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转录组分析揭示了不同年龄的雄性和雌性黑番鸭肌纤维发育的调控机制。

Transcriptome analysis reveals the regulatory mechanism of myofiber development in male and female black Muscovy duck at different ages.

作者信息

Zhang Weihong, Zou Mengyun, Xiong Xiaolan, Wei Yue, Ke Changling, Li Haiqin, Xie Jinfang, Wei Qipeng, Huang Jiangnan

机构信息

Institute of Animal Husbandry and Veterinary Medicine, Jiangxi Academy of Agricultural Sciences, Jiangxi Poultry Engineering Technology Research Center, Jiangxi Poultry Breeding Engineering Laboratory, Nanchang, Jiangxi, China.

Jiujiang Academy of Agricultural Sciences, Jiujiang, Jiangxi, China.

出版信息

Front Vet Sci. 2024 Nov 20;11:1484102. doi: 10.3389/fvets.2024.1484102. eCollection 2024.

DOI:10.3389/fvets.2024.1484102
PMID:39634756
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11614779/
Abstract

INTRODUCTION

Sexual dimorphism in Muscovy ducks results in substantial differences in muscle development potential between males and females, leading to significant variations in growth rates and body weights throughout their development.

METHODS

This study aimed to investigate the regulatory mechanisms underlying the differences in muscle development between genders in black Muscovy ducks, we analyzed the phenotypic characteristics and transcriptome profiles of breast muscles in male and female black Muscovy ducks at different developmental stages (postnatal days 28, 42, and 70).

RESULTS

In the analysis of tissue physical morphology, the results showed that females exhibit larger myofiber diameters and lower myofiber densities compared to males at postnatal day 42 ( < 0.05). The difference becomes more pronounced by day 70, however, no significant difference was observed at postnatal day 28. Transcriptome analysis identified a total of 1,118 unique differentially expressed genes (DEGs) across the various comparison groups. In different growth and development stages of black Muscovy ducks, the DEGs like , , , were significantly associated with myofiber hypertrophy, and key pathways such as AMPK signaling pathway, focal adhesion, and ECM-receptor interactions have been found to be closely associated with muscle size and hypertrophy. In the breast muscles of different sexes black Muscovy ducks, the DEGs such as , , , , and may be the reason for the difference in breast muscle size between male and female ducks. Furthermore, key pathways, including the cGMP-PKG signaling pathway, calcium signaling pathway, and hypertrophic cardiomyopathy are also involved in regulating the developmental potential differences in muscle between male and female ducks.

DISCUSSION

This study reveals the molecular mechanism regulating the muscle development in male and female black Muscovy ducks at different growth stages, and provides valuable insights into the specific genes responsible for muscle development, laying a theoretical foundation for enhancing the genetic quality of duck meat.

摘要

引言

番鸭的性别二态性导致雄性和雌性之间的肌肉发育潜力存在显著差异,从而在其整个发育过程中导致生长速率和体重出现显著变化。

方法

本研究旨在探究黑番鸭性别间肌肉发育差异的调控机制,我们分析了不同发育阶段(出生后第28天、42天和70天)雄性和雌性黑番鸭胸肌的表型特征和转录组图谱。

结果

在组织物理形态分析中,结果显示在出生后第42天,雌性的肌纤维直径比雄性大,肌纤维密度比雄性低(<0.05)。到第70天,这种差异更加明显,然而,在出生后第28天未观察到显著差异。转录组分析在各个比较组中总共鉴定出1118个独特的差异表达基因(DEG)。在黑番鸭不同的生长发育阶段,如 、 、 、 等差异表达基因与肌纤维肥大显著相关,并且发现关键通路如AMPK信号通路、粘着斑和细胞外基质-受体相互作用与肌肉大小和肥大密切相关。在不同性别的黑番鸭胸肌中,如 、 、 、 、 等差异表达基因可能是雌雄鸭胸肌大小差异的原因。此外,关键通路,包括cGMP-PKG信号通路、钙信号通路和肥厚型心肌病也参与调节雌雄鸭之间肌肉发育潜力的差异。

讨论

本研究揭示了不同生长阶段雄性和雌性黑番鸭肌肉发育的分子调控机制,并为负责肌肉发育的特定基因提供了有价值的见解,为提高鸭肉的遗传品质奠定了理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/6c51fe5d1ac6/fvets-11-1484102-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/8922256cd523/fvets-11-1484102-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/cbc0373d464c/fvets-11-1484102-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/667a0e383a52/fvets-11-1484102-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/df0550810495/fvets-11-1484102-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/8440790200ee/fvets-11-1484102-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/271a284eb8ae/fvets-11-1484102-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/6c51fe5d1ac6/fvets-11-1484102-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/8922256cd523/fvets-11-1484102-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/cbc0373d464c/fvets-11-1484102-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/667a0e383a52/fvets-11-1484102-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/df0550810495/fvets-11-1484102-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/8440790200ee/fvets-11-1484102-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/271a284eb8ae/fvets-11-1484102-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e015/11614779/6c51fe5d1ac6/fvets-11-1484102-g007.jpg

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