Evidence map›Paper›PMID 28117804›Full record

ArticleJournal of visualized experiments : JoVE2017

Studying Mitochondrial Structure and Function in Drosophila Ovaries.

Danitra J Parker, Aida Moran, Kasturi Mitra

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2017. 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
0.4field-weighted citation impact, top 38% 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, 13 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Danitra J ParkerDepartment of Genetics, School of Medicine, University of Alabama at Birmingham.
Aida MoranDepartment of Genetics, School of Medicine, University of Alabama at Birmingham.
Kasturi MitraDepartment of Genetics, School of Medicine, University of Alabama at Birmingham; kasturi@uab.edu.
University of Alabama at Birmingham · US

Funding

RT-SQuARED-M method to study the precise role of mitochondria in the oxidative damage caused by environmental toxinsR33ES025662 · NIEHS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MITRA, KASTURI · 2018 to 2019
$1.1M
RT-SQuARED-M method to study the precise role of mitochondria in the oxidative damage caused by environmental toxinsR21ES025662 · NIEHS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MITRA, KASTURI · 2015 to 2017
$549k
NIEHS NIH HHS R21 ES025662NIEHS NIH HHS R33 ES025662
6 · The paper itself

Abstract

Analysis of the mitochondrial structure-function relationship is required for a thorough understanding of the regulatory mechanisms of mitochondrial functionality. Fluorescence microscopy is an indispensable tool for the direct assessment of mitochondrial structure and function in live cells and for studying the mitochondrial structure-function relationship, which is primarily modulated by the molecules governing fission and fusion events between mitochondria. This paper describes and demonstrates specific methods for studying mitochondrial structure and function in live as well as in fixed tissue in the model organism Drosophila melanogaster. The tissue of choice here is the Drosophila ovary, which can be isolated and made amenable for ex vivo live confocal microscopy. Furthermore, the paper describes how to genetically manipulate the mitochondrial fission protein, Drp1, in Drosophila ovaries to study the involvement of Drp1-driven mitochondrial fission in modulating the mitochondrial structure-function relationship. The broad use of such methods is demonstrated in already-published as well as in novel data. The described methods can be further extended towards understanding the direct impact of nutrients and/or growth factors on the mitochondrial properties ex vivo. Given that mitochondrial dysregulation underlies the etiology of various diseases, the described innovative methods developed in a genetically tractable model organism, Drosophila, are anticipated to contribute significantly to the understanding of the mechanistic details of the mitochondrial structure-function relationship and to the development of mitochondria-directed therapeutic strategies.

Indexed as

AnimalsCyclin ECytoskeletal ProteinsDrosophilaFemaleGTP-Binding ProteinsMicroscopy, ConfocalMitochondriaMitochondrial DynamicsMitochondrial ProteinsOvaryPhotobleachingCyclin ECytoskeletal ProteinsDRP1 protein, DrosophilaGTP-Binding ProteinsMitochondrial Proteins

Identifiers

PMID28117804
PMCPMC6622407
OpenAlexW2570065601

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.