Evidence map›Paper›PMID 39614055›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Studying Mitotic Phosphorylation in Drosophila.

Éric Bonneil, Myreille Larouche, Virginie Emond-Fraser, Peter Kubiniok, Cristina Mirela Pascariu, Pierre Thibault, Vincent Archambault

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Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Éric BonneilInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
Myreille LaroucheInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
Virginie Emond-FraserInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
Peter KubiniokInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
Cristina Mirela PascariuInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
Pierre ThibaultInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada.
Vincent ArchambaultInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, QC, Canada. vincent.archambault.1@umontreal.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitosis is largely controlled by the reversible phosphorylation of effector proteins. The addition or removal of phosphate groups alters the activities of these proteins, resulting in changes in chromosome structure, cytoskeletal dynamics, nuclear envelope integrity, and other transformations that must occur as a cell progresses through mitosis. Drosophila has been instrumental in the elucidation of the molecular mechanisms of mitosis, which are mostly conserved among animals. In this model system, sophisticated genetic tools can be used to study mitosis in different tissues during development in vivo. Drosophila cell culture affords complementary possibilities. In this chapter, we present a phosphoproteomic protocol using Drosophila cell culture to identify phosphorylation sites that depend on mitotic kinases and phosphatases. We also provide protocols to dissect the roles of the identified sites in the regulation of protein interactions and localization during mitosis, using Drosophila embryos. We emphasize the advantages of the selected methods compared to possible alternatives in Drosophila or in other systems.

Indexed as

MitosisAnimalsDrosophilaDrosophila melanogasterDrosophila ProteinsPhosphoproteinsPhosphorylationProteomicsDrosophila ProteinsPhosphoproteinsBiochemistryCell biologyDrosophilaMicroscopyMitosisPhosphorylationProteomics

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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.