Evidence map›Paper›PMID 26566864›Full record

ArticleCell cycle (Georgetown, Tex.)2015

CHFR is important for the survival of male premeiotic germ cells.

Lin-Yu Lu, Xiaochun Yu

Abstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
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

2 authors.

Lin-Yu Lua Key Laboratory of Reproductive Genetics; Ministry of Education and Women's Reproductive Health Laboratory of Zhejiang Province; Women's Hospital; School of Medicine; Zhejiang University ; Hangzhou , Zhejiang , China.
Xiaochun Yuc Department of Cancer Genetics and Epigenetics ; Beckman Research Institute; City of Hope ; Duarte , CA USA.

Funding

Regulation of Ionizing Radiation-Induced DNA Damage ResponseR01CA130899 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, YILUN · 2009 to 2023
$5.5M
Molecular Mechanisms of BRCA1-Dependent DNA Damage Response and TumorogenesisR01CA132755 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHEN, BINGHUI · 2008 to 2019
$3.5M
Functional analysis of BRCA1 in DNA damage response and tumor suppressionR01CA187209 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YU, XIAOCHUN · 2014 to 2018
$1.7M
Functional analysis of the TET2/OGT complex in epigenetic modificationsR01GM108647 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YU, XIAOCHUN · 2015 to 2018
$1.3M
NCI NIH HHS CA130899NCI NIH HHS CA132755NCI NIH HHS CA187209NCI NIH HHS R01 CA130899NCI NIH HHS R01 CA187209NIGMS NIH HHS GM108647NIGMS NIH HHS R01 GM108647
6 · The paper itself

Abstract

DNA damage response is required for male fertility. DNA damage repair mediates recombination between homologous chromosomes in meiotic prophase, which is essential for proper chromosome segregation during meiotic division. Interestingly, some DNA damage response proteins are also required for the survival of premeiotic germ cells, but their roles in these cells are still unclear. CHFR was recently shown to participate in DNA damage response, but it remains to be established if CHFR is required for male fertility. In this study, we characterized Chfr knockout male mice and found that around 30% of them were infertile. The onset of spermatogenesis was delayed and there was significant increase in apoptosis in premeiotic germ cells. This resulted in complete loss of germ cells in testes in 3 months and azoospermia in these mice. We further demonstrated that ATM activation was compromised in the testes of these mice. Therefore, CHFR is important for the survival of male premeiotic germ cells, which is likely through maintaining genomic stability in spermatogonial stem cells.

Indexed as

MeiosisSpermatogenesisAge FactorsAnimalsApoptosisAtaxia Telangiectasia Mutated ProteinsAzoospermiaCell SurvivalEnzyme ActivationFertilityGenetic Predisposition to DiseaseGenomic InstabilityMaleMice, Inbred C57BLMice, KnockoutPhenotypeAtaxia Telangiectasia Mutated ProteinsAtm protein, mouseCHFR protein, mousePoly-ADP-Ribose Binding ProteinsTumor Suppressor ProteinsUbiquitin-Protein LigasesATM activationDNA damage repairpremeiotic germ cells

Identifiers

PMID26566864
PMCPMC4825563

What OpenQuestion holds

Textmetadata
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.