Evidence map›Paper›PMID 30763280›Full record

ArticleReproduction (Cambridge, England)2018

Cyclin-dependent kinase 21 is a novel regulator of proliferation and meiosis in the male germline of zebrafish.

Kaitlyn A Webster, Katrin Henke, Delaney M Ingalls, Adeeba Nahrin, Matthew P Harris, Kellee R Siegfried

Open access · bronzeAbstract read
In one paragraph

Article in Reproduction (Cambridge, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Evolution of the Cdk4/6-Cdkn2 system in invertebrates.Genes to cells : devoted to molecular & cellular mechanisms · 2024
    Article
  3. Article
  4. Article
  5. Sexual determination in zebrafish.Cellular and molecular life sciences : CMLS · 2021
    Review
  6. Review
  7. Article
  8. Article
  9. Loss ofDevelopment (Cambridge, England) · 2020
    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

6 authors at 4 institutions in 1 country.

Kaitlyn A WebsterBiology Department, University of Massachusetts Boston, Boston, Massachusetts, USA.
Katrin HenkeOrthopaedic Research Laboratories, Boston Children's Hospital and Department of Genetics, Harvard Medical School, Boston, Massachusetts, USA.
Delaney M IngallsBiology Department, University of Massachusetts Boston, Boston, Massachusetts, USA.
Adeeba NahrinBiology Department, University of Massachusetts Boston, Boston, Massachusetts, USA.
Matthew P HarrisOrthopaedic Research Laboratories, Boston Children's Hospital and Department of Genetics, Harvard Medical School, Boston, Massachusetts, USA.
Kellee R SiegfriedBiology Department, University of Massachusetts Boston, Boston, Massachusetts, USA.
University of Massachusetts Boston · USBoston Children's Hospital · USBoston University · USHarvard University · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI Irene M. Ghobrial · 1985 to 2026
$330.6M
UMass Boston-DF/HCC U54 Partnership (2 of 2)U54CA156734 · NCI · UNIVERSITY OF MASSACHUSETTS BOSTON · PI Jan Mutchler · 2010 to 2026
$24.9M
Initiative for Maximizing Student Diversity at UMass BostonR25GM076321 · NIGMS · UNIVERSITY OF MASSACHUSETTS BOSTON · PI COLON-CARMONA, ADAN, SKVIRSKY, RACHEL · 2008 to 2022
$4.5M
Identification of genetic factors contributing to germline stem cell maintenanceR03HD097433 · NICHD · UNIVERSITY OF MASSACHUSETTS BOSTON · PI HENKE, KATRIN, SIEGFRIED, KELLEE R · 2019 to 2020
$171k
NCI NIH HHS P30 CA006516NCI NIH HHS U54 CA156734NICHD NIH HHS R03 HD097433NIGMS NIH HHS R25 GM076321
6 · The paper itself

Abstract

Germ cell differentiation and maintenance relies on complex regulation of mitotic and meiotic progression. Cyclin-dependent kinases (CDKs) and their activating cyclin partners are known to have specialized roles in regulating cell cycle progression across tissues, including germ cells. Very little is known about CDK/cyclin function in zebrafish or the regulation of germ cell maintenance and differentiation. In a forward genetic screen for gonadogenesis defects in zebrafish, a mutation disrupting cdk21 (cyclin-dependent kinase 21) was identified, which caused gonad hypoplasia, reduced fertility and failure of female sex specification. The cdk21 gene is unique to fishes, though the encoded protein is related to the D-cyclin partners Cdk4 and Cdk6, which are known G1 cell cycle regulators. In the testis, cdk21 mutant germ cells exhibited cell cycle defects such as diminished proliferation, prolonged meiosis and delayed sperm differentiation. Furthermore, cdk21 mutants failed to maintain germ cells following breeding. Based on these findings, we propose that cdk21 regulates spermatogonial proliferation, progression through meiosis and germline stem cell activation in the testis. In addition, we investigated cdk4 and cdk6 in zebrafish development and found that each has distinct expression patterns in the gonads. Mutant analysis demonstrated that cdk6 was necessary for viability beyond larval stages. In contrast, cdk4 mutants were viable but were all male with low breeding success and sperm overabundance. Our analysis demonstrated that zebrafish harbor three genes of the cdk4/6 family, cdk4, cdk6 and cdk21, with cdk21 having an essential role in germ cell development in the testis.

Indexed as

Cell ProliferationMeiosisAnimalsCyclin-Dependent KinasesCyclinsFemaleG1 PhaseGerm CellsMaleOogenesisPhosphorylationSpermatogenesisZebrafishZebrafish ProteinsCyclin-Dependent KinasesCyclinsZebrafish Proteins

Identifiers

PMID30763280
PMCPMC6489137
OpenAlexW2914635326

What Socratic 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 Socratic graph.