Evidence map›Paper›PMID 40881635›Full record

ArticleFrontiers in veterinary science2025

Genome-wide selection signal analysis reveals copy number variation associated with litter size in Guizhou Black goat.

Yanpin Zhao, Yong Han, Chao Yuan, Yang Yang, Yong Long, Wen Xiao

Abstract read
In one paragraph

Article in Frontiers in veterinary science, 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

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Current Applications and Future Prospects of High-ThroughputAnimals : an open access journal from MDPI · 2026
    Review
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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.

Yanpin ZhaoCollege of Animal Science, Guizhou University, Guiyang, China.
Yong HanInstitute of Animal Husbandry and Veterinary Sciences, Guizhou Academy of Agricultural Sciences, Guiyang, China.
Chao YuanInstitute of Animal Husbandry and Veterinary Sciences, Guizhou Academy of Agricultural Sciences, Guiyang, China.
Yang YangInstitute of Animal Husbandry and Veterinary Sciences, Guizhou Academy of Agricultural Sciences, Guiyang, China.
Yong LongCollege of Animal Science, Guizhou University, Guiyang, China.
Wen XiaoCollege of Animal Science, Guizhou University, Guiyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Copy number variation (CNV) is a common form of genomic structural variation arising from genome sequence rearrangements, which primarily involves variations in the copy number of large genomic segments. This study focuses on performing selection signal analysis of CNVs to identify candidate loci and genes associated with litter size in Guizhou Black goat. Methods: Sample selection: 30 Guizhou Black goats were divided into high-lambing and low-lambing groups based on their continuous lambing records. Genetic analysis: Phylogenetic tree construction and principal component analysis (PCA) were performed to assess genetic differences between the two groups. Selection signal indicators: Genetic differentiation index (FST) and nucleotide diversity (θπ) were used as indicators for identifying selection signals. CNV identification: 180 CNVs associated with litter size were identified through selection signal analysis. Functional annotation: Candidate genes within these CNVs were annotated, and further analysis was conducted using Gene Ontology (GO) and KEGG pathway enrichment methods. Results: Genetic differentiation: Phylogenetic tree construction and PCA revealed significant differences in genetic structure between the high-lambing and low-lambing groups. CNV identification: 180 CNVs were found to be associated with litter size. Candidate genes: Functional annotation of the CNVs identified 49 candidate genes. Pathway enrichment: GO and KEGG pathway analysis revealed significant enrichment of these genes in several reproduction-related biological pathways, including the Hippo signaling pathway, steroid hormone biosynthesis, and retinol metabolism. Discussion: This study provides novel insights into the genetic mechanisms underlying prolificacy in Guizhou Black goats. The identification of CNVs associated with litter size offers potential targets for genomic selection breeding, which could be used to improve reproductive traits in this breed. The enriched pathways, such as the Hippo signaling pathway, steroid hormone biosynthesis, and retinol metabolism, suggest that these biological processes may play a critical role in regulating fertility and reproductive efficiency in goats. The findings highlight the potential for utilizing CNVs as markers for improving reproductive performance in livestock breeding programs.

Indexed as

CNVgoatslitter sizeselect signalwhole genome sequencing

Identifiers

PMID40881635
PMCPMC12381683

What Socratic holds

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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 Socratic graph.