Evidence map›Paper›PMID 21179520›Full record

ArticlePloS one2010

Regulation and functions of the lms homeobox gene during development of embryonic lateral transverse muscles and direct flight muscles in Drosophila.

Dominik Müller, Teresa Jagla, Ludivine Mihaila Bodart, Nina Jährling, Hans-Ulrich Dodt, Krzysztof Jagla, Manfred Frasch

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  3. Misregulation ofFrontiers in neural circuits · 2021
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  8. COG7 deficiency inJournal of cell science · 2017
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  12. Article
  13. Specification of the somatic musculature in Drosophila.Wiley interdisciplinary reviews. Developmental biology
    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

7 authors at 4 institutions in 4 countries.

Dominik MüllerDivision of Developmental Biology, Department of Biology, University of Erlangen-Nuremberg, Erlangen, Germany.
Teresa Jagla
Ludivine Mihaila Bodart
Nina Jährling
Hans-Ulrich Dodt
Krzysztof Jagla
Manfred Frasch
Friedrich-Alexander-Universität Erlangen-Nürnberg · DETU Wien · ATUniversité Clermont Auvergne · FRIcahn School of Medicine at Mount Sinai · US

Funding

REGULATION OF MESODERM DEVELOPMENTR01HD030832 · NICHD · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI FRASCH, MANFRED · 1994 to 2008
$2.8M
NICHD NIH HHS HD30832NICHD NIH HHS R01 HD030832
6 · The paper itself

Abstract

backgroundPatterning and differentiation of developing musculatures require elaborate networks of transcriptional regulation. In Drosophila, significant progress has been made into identifying the regulators of muscle development and defining their interactive networks. One major family of transcription factors involved in these processes consists of homeodomain proteins. In flies, several members of this family serve as muscle identity genes to specify the fates of individual muscles, or groups thereof, during embryonic and/or adult muscle development. Herein, we report on the expression and function of a new Drosophila homeobox gene during both embryonic and adult muscle development. METHODOLOGY/PRINCIPAL

findingsThe newly described homeobox gene, termed lateral muscles scarcer (lms), which has yet uncharacterized orthologs in other invertebrates and primitive chordates but not in vertebrates, is expressed exclusively in subsets of developing muscle tissues. In embryos, lms is expressed specifically in the four lateral transverse (LT) muscles and their founder cells in each hemisegment, whereas in larval wing imaginal discs, it is expressed in myoblasts that develop into direct flight muscles (DFMs), which are important for proper wing positioning. We have analyzed the regulatory inputs of various other muscle identity genes with overlapping or complementary expression patterns towards the cell type specific regulation of lms expression. Further we demonstrate that lms null mutants exhibit reduced numbers of embryonic LT muscles, and null mutant adults feature held-out-wing phenotypes. We provide a detailed description of the pattern and morphology of the direct flight muscles in the wild type and lms mutant flies by using the recently-developed ultramicroscopy and show that, in the mutants, all DFMs are present and present normal morphologies. CONCLUSIONS/SIGNIFICANCE: We have identified the homeobox gene lms as a new muscle identity gene and show that it interacts with various previously-characterized muscle identity genes to regulate normal formation of embryonic lateral transverse muscles. In addition, the direct flight muscles in the adults require lms for reliably exerting their functions in controlling wing postures.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsBody PatterningCrosses, GeneticDrosophila melanogasterDrosophila ProteinsFlight, AnimalGene DeletionGenes, HomeoboxHomeodomain ProteinsModels, GeneticMusclesMutationPhenotypeWings, AnimalDrosophila ProteinsHomeodomain Proteins

Identifiers

PMID21179520
PMCPMC3002276
OpenAlexW1985213036

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.