@article{Xu2026, 
author = {Zhongxian Xu and Tao Wang and Wei Zhu and Maosen Yang and Dong Leng and Ziyu Li and Jiaman Zhang and Pengliang Liu and Zhoulin Wu and Mengnan He and Yan Li and Hua Kui and Xue Bai and Bo Zeng and Yao Zhang and Qing Zhu and Xiaoling Zhao and Mingzhou Li and Diyan Li},
title = {3D genomic alterations during development of skeletal muscle in chicken},
year = {2026},
journal = {Journal of Integrative Agriculture (JIA)},
volume = {25},
number = {1},
pages = {207-226},
keywords = {skeletal muscle, development, gene expression, chromatin architecture},
url = {https://www.sciopen.com/article/10.1016/j.jia.2024.03.052},
doi = {10.1016/j.jia.2024.03.052},
abstract = {The development of skeletal muscle are complicated processes involving genes responsible for proper muscle morphology, contractility, cell proliferation, differentiation, interactions, migration, and death. The three-dimensional chromatin architecture of skeletal muscle development has not been studied intensively although dynamic transcriptional regulation during differentiation of muscle cells is one of the most deeply studied processes. The RNA-seq was used to analyze the transcriptome pattern during chicken muscle development across 12 stages. Hi-C was used to build chromatin architectures during four representative stages. ChIP-seq was conducted to identify enhancers and promoters in these four stages, which are occupied by histone H3K27ac and H3K4me3 peaks. Results show that large-scale genome architecture changes are mostly unidirectional, and coupled by complex on/off dynamic patterns of gene expression. Specifically, we observed 258.30 Mb of the genome undergoing A/B compartment switching. Notable alterations (316.57 Mb) of interaction frequencies within TADs were observed. Substantial aging-associated genes exhibited ascending connectivity with the compartment transition from repressive to active status during muscle development. Some muscle-related gene promoters that interacted with active enhancers during development, and some myopathy/aging-associated genes that were activated in aging muscle were founded. These results provide key insights into skeletal muscle development in vivo, and offer a valuable resource that allows in-depth functional characterization of candidate genes.}
}