Evidence map›Paper›PMID 14747334›Full record

ArticleBiophysical journal2004

Disruption of Caenorhabditis elegans muscle structure and function caused by mutation of troponin I.

A K Burkeen, S L Maday, K K Rybicka, J A Sulcove, J Ward, M M Huang, R Barstead, C Franzini-Armstrong, T StC Allen

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Biophysical journal, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.6field-weighted citation impact, top 46% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Hsf1 is essential for proteotoxic stress response in smyd1b-deficient embryos and fish survival under heat shock.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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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

9 authors at 3 institutions in 1 country.

A K BurkeenBiology Department, Oberlin College, Oberlin, Ohio 44074-1097, USA.
S L Maday
K K Rybicka
J A Sulcove
J Ward
M M Huang
R Barstead
C Franzini-Armstrong
T StC Allen
Oberlin College · USUniversity of Pennsylvania · USOklahoma Medical Research Foundation · US

Funding

VASCULAR SMOOTH MUSCLEP01HL015835 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI GOLDMAN, YALE E · 1985 to 2002
$5.5M
NHLBI NIH HHS 5-PO1-HL15835
6 · The paper itself

Abstract

Caenorhabditis elegans strains mutant for the unc-27 gene show abnormal locomotion and muscle structure. Experiments revealed that unc-27 is one of four C. elegans troponin I genes and that three mutant alleles truncate the protein: recessive and presumed null allele e155 terminates after nine codons; semidominant su142sd eliminates the inhibitory and C-terminal regions; and semidominant su195sd abbreviates the extreme C-terminus. Assays of in vivo muscular performance at high and low loads indicated that su142sd is most deleterious, with e155 least and su195sd intermediate. Microscopy revealed in mutant muscle a prevalent disorder of dense body positioning and a less well defined sarcomeric structure, with small islands of thin filaments interspersed within the overlap region of A bands and even within the H zone. The mutants' rigid paralysis and sarcomeric disarray are consistent with unregulated contraction of the sarcomeres, in which small portions of each myofibril shorten irregularly and independently of one another, thereby distorting the disposition of filaments. The exacerbated deficits of su142sd worms are compatible with involvement in vivo of the N-terminal portion of troponin I in enhancing force production, and the severe impairment associated with su195sd highlights importance of the extreme C-terminus in the protein's inhibitory function.

Indexed as

SwimmingAgingAmino Acid SequenceAnimalsCaenorhabditis elegansMolecular Sequence DataMovement DisordersMuscle, SkeletalMutagenesis, Site-DirectedMutationRecombinant ProteinsSarcomeresSequence Homology, Amino AcidStructure-Activity RelationshipTask Performance and AnalysisTissue DistributionRecombinant ProteinsTroponin I

Identifiers

PMID14747334
PMCPMC1303946
OpenAlexW1994797049

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.