Evidence map›Paper›PMID 20510926›Full record

ArticleCell2010

Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearing.

Shin-ichiro Kitajiri, Takeshi Sakamoto, Inna A Belyantseva, Richard J Goodyear, Ruben Stepanyan, Ikuko Fujiwara, Jonathan E Bird, Saima Riazuddin, Sheikh Riazuddin, Zubair M Ahmed and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 122 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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

122 citing papers in PubMed, 1 synthesis or guideline pooled it, 200 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Presbycusis: Pathology, Signal Pathways, and Therapeutic Strategy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  9. Sound-evoked tonic motility of cochlear outer hair cells in mice with stereociliary defects.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. The mechanism of CaThe Journal of biological chemistry · 2025
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 6 institutions in 3 countries.

Shin-ichiro KitajiriLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD 20850, USA.
Takeshi Sakamoto
Inna A Belyantseva
Richard J Goodyear
Ruben Stepanyan
Ikuko Fujiwara
Jonathan E Bird
Saima Riazuddin
Sheikh Riazuddin
Zubair M Ahmed
Jenny E Hinshaw
James Sellers
James R Bartles
John A Hammer
Guy P Richardson
Andrew J Griffith
Gregory I Frolenkov
Thomas B Friedman
National Institutes of Health · USNational Heart Lung and Blood Institute · USUniversity of Kentucky · USUniversity of Sussex · GBCentre of Excellence in Molecular Biology · PKNational Institute on Deafness and Other Communication Disorders · US

Funding

Identification of Genes Causing Syndromic And Nonsyndromic Hearing ImpairmentZIADC000039 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI FRIEDMAN, THOMAS · 2009 to 2025
$48.7M
Myosin XVA and Other Genes Essential for Stereocilia MorphogenesisZIADC000048 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI FRIEDMAN, THOMAS · 2009 to 2025
$23.6M
Molecular Analysis Of Human Hereditary DeafnessZIADC000060 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI ROUX, ISABELLE · 2009 to 2022
$18.4M
Expression Studies of Other Unconventional MyosinsZIAHL004232 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI SELLERS, JAMES · 2009 to 2025
$11.7M
THE ROLES OF ESPINS IN HAIR CELL STEREOCILIAR01DC004314 · NIDCD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BARTLES, JAMES R · 2000 to 2019
$8.0M
Role of CARMIL proteins in cell structure and functionZIAHL006120 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI HAMMER, JOHN A · 2011 to 2022
$7.7M
Myosin XVA and Other Genes Essential for Stereocilia MorphogenesisZ01DC000048 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI FRIEDMAN, THOMAS BAER · 1998 to 2008
$1.7M
Role of Staircase Hair Bundle Morphology in Auditory MechanotransductionR01DC008861 · NIDCD · UNIVERSITY OF KENTUCKY · PI FROLENKOV, GREGORY I · 2009 to 2012
$1.5M
Regulation of outer hair cell electromotility and noise-induced hearing lossR01DC009434 · NIDCD · UNIVERSITY OF KENTUCKY · PI FROLENKOV, GREGORY I · 2009 to 2013
$1.3M
EXPRESSION STUDIES OF OTHER UNCONVENTIONAL MYOSINSZ01HL004232 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI SELLERS, JAMES R. · 2000 to 2008
$1.2M
Clinical Analysis Of Disorders Of Hearing And BalanceZ01DC000064 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI GRIFFITH, ANDREW J · 2001 to 2008
$1.2M
MOLECULAR GENETICS OF USHER SYNDROME TYPE IR00DC009287 · NIDCD · CINCINNATI CHILDRENS HOSP MED CTR · PI AHMED, ZUBAIR M. · 2009 to 2011
$732k
Intramural NIH HHS Z01 DC000048Intramural NIH HHS Z01 DC000064Intramural NIH HHS Z01 DK060100Intramural NIH HHS Z01 HL004232Intramural NIH HHS ZIA DC000039Intramural NIH HHS ZIA DC000048NIDCD NIH HHS R00 DC009287NIDCD NIH HHS R01 DC004314NIDCD NIH HHS R01 DC008861NIDCD NIH HHS R01DC008861NIDCD NIH HHS R01 DC009434NIDCD NIH HHS R01DC009434Wellcome TrustWellcome Trust 071394/Z/03/Z
6 · The paper itself

Abstract

Inner ear hair cells detect sound through deflection of mechanosensory stereocilia. Each stereocilium is supported by a paracrystalline array of parallel actin filaments that are packed more densely at the base, forming a rootlet extending into the cell body. The function of rootlets and the molecules responsible for their formation are unknown. We found that TRIOBP, a cytoskeleton-associated protein mutated in human hereditary deafness DFNB28, is localized to rootlets. In vitro, purified TRIOBP isoform 4 protein organizes actin filaments into uniquely dense bundles reminiscent of rootlets but distinct from bundles formed by espin, an actin crosslinker in stereocilia. We generated mutant Triobp mice (Triobp(Deltaex8/Deltaex8)) that are profoundly deaf. Stereocilia of Triobp(Deltaex8/Deltaex8) mice develop normally but fail to form rootlets and are easier to deflect and damage. Thus, F-actin bundling by TRIOBP provides durability and rigidity for normal mechanosensitivity of stereocilia and may contribute to resilient cytoskeletal structures elsewhere.

Indexed as

Actin CytoskeletonAnimalsDeafnessHair Cells, Auditory, InnerHumansMechanotransduction, CellularMiceMice, KnockoutMicrofilament ProteinsMolecular Sequence DataMicrofilament ProteinsTRIOBP protein, mouse

Identifiers

PMID20510926
PMCPMC2879707
OpenAlexW2084929485

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.