Evidence map›Paper›PMID 37847146›Full record

ArticleeLife2023

Microhomology-mediated circular DNA formation from oligonucleosomal fragments during spermatogenesis.

Jun Hu, Zhe Zhang, Sai Xiao, Yalei Cao, Yinghong Chen, Jiaming Weng, Hui Jiang, Wei Li, Jia-Yu Chen, Chao Liu

Abstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

10 authors.

Jun Hu *State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Chemistry and Biomedicine Innovation Center (ChemBIC), Department of Andrology, Nanjing Drum Tower Hospital, Nanjing University, Nanjing, China.
Zhe Zhang *Department of Urology, Department of Reproductive Medicine Center, Peking University Third Hospital, Beijing, China.
Sai XiaoGuangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Yalei CaoDepartment of Urology, Department of Reproductive Medicine Center, Peking University Third Hospital, Beijing, China.
Yinghong ChenGuangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Jiaming WengDepartment of Urology, Department of Reproductive Medicine Center, Peking University Third Hospital, Beijing, China.
Hui JiangDepartment of Urology, Department of Reproductive Medicine Center, Peking University Third Hospital, Beijing, China.
Wei LiGuangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Jia-Yu ChenState Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Chemistry and Biomedicine Innovation Center (ChemBIC), Department of Andrology, Nanjing Drum Tower Hospital, Nanjing University, Nanjing, China.ORCID 0000-0001-9449-9321
Chao LiuGuangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The landscape of extrachromosomal circular DNA (eccDNA) during mammalian spermatogenesis, as well as the biogenesis mechanism, remains to be explored. Here, we revealed widespread eccDNA formation in human sperms and mouse spermatogenesis. We noted that germline eccDNAs are derived from oligonucleosomal DNA fragmentation in cells likely undergoing cell death, providing a potential new way for quality assessment of human sperms. Interestingly, small-sized eccDNAs are associated with euchromatin, while large-sized ones are preferentially generated from heterochromatin. By comparing sperm eccDNAs with meiotic recombination hotspots and structural variations, we found that they are barely associated with de novo germline deletions. We further developed a bioinformatics pipeline to achieve nucleotide-resolution eccDNA detection even with the presence of microhomologous sequences that interfere with precise breakpoint identification. Empowered by our method, we provided strong evidence to show that microhomology-mediated end joining is the major eccDNA biogenesis mechanism. Together, our results shed light on eccDNA biogenesis mechanism in mammalian germline cells.

Indexed as

DNA, CircularSemenAnimalsChromosomesHumansMaleMammalsMiceSpermatogenesisDNA, Circulardevelopmental biologyextrachromosomal circular DNAgeneticsgenomicshumanmicrohomologymousespermatogenesis

Identifiers

PMID37847146
PMCPMC10581685

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Registered trials

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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.