Evidence map›Paper›PMID 42791710›Full record

ArticleAnimals : an open access journal from MDPI2026

Transcriptomic Dynamics and ECM Remodeling During Postnatal Testicular Maturation in the Tianzhu White Yak.

Yu Shi, Bingang Shi, Youpeng Qi, Changze Cui, Meixian Zhang, Zhihao Luo, Yuwei Ma, Jiang Hu

Abstract read
In one paragraph

Article in Animals : an open access journal from MDPI, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Yu ShiGansu Key Laboratory of Herbivorous Animal Biotechnology, College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China.ORCID 0009-0006-8146-2224
Bingang ShiGansu Key Laboratory of Herbivorous Animal Biotechnology, College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China.ORCID 0000-0003-1145-991X
Youpeng QiGansu Key Laboratory of Herbivorous Animal Biotechnology, College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China.
Changze CuiGansu Key Laboratory of Herbivorous Animal Biotechnology, College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China.ORCID 0009-0002-0268-1148
Meixian ZhangGansu Key Laboratory of Herbivorous Animal Biotechnology, College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China.
Zhihao LuoGansu Key Laboratory of Herbivorous Animal Biotechnology, College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China.ORCID 0009-0009-3300-8379
Yuwei MaGansu Key Laboratory of Herbivorous Animal Biotechnology, College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China.
Jiang HuGansu Key Laboratory of Herbivorous Animal Biotechnology, College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China.

Funding

Gansu Agricultural Research System GSARS01Gansu Agricultural University GSAU‑JSFW‑2025‑152Gansu Provincial Science and Technology Department 26CXNA051
6 · The paper itself

Abstract

The molecular mechanisms underlying testicular development in the yak remain poorly understood. In this study, RNA sequencing was performed on testicular tissues from Tianzhu white yaks at three postnatal developmental stages: 0.5 (prepubertal), 2.5 (pubertal), and 4.5 (adult) years, with six animals in each group. Differential expression analysis was integrated with weighted gene co-expression network analysis (WGCNA) to characterize transcriptomic changes associated with testicular maturation. A total of 9646 differentially expressed genes (DEGs) were identified between the 0.5- and 2.5-year groups, whereas only 126 DEGs were detected between the 2.5- and 4.5-year groups, indicating that the transition to puberty represents the most dynamic phase of transcriptional reprogramming during testicular development. Functional enrichment analysis revealed that focal adhesion and extracellular matrix-receptor interaction were the most significantly enriched Kyoto Encyclopedia of Genes and Genomes pathways, suggesting a potential role for extracellular matrix (ECM) remodeling in the establishment of the blood-testis barrier and testicular maturation. WGCNA identified seven age-associated co-expression modules. The turquoise module showed the strongest positive correlation with developmental stage and was significantly enriched for genes involved in spermatid differentiation and maturation, including

Indexed as

extracellular matrixpubertyRNA-seqspermatogenesistestistranscriptomeWGCNAyak

Identifiers

PMID42791710
PMCPMC13603577

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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.