Evidence map›Paper›PMID 26443637›Full record

ArticleDevelopment (Cambridge, England)2015

Cell type-specific translational repression of Cyclin B during meiosis in males.

Catherine Craig Baker, Byung Soo Gim, Margaret T Fuller

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

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  17. Single-cyst transcriptome analysis ofDevelopment (Cambridge, England) · 2020
    Article
  18. Article
  19. Development (Cambridge, England) · 2019
    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

3 authors at 1 institution in 1 country.

Catherine Craig BakerDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305-5329, USA.
Byung Soo GimDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305-5329, USA.
Margaret T FullerDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305-5329, USA Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305-5329, USA mtfuller@stanford.edu.
Stanford University · US

Funding

Stanford University Center for Reproductive and Stem Cell biologyU54HD068158 · NICHD · STANFORD UNIVERSITY · PI HSUEH, AARON · 2011 to 2013
$5.0M
Stanford University Center for Reproductive and Stem Cell biologyP50HD068158 · NICHD · STANFORD UNIVERSITY · PI FULLER, MARGARET T · 2014 to 2015
$3.3M
NICHD NIH HHS P50 HD068158NICHD NIH HHS U54 HD068158
6 · The paper itself

Abstract

The unique cell cycle dynamics of meiosis are controlled by layers of regulation imposed on core mitotic cell cycle machinery components by the program of germ cell development. Although the mechanisms that regulate Cdk1/Cyclin B activity in meiosis in oocytes have been well studied, little is known about the trans-acting factors responsible for developmental control of these factors in male gametogenesis. During meiotic prophase in Drosophila males, transcript for the core cell cycle protein Cyclin B1 (CycB) is expressed in spermatocytes, but the protein does not accumulate in spermatocytes until just before the meiotic divisions. Here, we show that two interacting proteins, Rbp4 and Fest, expressed at the onset of spermatocyte differentiation under control of the developmental program of male gametogenesis, function to direct cell type- and stage-specific repression of translation of the core G2/M cell cycle component cycB during the specialized cell cycle of male meiosis. Binding of Fest to Rbp4 requires a 31-amino acid region within Rbp4. Rbp4 and Fest are required for translational repression of cycB in immature spermatocytes, with Rbp4 binding sequences in a cell type-specific shortened form of the cycB 3' UTR. Finally, we show that Fest is required for proper execution of meiosis I.

Indexed as

AnimalsAnimals, Genetically ModifiedBlotting, WesternCloning, MolecularCRISPR-Cas SystemsCyclin BDNA PrimersDrosophilaDrosophila ProteinsGene Expression Regulation, DevelopmentalImmunoprecipitationMaleMeiosisMicroscopy, FluorescenceReverse Transcriptase Polymerase Chain ReactionRNA Polymerase IICyclin BDNA PrimersDrosophila ProteinsRNA Polymerase IIRPB4 protein, DrosophilaCyclin BDrosophilaMeiosisSpermatogenesisTranslational control

Identifiers

PMID26443637
PMCPMC4631753
OpenAlexW2248241623

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.