Evidence map›Paper›PMID 16000376›Full record

ArticleMolecular biology of the cell2005

Specific interaction of the actin-binding domain of dystrophin with intermediate filaments containing keratin 19.

Michele R Stone, Andrea O'Neill, Dawn Catino, Robert J Bloch

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

44 citing papers in PubMed, 84 citations in OpenAlex.

  1. Viltolarsen in Japanese Duchenne muscular dystrophy patients: A phase 1/2 study.Annals of clinical and translational neurology · 2020
    Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Adaptability to eccentric exercise training is diminished with age in female mice.Journal of applied physiology (Bethesda, Md. : 1985) · 2023
    Article
  7. Article
  8. Review
  9. Genetic insight into sick sinus syndrome.European heart journal · 2021
    Article
  10. Duchenne muscular dystrophy.Nature reviews. Disease primers · 2021
    Review
  11. Review
  12. Frontiers in genetics · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Epithelial Keratins Modulate cMet Expression and Signaling and Promote InlB-MediatedFrontiers in cellular and infection microbiology · 2018
    Article
  19. Overview of the Muscle Cytoskeleton.Comprehensive Physiology · 2017
    Review
  20. Article
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

4 authors at 1 institution in 1 country.

Michele R StoneDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Andrea O'Neill
Dawn Catino
Robert J Bloch
University of Maryland, Baltimore · US

Funding

Training Program in Cellular &Integrative NeuroscienceT32NS007375 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI KELLER, ASAF · 1994 to 2013
$4.2M
Training Grant in Cardiac and Vascular Cell BiologyT32HL072751 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI FISHER, STEVEN A. · 2003 to 2013
$3.1M
MACROMOLECULES INVOLVED IN SYNAPSE FORMATIONR01NS017282 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI BLOCH, ROBERT J · 1985 to 2004
$1.5M
The Sarcolemma in FSHD and in the myd MouseR21NS043976 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI BLOCH, ROBERT J · 2001 to 2003
$557k
NHLBI NIH HHS T32 HL 072751NHLBI NIH HHS T32 HL072751NINDS NIH HHS NS 17282NINDS NIH HHS NS43976NINDS NIH HHS R01 NS017282NINDS NIH HHS R21 NS043976NINDS NIH HHS T32 NS007375NINDS NIH HHS T32 NS 07375
6 · The paper itself

Abstract

Cytokeratins 8 and 19 concentrate at costameres of striated muscle and copurify with the dystrophin-glycoprotein complex, perhaps through the interaction of the cytokeratins with the actin-binding domain of dystrophin. We overexpressed dystrophin's actin-binding domain (Dys-ABD), K8 and K19, as well as closely related proteins, in COS-7 cells to assess the basis and specificity of their interaction. Dys-ABD alone associated with actin microfilaments. Expressed with K8 and K19, which form filaments, Dys-ABD associated preferentially with the cytokeratins. This interaction was specific, as the homologous ABD of betaI-spectrin failed to interact with K8/K19 filaments, and Dys-ABD did not associate with desmin or K8/K18 filaments. Studies in COS-7 cells and in vitro showed that Dys-ABD binds directly and specifically to K19. Expressed in muscle fibers in vivo, K19 accumulated in the myoplasm in structures that contained dystrophin and spectrin and disrupted the organization of the sarcolemma. K8 incorporated into sarcomeres, with no effect on the sarcolemma. Our results show that dystrophin interacts through its ABD with K19 specifically and are consistent with the idea that cytokeratins associate with dystrophin at the sarcolemma of striated muscle.

Indexed as

ActinsAmino Acid SequenceAnimalsBinding SitesBiomarkersChlorocebus aethiopsCOS CellsDystrophinFluorescent Antibody TechniqueHumansIntermediate FilamentsKeratinsMicrofilament ProteinsMolecular Sequence DataMuscle Fibers, SkeletalProtein Structure, TertiaryActinsBiomarkersDystrophinKeratinsMicrofilament Proteins

Identifiers

PMID16000376
PMCPMC1196337
OpenAlexW2156427063

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.