Evidence map›Paper›PMID 37882771›Full record

ArticleDevelopment (Cambridge, England)2023

Cell-type-specific interacting proteins collaborate to regulate the timing of Cyclin B protein expression in male meiotic prophase.

Catherine C Baker, Lorenzo Gallicchio, Neuza R Matias, Douglas F Porter, Lucineh Parsanian, Emily Taing, Cheuk Tam, Margaret T Fuller

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Catherine C BakerDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-6225-7632
Lorenzo GallicchioDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-5040-0139
Neuza R MatiasDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0003-1548-037X
Douglas F PorterProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0001-9491-8258
Lucineh ParsanianDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-1401-4337
Emily TaingDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0003-4689-134X
Cheuk TamDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0001-9932-8396
Margaret T FullerDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-3804-4987
Stanford University · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Vittorio Sebastiano · 2007 to 2026
$71.4M
Regulation of proliferation and differentiation in the male germ line adult stem cell lineageR35GM136433 · NIGMS · STANFORD UNIVERSITY · PI MARGARET T FULLER · 2020 to 2026
$5.9M
Developmental Control of the Cell Cycle in Male MeiosisR01GM081802 · NIGMS · STANFORD UNIVERSITY · PI FULLER, MARGARET T · 2007 to 2010
$1.1M
Developmentally programmed translational control of specialized cell cycles in male meiosisR01GM124054 · NIGMS · STANFORD UNIVERSITY · PI FULLER, MARGARET T · 2018 to 2019
$628k
REGULATION OF SKIN HOMEOSTASIS BY RNA-BINDING PROTEINSK01AR082351 · NIAMS · STANFORD UNIVERSITY · PI PORTER, DOUGLAS F · 2023 to 2025
$369k
NCI NIH HHS P30 CA124435NIAMS NIH HHS K01 AR082351NIGMS NIH HHS R01 GM081802NIGMS NIH HHS R01 GM124054NIGMS NIH HHS R35 GM136433NIH HHS R35GM136433
6 · The paper itself

Abstract

During meiosis, germ cell and stage-specific components impose additional layers of regulation on the core cell cycle machinery to set up an extended G2 period termed meiotic prophase. In Drosophila males, meiotic prophase lasts 3.5 days, during which spermatocytes upregulate over 1800 genes and grow 25-fold. Previous work has shown that the cell cycle regulator Cyclin B (CycB) is subject to translational repression in immature spermatocytes, mediated by the RNA-binding protein Rbp4 and its partner Fest. Here, we show that the spermatocyte-specific protein Lut is required for translational repression of cycB in an 8-h window just before spermatocytes are fully mature. In males mutant for rbp4 or lut, spermatocytes enter and exit meiotic division 6-8 h earlier than in wild type. In addition, spermatocyte-specific isoforms of Syncrip (Syp) are required for expression of CycB protein in mature spermatocytes and normal entry into the meiotic divisions. Lut and Syp interact with Fest independent of RNA. Thus, a set of spermatocyte-specific regulators choreograph the timing of expression of CycB protein during male meiotic prophase.

Indexed as

Drosophila ProteinsMeiosisAnimalsCyclin BDrosophilaMaleMitosisProphaseSpermatocytesSpermatogenesisCycB protein, DrosophilaCyclin BDrosophila ProteinsCyclin BDrosophilaMeiosisRNASpermatogenesisTranslation

Identifiers

PMID37882771
PMCPMC10730016
OpenAlexW4387949993

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.