Evidence map›Paper›PMID 17635994›Full record

ArticleJournal of cell science2007

T6BP and NDP52 are myosin VI binding partners with potential roles in cytokine signalling and cell adhesion.

Brooke Morriswood, Grigory Ryzhakov, Claudia Puri, Susan D Arden, Rhys Roberts, Calliope Dendrou, John Kendrick-Jones, Folma Buss

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Journal of cell science, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03430024 (Nuclear Myosin VI - a Therapeutic Target in Estrogen Receptor Positive Breast Cancer?), which is not on this map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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.

NCT03430024 unknown statusnot on this mapstarted 2019, after this paper: background citation

Nuclear Myosin VI - a Therapeutic Target in Estrogen Receptor Positive Breast Cancer?

TypeobservationalSponsorMaidstone & Tunbridge Wells NHS TrustRan2019 to 2020Enrolled120ConditionsBreast CancerArmsAssociation of Myosin VI with oestrogen receptor
3 · Its place in the literature

Who cites it

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 95 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Cardiolipin membranes drive Myosin VI activation, oligomerization, and processive cargo transport.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  6. Mitophagy plays a "double-edged sword" role in the radiosensitivity of cancer cells.Journal of cancer research and clinical oncology · 2024
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  7. The twoFrontiers in physiology · 2024
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  11. Article
  12. Review
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  14. Article
  15. Autophagy receptors as viral targets.Cellular & molecular biology letters · 2021
    Review
  16. Article
  17. Diverse functions of myosin VI in spermiogenesis.Histochemistry and cell biology · 2021
    Review
  18. Article
  19. Article
  20. Article

1 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

8 authors at 3 institutions in 1 country.

Brooke MorriswoodMRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH, UK.
Grigory Ryzhakov
Claudia Puri
Susan D Arden
Rhys Roberts
Calliope Dendrou
John Kendrick-Jones
Folma Buss
MRC Laboratory of Molecular Biology · GBUniversity of Cambridge · GBWellcome Trust · GB

Funding

Medical Research Council MC_U105184323Wellcome Trust 071162
6 · The paper itself

Abstract

Myosin VI has been implicated in many cellular processes including endocytosis, secretion, membrane ruffling and cell motility. We carried out a yeast two-hybrid screen and identified TRAF6-binding protein (T6BP) and nuclear dot protein 52 (NDP52) as myosin VI binding partners. Myosin VI interaction with T6BP and NDP52 was confirmed in vitro and in vivo and the binding sites on each protein were accurately mapped. Immunofluorescence and electron microscopy showed that T6BP, NDP52 and myosin VI are present at the trans side of the Golgi complex, and on vesicles in the perinuclear region. Although the SKICH domain in T6BP and NDP52 does not mediate recruitment into membrane ruffles, loss of T6BP and NDP52 in RNAi knockdown cells results in reduced membrane ruffling activity and increased stress fibre and focal adhesion formation. Furthermore, we observed in these knockdown cells an upregulation of constitutive secretion of alkaline phosphatase, implying that both proteins act as negative regulators of secretory traffic at the Golgi complex. T6BP was also found to inhibit NF-kappaB activation, implicating it in the regulation of TRAF6-mediated cytokine signalling. Thus myosin VI-T6BP interactions may link membrane trafficking pathways with cell adhesion and cytokine-dependent cell signalling.

Indexed as

Cell AdhesionActinsAlkaline PhosphataseBinding SitesCell LineCell MembraneCytokinesCytoskeletonGolgi ApparatusHeLa CellsHumansIntracellular Signaling Peptides and ProteinsMetabolic Networks and PathwaysMicroscopy, Electron, TransmissionMyosin Heavy ChainsNeoplasm ProteinsActinsAlkaline PhosphataseCALCOCO2 protein, humanCytokinesIntracellular Signaling Peptides and ProteinsMyosin Heavy Chainsmyosin VINeoplasm ProteinsNF-kappa BNuclear ProteinsTAX1BP1 protein, humanTNF Receptor-Associated Factor 6

Identifiers

PMID17635994
PMCPMC2621013
OpenAlexW2052729357

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.