Official Journal of the College of Veterinary Medicine, University of Al-Qadisiyah
Investigation of the relationship between Myoz1 gene expression, glycogen levels, and age in the iliofibularis muscle of broiler chickens (Gallus gallus domesticus)
This study aimed to investigate the histological growth and Myoz1 gene expression and evaluated the level of glycogen in the iliofibularis muscle of broiler chickens at 2, 4, and 5 weeks of age. By investigating the structural changes in muscle fibers and the corresponding alterations in Myoz1 gene levels, this research sought to elucidate the relationship between age, muscle growth, and gene expression in the iliofibularis muscle group. Understanding these developmental processes is crucial for optimizing broiler production and potentially providing insights into muscle growth and development in other species. In this study, fifteen broiler chickens were examined to investigate the histological structure and evaluate the level of the Myoz1 gene in the iliofibularis muscles at three different ages: 2 weeks, 4 weeks, and 5 weeks. The muscle fibers are cylindrical and multinucleated, with elongated nuclei beneath the sarcolemma. The muscle fibers are surrounded by a very thin layer of endomysium, which is composed of fibroelastic connective tissue. Each fascicle of muscle fibers is surrounded by a dense, irregular connective tissue called the perimysium. A cluster of muscle fascicles is surrounded by a layer of dense, irregular connective tissue called the epimysium. The size and organization of muscle fibers increase with age. At 5 weeks, the muscle fibers become larger and more uniform. The mean areas of muscle fibers at 2 weeks, 4 weeks, and 5 weeks were 233.1± 0.0099, 492.32± 0.0079, and 1177.56± 0.0098 µm2, respectively. Our results show the muscle fibers in the third group had a highly significant difference from the muscle fibers of the iliofibularis muscle in the first and second groups. The highest average expression was found in the third group (5 weeks old), while the lowest was in the first group (2 weeks old). Our findings indicate statistical analysis confirmed iliofibularis muscle in the third group had a highly significant difference with iliofibularis muscle in the first and second groups (Ƿ=0.0000269) and (Ƿ=0.000025), respectively. Overall, the findings suggested an age-dependent rise in myzo1 gene expression within the iliofibularis muscle in the third group of broiler chickens.
Bessei W. Welfare of broilers: a review. World's Poultry Sci J. 2006;62(3):455-466.https://doi.org/10.1079/WPS2005108
Alagawany M, Elnesr SS, Farag MR, Tiwari R, Yatoo MI, Karthik K, Michalak I, Dhama K. Nutritional significance of amino acids, vitamins and minerals as nutraceuticals in poultry production and health: A comprehensive review. Vet Q. 2020;41(1):1-29.https://doi.org/10.1080/01652176.2020.1857887
Kanakachari M, Bhattacharya TK. Transcriptome analysis reveals potential mechanisms and pathways underlying embryonic development with respect to muscle growth and egg production in slow and fast-growing chickens.
Bombik E, Pietrzkiewicz K, Bombik A. Analysis of the fatty acid profile of the tissues of hunted mallard ducks (Anas platyrhynchos L.) from Poland. Animals. 2022;12(18).https://doi.org/10.3390/ani12182394
Aw-Hassan A, Shomo F, Iniguez L. Trends in small ruminant meat production-consumption gaps in West Asia and North Africa: Implications for intra-regional trade. Outlook Agric. 2010;39(1).https://doi.org/10.5367/000000010791170031
Fatchiyah F, Rohmah RN, Triprisila LF, Virgirinia RP, Rahayudi B, Kurnianingsih N, Safitri A, Abdul Razis AF. The expression of Myoz1 and ApoB is positively correlated with meat quality of broiler chicken. Vet Med Int. 2022.https://doi.org/10.1155/2022/3266076
Zhou T, Wu Y, Bi Y, Bai H, Jiang Y, Chen G, Chang G, Wang Z. MYOZ1 gene promotes muscle growth and development in meat ducks. Genes. 2022;13(9).https://doi.org/10.3390/genes13091574
Suman SP, Joseph P. Myoglobin chemistry and meat color. Annu Rev Food Sci Technol. 2013;4(1):79-99.https://doi.org/10.1146/annurev-food-030212-182623
Henchion M, McCarthy M, Resconi VC, Troy D. Meat consumption: Trends and quality matters. Meat Sci. 2014;98(3):561-568. https://doi.org/10.1016/j.meatsci.2014.06.007
Suvarna SK, Layton C, Bancroft JD. Bancroft's theory and practice of histological techniques. Nottingham, UK: Elsevier; 2013.
