Evidence map›Paper›PMID 36938872›Full record

ArticleNucleic acids research2023

SPIDR is required for homologous recombination during mammalian meiosis.

Tao Huang, Xinyue Wu, Shiyu Wang, Ziyou Bao, Yanling Wan, Ziqi Wang, Mengjing Li, Xiaochen Yu, Yue Lv, Zhaojian Liu and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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  6. mAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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  12. Genetic insights into the complexity of premature ovarian insufficiency.Reproductive biology and endocrinology : RB&E · 2024
    Review
  13. 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

16 authors at 2 institutions in 2 countries.

Tao HuangCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.
Xinyue WuCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.
Shiyu WangCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.
Ziyou BaoCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.
Yanling WanCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.
Ziqi WangCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.
Mengjing LiCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.
Xiaochen YuCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.
Yue LvShandong Key Laboratory of Reproductive Medicine, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Zhaojian LiuAdvanced Medical Research Institute, Shandong University, Jinan, China.ORCID 0000-0002-2542-0859
Xiangfeng ChenShanghai Key Laboratory for Assisted Reproduction and Reproductive Genetics, Shanghai200135, China.
Wai-Yee ChanCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.
Fei GaoCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.ORCID 0000-0002-4029-6411
Gang LuCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.
Zi-Jiang ChenCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.ORCID 0000-0001-6637-6631
Hongbin LiuCenter for Reproductive Medicine, Shandong University, Jinan, Shandong250012, China.ORCID 0000-0003-2550-7492
Shandong University · CNChinese University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Meiotic recombinases RAD51 and DMC1 mediate strand exchange in the repair of DNA double-strand breaks (DSBs) by homologous recombination. This is a landmark event of meiosis that ensures genetic diversity in sexually reproducing organisms. However, the regulatory mechanism of DMC1/RAD51-ssDNA nucleoprotein filaments during homologous recombination in mammals has remained largely elusive. Here, we show that SPIDR (scaffold protein involved in DNA repair) regulates the assembly or stability of RAD51/DMC1 on ssDNA. Knockout of Spidr in male mice causes complete meiotic arrest, accompanied by defects in synapsis and crossover formation, which leads to male infertility. In females, loss of Spidr leads to subfertility; some Spidr-/- oocytes are able to complete meiosis. Notably, fertility is rescued partially by ablation of the DNA damage checkpoint kinase CHK2 in Spidr-/- females but not in males. Thus, our study identifies SPIDR as an essential meiotic recombination factor in homologous recombination in mammals.

Indexed as

Cell Cycle ProteinsRad51 RecombinaseAnimalsChromosome PairingDNA-Binding ProteinsDNA RepairHomologous RecombinationMaleMammalsMeiosisMiceMice, KnockoutCell Cycle ProteinsDNA-Binding ProteinsRad51 RecombinaseSpidr protein, mouse

Identifiers

PMID36938872
PMCPMC10164582
OpenAlexW4327895858

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.