Evidence map›Paper›PMID 36964127›Full record

ArticleNature communications2023

The m6A reader PRRC2A is essential for meiosis I completion during spermatogenesis.

Xinshui Tan, Caihong Zheng, Yinghua Zhuang, Pengpeng Jin, Fengchao Wang

Open access · goldFull text read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
12.6field-weighted citation impact, top 1% 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

40 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. PRRC2A-mediated mCell death & disease · 2026
    Article
  3. mJournal of assisted reproduction and genetics · 2026
    Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. IGF2BP3 recognizes mThe EMBO journal · 2026
    Article
  10. The emerging role of mFrontiers in immunology · 2026
    Review
  11. Article
  12. Review
  13. mAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  14. Therapeutic Repair of Sperm Quality Decline Caused by Polytetrafluoroethylene.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  15. Epigenetic Effects and Potential Contributions of mAnimals : an open access journal from MDPI · 2025
    Article
  16. Article
  17. Article
  18. Review
  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

5 authors at 3 institutions in 1 country.

Xinshui Tan *Graduate School of Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
Caihong Zheng *Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, and China National Center for Bioinformation, Beijing, 100101, China.
Yinghua ZhuangNational Institute of Biological Sciences, Beijing, China.
Pengpeng JinNational Institute of Biological Sciences, Beijing, China.
Fengchao WangGraduate School of Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China. wangfengchao@nibs.ac.cn.ORCID 0000-0003-4252-5406
Chinese Academy of Medical Sciences & Peking Union Medical College · CNNational Institute of Biological Sciences, Beijing · CNChinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N6-methyladenosine (m6A) and its reader proteins YTHDC1, YTHDC2, and YTHDF2 have been shown to exert essential functions during spermatogenesis. However, much remains unknown about m6A regulation mechanisms and the functions of specific readers during the meiotic cell cycle. Here, we show that the m6A reader Proline rich coiled-coil 2A (PRRC2A) is essential for male fertility. Germ cell-specific knockout of Prrc2a causes XY asynapsis and impaired meiotic sex chromosome inactivation in late-prophase spermatocytes. Moreover, PRRC2A-null spermatocytes exhibit delayed metaphase entry, chromosome misalignment, and spindle disorganization at metaphase I and are finally arrested at this stage. Sequencing data reveal that PRRC2A decreases the RNA abundance or improves the translation efficiency of targeting transcripts. Specifically, PRRC2A recognizes spermatogonia-specific transcripts and downregulates their RNA abundance to maintain the spermatocyte expression pattern during the meiosis prophase. For genes involved in meiotic cell division, PRRC2A improves the translation efficiency of their transcripts. Further, co-immunoprecipitation data show that PRRC2A interacts with several proteins regulating mRNA metabolism or translation (YBX1, YBX2, PABPC1, FXR1, and EIF4G3). Our study reveals post-transcriptional functions of PRRC2A and demonstrates its critical role in the completion of meiosis I in spermatogenesis.

Indexed as

MeiosisSpermatogenesisHumansMaleProphaseRNASex ChromosomesSpermatocytesRNA

Identifiers

PMID36964127
PMCPMC10039029
OpenAlexW4360853927

What Socratic holds

Textfull text, public
LicenceCC BY
reference markers read1
measurements read161
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 Socratic graph.