regulators of microtubules in this context are the spectraplakins, a family of evolutionarily conserved actin-microtubule linkers. Loss of function of the mouse spectraplakin ACF7 or of its close Drosophila homolog Short stop/Shot similarly cause severe axon shortening and microtubule disorganization. How spectraplakins perform these functions is not known. Here we show that axonal growth-promoting roles of Shot require interaction with EB1 (End binding protein) at polymerizing plus ends of microtubules. We show that binding of Shot to EB1 requires SxIP motifs in Shot's C-terminal tail (Ctail), mutations of these motifs abolish Shot functions in axonal growth, loss of EB1 function phenocopies Shot loss, and genetic interaction studies reveal strong functional links between Shot and EB1 in axonal growth and microtubule organization. In addition, we report that Shot localizes along microtubule shafts and stabilizes them against pharmacologically induced depolymerization. This function is EB1-independent but requires net positive charges within Ctail which essentially contribute to the microtubule shaft association of Shot. Therefore, spectraplakins are true members of two important classes of neuronal microtubule regulating proteins: +TIPs (tip interacting proteins; plus end regulators) and structural MAPs (microtubule-associated proteins). From our data we deduce a model that relates the different features of the spectraplakin C terminus to the two functions of Shot during axonal growth.

Indexed as

ActinsAmino Acid MotifsAnimalsAnimals, Genetically ModifiedAxonsDrosophila melanogasterDrosophila ProteinsFemaleGene Expression Regulation, DevelopmentalGene Knockout TechniquesGrowth ConesMaleMiceMicrofilament ProteinsMicrotubule-Associated ProteinsMutationActinsDrosophila ProteinsEB1 microtubule binding proteinsMacf1 protein, mouseMicrofilament ProteinsMicrotubule-Associated ProteinsNerve Tissue Proteinsshot protein, Drosophila

Identifiers

PMID22764224
PMCPMC3666083
OpenAlexW1970639161

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.