AMB_2025v15n2

Animal Molecular Breeding, 2025, Vol.15, No.2, 60-71 http://animalscipublisher.com/index.php/amb 70 growth and development, and identify key regulatory factors. Interaction between transgenerational genetics and epigenetics: Study the cumulative effect of epigenetic variation in poultry breeding selection, explore whether certain epigenetic markers can serve as auxiliary breeding indicators, and how epigenetic interacts with gene mutations to influence traits. Environmental-Epigenetic Interaction Research: Systematically evaluate the changes in epigenetic markers of ducks under different environmental conditions, find beneficial variants and try to solidify these variants to improve breeds. To achieve the above goals, scientific research institutions, breeding enterprises and breeding units should strengthen cooperation. At the basic research level, a duck epigenetic research alliance can be established to share duck genomic resources and epigenetic data, strengthen communication with researchers of model species such as chickens, and learn from research experience. At the application level, industrial experimental cooperation can be carried out, such as the company provides experimental scenarios for different feeding conditions, and scientific researchers conduct biological sample collection and epigenetic analysis to screen out best practice plans. Only through the combination of industry, academia and research can laboratory discoveries be converted into productivity in the farm faster. Acknowledgements The authors gratefully acknowledge the support provided by Cai R.X. and thank the two peer reviewers for their suggestions. Conflict of Interest Disclosure The authors confirm that the study was conducted without any commercial or financial relationships and could be interpreted as a potential conflict of interest. References Bodin L., Secula A., Chapuis H., Cornuez A., Lessire M., Cobo E., Marie-Louise S., Bonnefont C., Barrieu J., Mercerand F., Bravo C., Manse H., Bourhis M., Martin X., Pitel F., Brun J., and Morisson M., 2019, Dietary methionine deficiency reduces laying performances of female common ducks and impacts traits of interest of their mule ducklings, Poultry Science, 98(9): 4035-4045. https://doi.org/10.3382/ps/pez315 Chen C., Chang Y., Jiang T., Yue Z., Liu T., Lu J., Yu Z., Lin J., Vu T., Huang T., Harn H., Ng C., Wu P., Chuong C., and Li W., 2024, Conserved regulatory switches for the transition from natal down to juvenile feather in birds, Nature Communications, 15: 48303. https://doi.org/10.1038/s41467-024-48303-3 Chen X., Ge K., Wang M., Zhang C., and Geng Z., 2017, Integrative analysis of the Pekin duck (Anas anas) microRNAome during feather follicle development, BMC Developmental Biology, 17(1): 12. https://doi.org/10.1186/s12861-017-0153-1 Chen J., and Li X., 2024, Delayed plumage maturation in juvenile males of the white-bellied shortwing (Brachypteryx leucophrys), International Journal of Molecular Zoology, 14(3): 141-153. Cong W., Han W., Liu J., Zhu J., Liu X., and Yang M., 2023, Embryonic thermal manipulation leads growth inhibition and reduced hepatic insulin-like growth factor1 expression due to promoter DNA hypermethylation in broilers, Poultry Science, 102(4): 102562. Dunislawska A., Pietrzak E., Sławińska A., Siwek M., and Bednarczyk M., 2022, Pre-hatching and post-hatching environmental factors related to epigenetic mechanisms in poultry, Animals, 12(3): 332. https://doi.org/10.3390/ani12030332 Gajendran K., and Veeramani P., 2022, Intensive Duck Rearing, in Duck Production and Management Strategies, Springer. https://doi.org/10.1007/978-981-16-6100-6_7 Gu L., Zhang S., Li B., Jiang Q., Xu T., Huang Y., Lin D., Xing M., Huang L., Zheng X., Wang F., Chao Z., and Sun W., 2022, m6A and miRNA jointly regulate the development of breast muscles in duck embryonic stages, Frontiers in Veterinary Science, 9: 933850. https://doi.org/10.3389/fvets.2022.933850 Huang Z., Hu L., Liu Z., Jin J., Xu Z., Zuo B., and Zhu Q., 2025, The functions and regulatory mechanisms of histone modifications in skeletal muscle development and disease, International Journal of Molecular Sciences, 26(8): 3644. https://doi.org/10.3390/ijms26083644 Ji G., Zhang M., Tu Y., Liu Y., Shan Y., Ju X., Zou J., Shu J., Sheng Z., and Li H., 2023, Molecular regulatory mechanisms in chicken feather follicle morphogenesis, Genes, 14(8): 1646. https://doi.org/10.3390/genes14081646 Li R., Li D., Xu S., Zhang P., Zhang Z., He F., Li W., Sun G., Jiang R., Li Z., Tian Y., Liu X., and Kang X., 2024, Whole-transcriptome sequencing reveals a melanin-related ceRNA regulatory network in the breast muscle of Xichuan black-bone chicken, Poultry Science, 103: 103539. https://doi.org/10.1016/j.psj.2024.103539 Lu J., Yu Z., Lin J., Chang Y.M., Jiang T.X., Yue Z., Liu T.Y., Vu T.D., Huang T.Y., Harn H.I., Ng C.S., Wu P., Chuong C.M., and Li W.H., 2024, Conserved regulatory switches for the transition from natal down to juvenile feather in birds, Nature Communications, 15: 4174. https://doi.org/10.1038/s41467-024-48303-3

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