Evidence map›Paper›PMID 40369756›Full record

ArticleAnimal bioscience2025

Dynamic changes in chromatin accessibility and gene expression involved in fetal myogenesis of Min pigs.

Xinhua Hou, Naiqi Niu, Xin Liu, Ligang Wang, Lixian Wang, Longchao Zhang

Abstract read
In one paragraph

Article in Animal bioscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

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4 · The record

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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

6 authors.

Xinhua HouInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Naiqi NiuInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Xin LiuInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Ligang WangInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Lixian WangInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Longchao ZhangInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China.

Funding

Agricultural Science and Technology Innovation Project CAAS-ZDRW202406China Agriculture Research System of MOF and MARA
6 · The paper itself

Abstract

objectiveChinese fat-type pig breeds possess good meat quality, but their growth rate and lean meat percentage are not dominant. Investigating the dynamic transcriptional regulation of skeletal muscle development could help improve meat yield in these breeds. However, little is known about chromatin accessibility and its association with gene expression during prenatal skeletal muscle development in these pigs.

methodsATAC-seq and RNA-seq were performed to profile chromatin accessibility and transcriptome in skeletal muscle at 45, 70, and 100 days post-coitus (E45, E75, and E100) from two male and two female full-sib fetuses of Min pig.

resultsThis study demonstrated that the majority of ATAC-seq peak signals were located within 3 kb of transcription start sites. Notably, a greater number of genes associated with differential peaks were observed in the E100 vs. E45 comparison, relative to the E70 vs. E45 and E100 vs. E75 comparisons. This finding was consistent with the RNA-seq data, where the E100 vs. E45 comparison also exhibited the highest number of differentially expressed genes. Gene Ontology analysis of the RNA-seq data demonstrated that genes involved in skeletal muscle contraction, muscle fiber development, and energy metabolism were up-regulated during fetal development, while those associated with cell cycle regulation and proliferation were down-regulated. Integration of ATAC-seq and RNA-seq data identified a few differentially expressed genes associated with chromatin accessibility, with the overlapping genes primarily related to cell proliferation in the early fetal stage and metabolism in later stages.

conclusionThis study provides significant insights into the molecular mechanisms underlying fetal skeletal muscle development in Min pigs.

Indexed as

Chromatin AccessibilityFetal PeriodMyogenesisPigTranscriptome

Identifiers

PMID40369756
PMCPMC12580940

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