Evidence map›Paper›PMID 40804371›Full record

ArticleBMC genomics2025

Single-cell RNA sequencing uncovers dynamic roadmap during chicken spermatogenesis.

Haishan Guo, Jianing Liu, Mingzhen Xu, Tingqi Zhu, Shuangxing Liu, Pingquan Liu, Huayuan Liu, Shi Tang, Zhunan Li, Weiwei Jin and 4 more

Abstract read
In one paragraph

Article in BMC genomics, 2025. 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.

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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

14 authors.

Haishan Guo *The Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China.
Jianing Liu *The Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China.
Mingzhen XuThe Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China.
Tingqi ZhuThe Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China.
Shuangxing LiuThe Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China.
Pingquan LiuThe Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China.
Huayuan LiuThe Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China.
Shi TangKey Laboratory of Livestock and Poultry Resources (Poultry) Evaluation and Utilization of Ministry of Agriculture and Rural Affairs, Henan Agricultural University, Zhengzhou, 450046, China.
Zhunan LiThe Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China.
Weiwei JinThe Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China.
Donghua LiThe Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China.
Yadong TianThe Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China.
Xiangtao KangThe Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China.
Guirong SunThe Shennong Laboratory, Henan Agricultural University, Zhengzhou, 450046, China. grsun2000@126.com.

Funding

the Science and Technology Innovation 2030 Major Projects 2023ZD0405203the Scientific Studio of Zhongyuan Scholars 234400510023This work supported by the Key Research Project of the Shennong Laboratory SN01-2022-05
6 · The paper itself

Abstract

backgroundSpermatogenesis is a pivotal biological process for the precise transmission of paternal genetic information, governed by a highly complex and dynamically regulated testicular microenvironment. Although mammalian research has characterized germ cell development at the single-cell level, differences in reproductive strategies limit the relevance of these findings to avian species.

resultsWe employed single-cell RNA sequencing (scRNA-seq) to analyze the testes of the "Yufen 1" H line roosters at five distinct developmental stages: birth, rapid testicular development, sexual maturity, physical maturity, and senescence. By constructing a single-cell transcriptomic atlas, we identified ten somatic cell subtypes and four germ cell subtypes, thereby elucidating the dynamic changes in gene expression during spermatogenesis. Notably, our findings indicate that meiosis initiates relatively early in chickens, with the formation of the blood-testis barrier being closely associated with pachytene spermatocytes. Additionally, the testicular microenvironment undergoes age-related adaptive changes. Furthermore, we observed that support cells at 20 and 80 weeks of age exhibit similar transcriptional profiles, while macrophages and T cells play a pivotal role in the formation of the testicular cords and vascular networks during the early developmental stages.

conclusionThis study offers a comprehensive atlas of testicular development in chickens, elucidating the sequential cell fate transitions from spermatogonial stem cells to mature sperm, alongside the dynamic and intricate developmental trajectories of somatic cells within the testicular microenvironment. These findings present novel insights into avian testicular development and establish a theoretical foundation for future research in reproductive biology and breeding strategies.

Indexed as

ChickensSequence Analysis, RNASingle-Cell AnalysisSpermatogenesisAnimalsGene Expression ProfilingMaleRNA-SeqTestisTranscriptomeChickenSingle cell transcriptomeSpermatogenesisTestis

Identifiers

PMID40804371
PMCPMC12351910

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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.