Evidence map›Paper›PMID 22927345›Full record

ReviewCytoskeleton (Hoboken, N.J.)2012

What Drosophila spermatocytes tell us about the mechanisms underlying cytokinesis.

Maria Grazia Giansanti, Margaret T Fuller

Abstract readReview
In one paragraph

Review in Cytoskeleton (Hoboken, N.J.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  4. Review
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  9. Review
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  11. TheCells · 2020
    Article
  12. Profilin choreographs actin and microtubules in cells and cancer.International review of cell and molecular biology · 2020
    Article
  13. Development (Cambridge, England) · 2019
    Article
  14. Article
  15. Article
  16. COG7 deficiency inJournal of cell science · 2017
    Article
  17. Article
  18. Article
  19. Article
  20. Article
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 2 countries.

Maria Grazia GiansantiIstituto di Biologia e Patologia Molecolari del CNR, Dipartimento di Biologia e Biotecnologie Università Sapienza di Roma, Piazzale A. Moro 5, Roma, Italy. Mariagrazia.Giansanti@uniroma1.it
Margaret T Fuller
Stanford University · US

Funding

Stanford University Center for Reproductive and Stem Cell biologyU54HD068158 · NICHD · STANFORD UNIVERSITY · PI FULLER, MARGARET T · 2011 to 2013
$5.0M
Regulation of Stem Cell Self-Renewal and DifferentiationR01GM080501 · NIGMS · STANFORD UNIVERSITY · PI FULLER, MARGARET T · 2007 to 2019
$3.8M
NICHD NIH HHS U54 HD068158NIGMS NIH HHS R01 GM080501
6 · The paper itself

Abstract

Cytokinesis separates the genomic material and organelles of a dividing cell equitably into two physically distinct daughter cells at the end of cell division. This highly choreographed process involves coordinated reorganization and regulated action of the actin and microtubule cytoskeletal systems, an assortment of motor proteins, and membrane trafficking components. Due to their large size, the ease with which exquisite cytological analysis may be performed on them, and the availability of numerous mutants and other genetic tools, Drosophila spermatocytes have provided an excellent system for exploring the mechanistic basis for the temporally programmed and precise spatially localized events of cytokinesis. Mutants defective in male meiotic cytokinesis can be easily identified in forward genetic screens by the production of multinucleate spermatids. In addition, the weak spindle assembly checkpoint in spermatocytes, which causes only a small delay of anaphase onset in the presence of unattached chromosomes, allows investigation of whether gene products required for spindle assembly and chromosome segregation are also involved in cytokinesis. Perhaps due to the large size of spermatocytes and the requirement for two rapid-fire rounds of division without intervening S or growth phases during meiosis, male meiotic mutants have also revealed much about molecular mechanisms underlying new membrane addition during cytokinesis. Finally, cell type-specific differences in the events that set up and complete cytokinesis are emerging from comparison of spermatocytes with cells undergoing mitosis either elsewhere in the organism or in tissue culture.

Indexed as

AnimalsCell Cycle CheckpointsCytokinesisDrosophila melanogasterMaleMeiosisMutationSpermatocytesSpindle Apparatus

Identifiers

PMID22927345
PMCPMC4165571
OpenAlexW2048435228

What OpenQuestion holds

Textmetadata
LicenceTDM
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.