Evidence map›Paper›PMID 33248112›Full record

ArticleDevelopmental biology2021

Mutations in Drosophila crinkled/Myosin VIIA disrupt denticle morphogenesis.

Jennifer L Sallee, Janice M Crawford, Vinay Singh, Daniel P Kiehart

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. The filopodial myosin DdMyo7 is a slow, calcium-regulated motor.The Journal of biological chemistry · 2025
    Article
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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

4 authors at 1 institution in 1 country.

Jennifer L SalleeDepartment of Biology, Duke University, Durham, NC, 27708, USA; Department of Biology, North Central College, Naperville, IL, 60540, USA. Electronic address: jlsallee@noctrl.edu.
Janice M CrawfordDepartment of Biology, Duke University, Durham, NC, 27708, USA.
Vinay SinghDepartment of Biology, Duke University, Durham, NC, 27708, USA.
Daniel P KiehartDepartment of Biology, Duke University, Durham, NC, 27708, USA. Electronic address: dkiehart@duke.edu.
Duke University · US

Funding

Morphogenesis: Biophysics and Genetics of Dorsal ClosureR01GM033830 · NIGMS · HARVARD UNIVERSITY · PI KIEHART, DANIEL PETER · 1985 to 2017
$7.2M
Morphogenesis: Biophysics and Genetics of Dorsal ClosureR35GM127059 · NIGMS · DUKE UNIVERSITY · PI DANIEL PETER KIEHART · 2018 to 2026
$4.5M
Myosins VIIA, VIIB &XV in Fly Hearing and MorphogenesisR01DC007673 · NIDCD · DUKE UNIVERSITY · PI KIEHART, DANIEL PETER · 2005 to 2009
$1.7M
Actin protrustions, oocytes: Myosin VIIA and the actin cytoskeletonF32GM093592 · NIGMS · DUKE UNIVERSITY · PI SALLEE, JENNIFER LEIGH · 2010 to 2012
$153k
NIDCD NIH HHS R01 DC007673NIGMS NIH HHS F32 GM093592NIGMS NIH HHS R01 GM033830NIGMS NIH HHS R35 GM127059
6 · The paper itself

Abstract

Actin filament crosslinking, bundling and molecular motor proteins are necessary for the assembly of epithelial projections such as microvilli, stereocilia, hairs, and bristles. Mutations in such proteins cause defects in the shape, structure, and function of these actin - based protrusions. One protein necessary for stereocilia formation, Myosin VIIA, is an actin - based motor protein conserved throughout phylogeny. In Drosophila melanogaster, severe mutations in the MyoVIIA homolog crinkled (ck) are "semi - lethal" with only a very small percentage of flies surviving to adulthood. Such survivors show morphological defects related to actin bundling in hairs and bristles. To better understand ck/MyoVIIA's function in bundled - actin structures, we used dominant female sterile approaches to analyze the loss of maternal and zygotic (M/Z) ck/MyoVIIA in the morphogenesis of denticles, small actin - based projections on the ventral epidermis of Drosophila embryos. M/Z ck mutants displayed severe defects in denticle morphology - actin filaments initiated in the correct location, but failed to elongate and bundle to form normal projections. Using deletion mutant constructs, we demonstrated that both of the C - terminal MyTH4 and FERM domains are necessary for proper denticle formation. Furthermore, we show that ck/MyoVIIA interacts genetically with dusky - like (dyl), a member of the ZPD family of proteins that links the extracellular matrix to the plasma membrane, and when mutated also disrupts normal denticle formation. Loss of either protein alone does not alter the localization of the other; however, loss of the two proteins together dramatically enhances the defects in denticle shape observed when either protein alone was absent. Our data indicate that ck/MyoVIIA plays a key role in the formation and/or organization of actin filament bundles, which drive proper shape of cellular projections.

Indexed as

Actin CytoskeletonAnimalsCell Surface ExtensionsDrosophila melanogasterDrosophila ProteinsEpidermisFemaleMaleMembrane ProteinsMorphogenesisMutant ProteinsMutationMyosin VIIack protein, DrosophilaDrosophila ProteinsDyl protein, DrosophilaMembrane ProteinsMutant ProteinsMyosin VIIaActin-based projectionsActin cytoskeletonDenticlesDrosophilaMyosin VIIA

Identifiers

PMID33248112
PMCPMC7855556
OpenAlexW3110357783

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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.