Evidence map›Paper›PMID 18493084›Full record

ArticleGenetics2008

Genetic characterization of the Drosophila jaguar322 mutant reveals that complete myosin VI loss of function is not lethal.

Julie K Morrison, Kathryn G Miller

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Myosin VI is expressed in developing ovarian follicles inFrontiers in cell and developmental biology · 2025
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  4. Review
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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

2 authors at 1 institution in 1 country.

Julie K MorrisonDepartment of Biology, Washington University, St. Louis, MO 63130, USA.
Kathryn G Miller
Washington University in St. Louis · US

Funding

Myosin VI in Intracellular Transport/LocalizationR01GM060494 · NIGMS · WASHINGTON UNIVERSITY · PI MILLER, KATHRYN G · 2000 to 2011
$4.1M
NIGMS NIH HHS GM-060494NIGMS NIH HHS R01 GM060494
6 · The paper itself

Abstract

Myosin VI is an actin-based motor that has been implicated in many cellular processes. Studies in vertebrates have demonstrated that animals lacking this ubiquitously expressed myosin are viable. However in Drosophila, myosin VI loss of function has been thought to be lethal. We show here that complete loss of myosin VI is not lethal in flies and that the previously reported lethality of the null mutation (jar322) is most likely due to deletion of a neighboring gene. Maternally provided myosin VI does not account for the survival of myosin VI null animals. Mutant animals are recovered at a lower than expected Mendelian frequency, suggesting that myosin VI participates in processes which contribute to normal development, but its participation is not essential.

Indexed as

AnimalsBlotting, WesternDNA PrimersDrosophila melanogasterGene ComponentsGenetic Complementation TestMicroscopy, FluorescenceMutationMyosin Heavy ChainsReverse Transcriptase Polymerase Chain ReactionDNA PrimersMyosin Heavy Chainsmyosin VI

Identifiers

PMID18493084
PMCPMC2390649
OpenAlexW1969317867

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.