Evidence map›Paper›PMID 26490168›Full record

ArticleChromosoma2016

FancJ (Brip1) loss-of-function allele results in spermatogonial cell depletion during embryogenesis and altered processing of crossover sites during meiotic prophase I in mice.

Xianfei Sun, Miguel A Brieño-Enríquez, Alyssa Cornelius, Andrew J Modzelewski, Tyler T Maley, Kadeine M Campbell-Peterson, J Kim Holloway, Paula E Cohen

Open access · greenAbstract read
In one paragraph

Article in Chromosoma, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Seasonal piRNA Expression Profile Changes in the Testes of Plateau Zokor (Animals : an open access journal from MDPI · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Cell genomics · 2023
    Article
  9. Review
  10. Observational
  11. Review
  12. Article
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  14. Article
  15. Article
  16. Article
  17. 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

8 authors at 2 institutions in 1 country.

Xianfei SunDepartment of Biomedical Sciences and Center for Reproductive Genomics, Cornell University, Tower Road, Ithaca, NY, 14853, USA.
Miguel A Brieño-EnríquezDepartment of Biomedical Sciences and Center for Reproductive Genomics, Cornell University, Tower Road, Ithaca, NY, 14853, USA.
Alyssa CorneliusDepartment of Biomedical Sciences and Center for Reproductive Genomics, Cornell University, Tower Road, Ithaca, NY, 14853, USA.
Andrew J ModzelewskiDepartment of Molecular and Cellular Biology, University of California, Berkeley, Berkeley, CA, USA.
Tyler T MaleyDepartment of Biomedical Sciences and Center for Reproductive Genomics, Cornell University, Tower Road, Ithaca, NY, 14853, USA.
Kadeine M Campbell-PetersonDepartment of Biomedical Sciences and Center for Reproductive Genomics, Cornell University, Tower Road, Ithaca, NY, 14853, USA.
J Kim HollowayDepartment of Biomedical Sciences and Center for Reproductive Genomics, Cornell University, Tower Road, Ithaca, NY, 14853, USA.
Paula E CohenDepartment of Biomedical Sciences and Center for Reproductive Genomics, Cornell University, Tower Road, Ithaca, NY, 14853, USA. paula.cohen@cornell.edu.
Cornell University · USUniversity of California, Berkeley · US

Funding

The MLH1-MLH3 Heterodimer in Mammalian Meiotic Recombination and GameogenesisR01HD041012 · NICHD · YESHIVA UNIVERSITY · PI Paula Elaine Cohen · 2003 to 2026
$7.9M
Reproductive Sciences and Genomics Training ProgramT32HD052471 · NICHD · CORNELL UNIVERSITY · PI ROBERSON, MARK S · 2007 to 2016
$2.0M
Genetic Pathways Effecting Crossover Control and Meiotic Recombination in MammalsR01GM097263 · NIGMS · CORNELL UNIVERSITY · PI COHEN, PAULA ELAINE · 2012 to 2015
$1.1M
Functional Analysis of the Dual Specificity Kinase NEK1 in Mammalian MeiosisR00HD065870 · NICHD · CORNELL UNIVERSITY · PI HOLLOWAY, JOANNA KIM · 2012 to 2014
$1.1M
Functional Analysis of the Dual Specificity Kinase NEK1 in Mammalian MeiosisK99HD065870 · NICHD · CORNELL UNIVERSITY · PI HOLLOWAY, JOANNA KIM · 2010 to 2011
$291k
NICHD NIH HHS HD065870NICHD NIH HHS K99 HD065870NICHD NIH HHS R00 HD065870NICHD NIH HHS R01 HD041012NICHD NIH HHS T32 HD052471NIGMS NIH HHS GM097263NIGMS NIH HHS R01 GM097263
6 · The paper itself

Abstract

Fancj, the gene associated with Fanconi anemia (FA) Complementation Group J, encodes a DNA helicase involved in homologous recombination repair and the cellular response to replication stress. FANCJ functions in part through its interaction with key DNA repair proteins, including MutL homolog-1 (MLH1), Breast Cancer Associated gene-1 (BRCA1), and Bloom syndrome helicase (BLM). All three of these proteins are involved in a variety of events that ensure genome stability, including the events of DNA double strand break (DSB) repair during prophase I of meiosis. Meiotic DSBs are repaired through homologous recombination resulting in non-crossovers (NCO) or crossovers (CO). The frequency and placement of COs are stringently regulated to ensure that each chromosome receives at least one CO event, and that longer chromosomes receive at least one additional CO, thus facilitating the accurate segregation of homologous chromosomes at the first meiotic division. In the present study, we investigated the role of Fancj during prophase I using a gene trap mutant allele. Fancj (GT/GT) mutants are fertile, but their testes are very much smaller than wild-type littermates, predominantly as a result of impeded spermatogonial proliferation and mildly increased apoptosis during testis development in the fetus. This defect in spermatogonial proliferation is consistent with mutations in other FA genes. During prophase I, early events of synapsis and DSB induction/repair appear mostly normal in Fancj (GT/GT) males, and the FANCJ-interacting protein BRCA1 assembles normally on meiotic chromosome cores. However, MLH1 focus frequency is increased in Fancj (GT/GT) males, indicative of increased DSB repair via CO, and is concomitant with increased chiasmata at diakinesis. This increase in COs in the absence of FANCJ is associated with increased localization of BLM helicase protein, indicating that BLM may facilitate the increased rate of crossing over in Fancj (GT/GT) males. Taken together, these results demonstrate a critical role for FANCJ in spermatogenesis at two stages: firstly in the proliferative activity that gives rise to the full complement of testicular spermatogonia and secondly in the establishment of appropriate CO numbers during prophase I.

Indexed as

Crossing Over, GeneticMeiotic Prophase IAllelesAnimalsBasic-Leucine Zipper Transcription FactorsDNA Breaks, Double-StrandedDNA RepairFanconi Anemia Complementation Group ProteinsMaleMiceRecombination, GeneticRNA HelicasesSpermatogenesisSpermatogoniaBasic-Leucine Zipper Transcription FactorsBrip1 protein, mouseFanconi Anemia Complementation Group ProteinsRNA HelicasesBACH1BRIP1Fanconi anemiaGametogenesisMeiotic prophase IMLH1

Identifiers

PMID26490168
PMCPMC5415080
OpenAlexW1786442921

What OpenQuestion holds

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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.