Evidence map›Paper›PMID 21624359›Full record

ArticleDevelopmental biology2011

The E3 ubiquitin ligase Cullin 4A regulates meiotic progression in mouse spermatogenesis.

Yan Yin, Congxing Lin, Sung Tae Kim, Ignasi Roig, Hong Chen, Liren Liu, George Michael Veith, Ramon U Jin, Scott Keeney, Maria Jasin and 3 more

Abstract read
In one paragraph

Article in Developmental biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

54 citing papers in PubMed, 82 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. A Z-Linked E3 Ubiquitin LigaseAnimals : an open access journal from MDPI · 2021
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. The testis-specifically expressed geneJournal of biomedical research · 2020
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 2 countries.

Yan YinDivision of Dermatology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Congxing Lin
Sung Tae Kim
Ignasi Roig
Hong Chen
Liren Liu
George Michael Veith
Ramon U Jin
Scott Keeney
Maria Jasin
Kelle Moley
Pengbo Zhou
Liang Ma
Washington University in St. Louis · USCornell University · USMemorial Sloan Kettering Cancer Center · USUniversitat Autònoma de Barcelona · ES

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Regulation of Nucleotide Excision Repair by ProteolysisR01CA098210 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI ZHOU, PENGBO · 2003 to 2013
$3.3M
Institute for Translational Health Science (TL1)TL1RR025016 · NCRR · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2007 to 2011
$2.7M
DES and the Regulation of the Uterine CytodifferentiationR01ES014482 · NIEHS · WASHINGTON UNIVERSITY · PI MA, LIANG · 2006 to 2010
$1.8M
EXTERNAL GENITALIA DEVELOPMENT AND HYPOSPADIASR01ES016597 · NIEHS · WASHINGTON UNIVERSITY · PI MA, LIANG · 2009 to 2013
$1.5M
Ubiquitin-Proteolytic Control of HOXA9 in LeukemogenesisR01CA118085 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI ZHOU, PENGBO · 2006 to 2010
$1.5M
Regulation of Nucleotide Excision Repair by ProteolysisR56CA098210 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI ZHOU, PENGBO · 2008 to 2008
$329k
NCI NIH HHS CA098210NCI NIH HHS CA118085NCI NIH HHS P30 CA091842NCI NIH HHS P30 CA91842NCI NIH HHS R01 CA098210NCI NIH HHS R01 CA118085NCI NIH HHS R56 CA098210NCRR NIH HHS TL1 RR025016NIEHS NIH HHS ES014482NIEHS NIH HHS ES016597NIEHS NIH HHS R01 ES014482NIEHS NIH HHS R01 ES016597
6 · The paper itself

Abstract

The Cullin-RING ubiquitin-ligase CRL4 controls cell cycle and DNA damage checkpoint response and ensures genomic integrity. Inactivation of the Cul4 component of the CRL4 E3 ligase complex in Caenorhabditis elegans by RNA interference results in massive mitotic DNA re-replication in the blast cells, largely due to failed degradation of the DNA licensing protein, CDT-1, and premature spermatogenesis. Here we show that inactivation of Cul4a by gene-targeting in mice only affected male but not female fertility. This male infertility phenotype resulted from a combination of decreased spermatozoa number, reduced sperm motility and defective acrosome formation. Agenesis of the mutant germ cells was accompanied by increased cell death in pachytene/diplotene cells with markedly elevated levels of phospho-p53 and CDT-1. Despite apparent normal assembly of synaptonemal complexes and DNA double strand break repair, dissociation of MLH1, a component of the late recombination nodule, was delayed in Cul4a -/- diplotene spermatocytes, which potentially led to subsequent disruptions in meiosis II and spermiogenesis. Together, our study revealed an indispensable role for Cul4a during male germ cell meiosis.

Indexed as

AcrosomeAdaptor Proteins, Signal TransducingAnimalsCell DeathCullin ProteinsDNA Breaks, Double-StrandedDNA RepairInfertility, MaleMaleMeiosisMiceMice, TransgenicMutL Protein Homolog 1Nuclear ProteinsPhosphoproteinsSpermatocytesAdaptor Proteins, Signal TransducingCul4a protein, mouseCullin ProteinsMlh1 protein, mouseMutL Protein Homolog 1Nuclear ProteinsPhosphoproteinsTumor Suppressor Protein p53

Identifiers

PMID21624359
PMCPMC3130830
OpenAlexW2107945594

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.