Evidence map›Paper›PMID 21237266›Full record

ArticleMechanisms of development

Cardiac remodeling in Drosophila arises from changes in actin gene expression and from a contribution of lymph gland-like cells to the heart musculature.

Ankita P Shah, Upendra Nongthomba, Kathleen K Kelly Tanaka, Michele L B Denton, Stryder M Meadows, Naomi Bancroft, Marco R Molina, Richard M Cripps

Open access · greenAbstract read
In one paragraph

Article in Mechanisms of development. 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
0.9field-weighted citation impact, top 28% 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, 30 citations in OpenAlex.

  1. Article
  2. Drosophila as a Model to Understand Second Heart Field Development.Journal of cardiovascular development and disease · 2023
    Review
  3. Article
  4. Cells · 2021
    Review
  5. Article
  6. Article
  7. Absence of the Drosophila jump muscle actin Act79B is compensated by up-regulation of Act88F.Developmental dynamics : an official publication of the American Association of Anatomists · 2018
    Article
  8. Article
  9. Review
  10. On the Morphology of the Drosophila Heart.Journal of cardiovascular development and disease · 2016
    Review
  11. Regulatory Networks that Direct the Development of Specialized Cell Types in theJournal of cardiovascular development and disease · 2016
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
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 2 institutions in 2 countries.

Ankita P ShahDepartment of Biology, University of New Mexico, Albuquerque, NM 87131-0001, USA.
Upendra Nongthomba
Kathleen K Kelly Tanaka
Michele L B Denton
Stryder M Meadows
Naomi Bancroft
Marco R Molina
Richard M Cripps
University of New Mexico · USIndian Institute of Science Bangalore · IN

Funding

UNM Initiative to Maximize Student Diversity (IMSD)R25GM060201 · NIGMS · UNIVERSITY OF NEW MEXICO · PI WERNER-WASHBURNE, MARGRET C. · 2000 to 2017
$9.9M
Genetic regulation of cell fate in the Drosophila heartR01HL080545 · NHLBI · UNIVERSITY OF NEW MEXICO · PI CRIPPS, RICHARD MATTHEW · 2005 to 2009
$1.3M
NHLBI NIH HHS R01 HL080545NIGMS NIH HHS R25 GM060201
6 · The paper itself

Abstract

Understanding the basis of normal heart remodeling can provide insight into the plasticity of the cardiac state, and into the potential for treating diseased tissue. In Drosophila, the adult heart arises during metamorphosis from a series of events, that include the remodeling of an existing cardiac tube, the elaboration of new inflow tracts, and the addition of a layer of longitudinal muscle fibers. We have identified genes active in all these three processes, and studied their expression in order to characterize in greater detail normal cardiac remodeling. Using a Transglutaminase-lacZ transgenic line, that is expressed in the inflow tracts of the larval and adult heart, we confirm the existence of five inflow tracts in the adult structure. In addition, expression of the Actin87E actin gene is initiated in the remodeling cardiac tube, but not in the longitudinal fibers, and we have identified an Act87E promoter fragment that recapitulates this switch in expression. We also establish that the longitudinal fibers are multinucleated, characterizing these cells as specialized skeletal muscles. Furthermore, we have defined the origin of the longitudinal fibers, as a subset of lymph gland cells associated with the larval dorsal vessel. These studies underline the myriad contributors to the formation of the adult Drosophila heart, and provide new molecular insights into the development of this complex organ.

Indexed as

Cardiovascular Physiological PhenomenaGene Expression Regulation, DevelopmentalActinsAnimalsAnimals, Genetically ModifiedAntigens, Differentiationbeta-GalactosidaseCell TransdifferentiationDrosophilaDrosophila ProteinsGATA Transcription FactorsGenes, ReporterHeartLymphoid TissueMuscle, SkeletalMyocardiumActinsAntigens, Differentiationbeta-GalactosidaseDrosophila ProteinsGATA Transcription FactorsMef2 protein, DrosophilaMyogenic Regulatory Factorssrp protein, Drosophila

Identifiers

PMID21237266
PMCPMC3065548
OpenAlexW2058004965

What OpenQuestion holds

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Registered trials

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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.