Evidence map›Paper›PMID 18678708›Full record

ArticleThe Journal of cell biology2008

Bat3 deficiency accelerates the degradation of Hsp70-2/HspA2 during spermatogenesis.

Toru Sasaki, Edyta Marcon, Tracy McQuire, Yoichi Arai, Peter B Moens, Hitoshi Okada

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

27 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  6. A noncanonical role of NOD-like receptor NLRP14 in PGCLC differentiation and spermatogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  7. Article
  8. Article
  9. Hijacking of the Host Ubiquitin Network byFrontiers in cellular and infection microbiology · 2017
    Review
  10. Article
  11. Review
  12. Malfunction of spermatogenesis in experimental ischemic mice.The Journal of reproduction and development · 2015
    Article
  13. Article
  14. Article
  15. BAG-6, a jack of all trades in health and disease.Cellular and molecular life sciences : CMLS · 2014
    Review
  16. Bag6/Bat3/Scythe: a novel chaperone activity with diverse regulatory functions in protein biogenesis and degradation.BioEssays : news and reviews in molecular, cellular and developmental biology · 2013
    Review
  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

6 authors at 3 institutions in 3 countries.

Toru SasakiThe Campbell Family Institute for Breast Cancer Research, Ontario Cancer Institute, University Health Network, University of Toronto, Toronto, Ontario M5G2C1, Canada.
Edyta Marcon
Tracy McQuire
Yoichi Arai
Peter B Moens
Hitoshi Okada
York University · CATohoku University · JPUniversity of Toronto · CA

Funding

PROJECT 3 - Steroid-Metabolic Interactions In the Control of GnRH NeuronsU54HD028934 · NICHD · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI MARSHALL, JOHN C · 1998 to 2013
$16.5M
NICHD NIH HHS U54 HD028934NICHD NIH HHS U54-HD28934
6 · The paper itself

Abstract

Meiosis is critical for sexual reproduction. During meiosis, the dynamics and integrity of homologous chromosomes are tightly regulated. The genetic and molecular mechanisms governing these processes in vivo, however, remain largely unknown. In this study, we demonstrate that Bat3/Scythe is essential for survival and maintenance of male germ cells (GCs). Targeted inactivation of Bat3/Scythe in mice results in widespread apoptosis of meiotic male GCs and complete male infertility. Pachytene spermatocytes exhibit abnormal assembly and disassembly of synaptonemal complexes as demonstrated by abnormal SYCP3 staining and sustained gamma-H2AX and Rad51/replication protein A foci. Further investigation revealed that a testis-specific protein, Hsp70-2/HspA2, is absent in Bat3-deficient male GCs at any stage of spermatogenesis; however, Hsp70-2 transcripts are expressed at normal levels. We found that Bat3 deficiency induces polyubiquitylation and subsequent degradation of Hsp70-2. Inhibition of proteasomal degradation restores Hsp70-2 protein levels. Our findings identify Bat3 as a critical regulator of Hsp70-2 in spermatogenesis, thereby providing a possible molecular target in idiopathic male infertility.

Indexed as

Protein Processing, Post-TranslationalSpermatogenesisAnimalsApoptosisCarrier ProteinsCell LineHSP70 Heat-Shock ProteinsHumansMaleMiceMolecular ChaperonesNuclear ProteinsOrgan SpecificityPolyubiquitinProtein BindingSpermatozoaBag6 protein, mouseCarrier ProteinsHSP70 Heat-Shock ProteinsHspa2 protein, mouseMolecular ChaperonesNuclear ProteinsPolyubiquitin

Identifiers

PMID18678708
PMCPMC2500131
OpenAlexW2151865869

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.