Kong BW, Hudson N, Seo D, Lee S, Khatri B, Lassiter K, Cook D, Piekarski A, Dridi S, Anthony N, Bottje W. RNA sequencing for global gene expression associated with muscle growth in a single male modern broiler line compared to a foundational Barred Plymouth Rock chicken line. BMC Genomics. 2017;18(1). https://doi.org/10.1186/s12864-016-3471-y
Atabo D. Gross and histological studies of muscles of flight in some avian species. Arch Anim Poultry Sci. 2020;1(4). https://doi.org/10.19080/AAPS.2020.01.555566
Endo H, Tsunekaw N, Kudo K, Oshida T, Motokawa M, Sonoe M, Wanghongsa S, Tirawattanawanich C, Phimphachanhvongsod V, Takeshi S, Takahiro Y, Akishinonomiya F. Comparative morphological study of skeletal muscle weight among the red jungle fowl (Gallus gallus) and various fowl breeds (Gallus domesticus). J Exp Zool B Mol Dev Evol. 2021;338:542-555. https://doi.org/10.1002/jez.b.23111
Achouri A, Melizi M, Belbedj H, Azizi A. Comparative study of histological and histo-chemical image processing in muscle fiber section of broiler chicken. J Appl Poultry Res. 2021;30(3). https://doi.org/10.1016/j.japr.2021.100173
Telley IA, Denoth J, Stüssi E, Pfitzer G, Stehle R. Half-sarcomere dynamics in myofibrils during activation and relaxation studied by tracking fluorescent markers. Biophys J. 2006;90(2):514-530. https://doi.org/10.1529/biophysj.105.070334
Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2 C T method. Methods. 2001;2(5):402-408. https://doi.org/10.1006/meth.2001.1262
Mazzoni M, Petracci M, Meluzzi A, Cavani C, Clavenzani P, Sirri F. Relationship between pectoralis major histology and quality traits of chicken meat. Poult Sci. 2015;94(1):123-130. https://doi.org/10.3382/ps/peu043
Mellor DB. The influence of glycogen on meat tenderness. Texas Agric Exp Station, College Station, Texas. 1985;1:1028-1034. https://doi.org/10.3382/ps.0371028
Ren RM, Liu H, Zhao SH, Cao JH. Targeting of miR-432 to Myozenin1 to regulate myoblast proliferation and differentiation. Genet Mol Res. 2016;15. https://doi.org/10.4238/gmr15049313
Baqer,A Abdulshahid and Almamoori,N Abd. (2025). Investigation of the relationship between Myoz1 gene expression, glycogen levels, and age in the iliofibularis muscle of broiler chickens (Gallus gallus domesticus). Al-Qadisiyah Journal of Veterinary Medicine Sciences, 24(1), 7-13. doi: 10.29079/qjvms.2024.150688.1018
MLA
Baqer,A Abdulshahid, and Almamoori,N Abd. "Investigation of the relationship between Myoz1 gene expression, glycogen levels, and age in the iliofibularis muscle of broiler chickens (Gallus gallus domesticus)", Al-Qadisiyah Journal of Veterinary Medicine Sciences, 24, 1, 2025, 7-13. doi: 10.29079/qjvms.2024.150688.1018
HARVARD
Baqer A Abdulshahid, Almamoori N Abd. (2025). 'Investigation of the relationship between Myoz1 gene expression, glycogen levels, and age in the iliofibularis muscle of broiler chickens (Gallus gallus domesticus)', Al-Qadisiyah Journal of Veterinary Medicine Sciences, 24(1), pp. 7-13. doi: 10.29079/qjvms.2024.150688.1018
CHICAGO
A Abdulshahid Baqer and N Abd Almamoori, "Investigation of the relationship between Myoz1 gene expression, glycogen levels, and age in the iliofibularis muscle of broiler chickens (Gallus gallus domesticus)," Al-Qadisiyah Journal of Veterinary Medicine Sciences, 24 1 (2025): 7-13, doi: 10.29079/qjvms.2024.150688.1018
VANCOUVER
Baqer A Abdulshahid, Almamoori N Abd. Investigation of the relationship between Myoz1 gene expression, glycogen levels, and age in the iliofibularis muscle of broiler chickens (Gallus gallus domesticus). QJVMS. 2025;24(1):7-13. doi: 10.29079/qjvms.2024.150688.1018