Genome‐Wide Association Study Identifies Novel Loci Influencing Growth Traits in Pigs

Growth traits in pigs are governed by complex polygenic architectures, with most associated loci residing in non-coding regions that exert substantial influence on economically relevant phenotypes. However, the molecular mechanisms underlying these regulatory elements remain poorly characterized. In this study, a non-coding mutation-designated as NR2C2 recognition motif sequence variation (NRMSV), located 2083 bp upstream of the HMGA1 gene-was identified as a functional modulator of growth traits in a three-generation Eurasian hybrid pig population. NR2C2 is a nuclear receptor implicated in skeletal development and metabolic regulation, while HMGA1 is a key determinant of body size across mammalian species. In embryonic fibroblasts, where NR2C2 is abundantly expressed, the mutant NRMSV suppressed transcriptional activity, functioning as a silencer. In contrast, in bone marrow mesenchymal stem cells, characterized by low NR2C2 expression, the same allele acted as a robust transcriptional enhancer. Knockdown of NR2C2 in embryonic fibroblasts abrogated this repression and restored enhancer activity, confirming the context-dependent, bidirectional regulatory effect of NRMSV on HMGA1 expression. These findings establish the NR2C2-NRMSV-HMGA1 pathway as a novel regulatory mechanism underpinning phenotypic variation in pig growth traits, offering mechanistic insights into mammalian developmental regulation and informing targeted genomic selection for improved productivity in porcine breeding programs.

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Publication Details

Journal
Animal Genetics
Published
2026-04-01
DOI
https://doi.org/10.1002/age.70097
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

Genome‐Wide Association Study Identifies Novel Loci Influencing Growth Traits in Pigs

Mo Yuan, Xian Shi, Jianbo Li, Ya‐Ping Zhang et al.
Animal Genetics
Genomics and Chromatin Dynamics
article

Genome‐Wide Association Study Identifies Novel Loci Influencing Growth Traits in Pigs

Mo Yuan, Xian Shi, Jianbo Li, Ya‐Ping Zhang, Li‐Gang Wang, Chang‐Gai Mu, Shu‐Run Zhang, Yun Gao, Ting‐Ting Yin, Ru‐Nian Wu, Li‐Shi Xie, Xuan‐Yu Gao, Man Wang
article en

Abstract

Growth traits in pigs are governed by complex polygenic architectures, with most associated loci residing in non-coding regions that exert substantial influence on economically relevant phenotypes. However, the molecular mechanisms underlying these regulatory elements remain poorly characterized. In this study, a non-coding mutation-designated as NR2C2 recognition motif sequence variation (NRMSV), located 2083 bp upstream of the HMGA1 gene-was identified as a functional modulator of growth traits in a three-generation Eurasian hybrid pig population. NR2C2 is a nuclear receptor implicated in skeletal development and metabolic regulation, while HMGA1 is a key determinant of body size across mammalian species. In embryonic fibroblasts, where NR2C2 is abundantly expressed, the mutant NRMSV suppressed transcriptional activity, functioning as a silencer. In contrast, in bone marrow mesenchymal stem cells, characterized by low NR2C2 expression, the same allele acted as a robust transcriptional enhancer. Knockdown of NR2C2 in embryonic fibroblasts abrogated this repression and restored enhancer activity, confirming the context-dependent, bidirectional regulatory effect of NRMSV on HMGA1 expression. These findings establish the NR2C2-NRMSV-HMGA1 pathway as a novel regulatory mechanism underpinning phenotypic variation in pig growth traits, offering mechanistic insights into mammalian developmental regulation and informing targeted genomic selection for improved productivity in porcine breeding programs.

Animal GeneticsVol. 57(2)
Kunming Institute of Zoology (CN), Yunnan University (CN), Chinese Academy of Agricultural Sciences (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China
Decent work and economic growth
Openalex Percentile: Top 17%
Genomics and Chromatin Dynamics
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