Integrative Transcriptomic and Metabolomic Analysis of Muscle and Liver Reveals Key Molecular Pathways Influencing Growth Traits in Zhedong White Geese.

IF 2.7 2区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Animals Pub Date : 2025-05-06 DOI:10.3390/ani15091341
Kai Shi, Xiao Zhou, Jiuli Dai, Yuefeng Gao, Linna Gao, Yangyang Shen, Shufang Chen
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引用次数: 0

Abstract

Geese (Anser cygnoides) are popular worldwide with consumers for their unique meat quality, egg production, foie gras, and goose down; however, the key genes that influence geese growth remain elusive. To explore the mechanism of geese growth, a total of 500 Zhedong White geese were raised; four high-weight (HW) and four low-weight (LW) male geese were selected to collect carcass traits and for further transcriptomic and metabolomic analysis. The body weight and average daily gain of HW geese were significantly higher than those of the LW geese (p-value < 0.05), and the yields of the liver, gizzard, glandular stomach, and pancreas showed no significant difference between the HW and the LW group (p-value > 0.05). Compared with the LW geese, 19 differentially expressed genes (DEGs) (i.e., COL11A2, COL22A1, and TF) were detected in the breast muscle from the HW geese, which were involved in the PPAR signaling pathway, adipocytokine signaling pathway, fatty acid biosynthesis, and ferroptosis. A total of 59 differential accumulation metabolites (DAMs), which influence the pathways of glutathione metabolism and vitamin B6 metabolism, were detected in the breast muscle between the HW and LW geese. In the liver, 106 DEGs (i.e., THSD4, CREB3L3, and CNST) and 202 DAMs were found in the livers of the HW and LW groups, respectively. DEGs regulated the pathways of the TGF-beta signaling pathway, pyruvate metabolism, and adipocytokine signaling pathway; DAMs were involved in pyrimidine metabolism, nitrogen metabolism, and phenylalanine metabolism. Correlation analysis between the top DEGs and DAMs revealed that in the breast muscle, the expression levels of COL11A2 and COL22A1 were positively correlated with the content of S-(2-Hydroxy-3-buten-1-yl)glutathione. In the liver, the expression of THSD4 was positively correlated with the content of 2-Hydroxyhexadecanoic acid. In addition, one DEG (LOC106049048) and four DAMs (mogrol, brassidic acid, flabelline, and L-Leucyl-L-alanine) were shared in the breast muscle and liver. These important results contribute to improving the knowledge of goose growth and exploring the effective molecular markers that could be adopted for Zhedong White goose breeding.

肌肉和肝脏的综合转录组学和代谢组学分析揭示了影响浙江白鹅生长性状的关键分子途径。
鹅(Anser cygnoides)因其独特的肉质、产蛋、鹅肝和鹅绒而受到全球消费者的欢迎;然而,影响鹅生长的关键基因仍然难以捉摸。为探讨鹅的生长机理,饲养了500只浙江白鹅;选取4只高体重(HW)和4只低体重(LW)雄性鹅,收集胴体性状并进行转录组学和代谢组学分析。HW组鹅的体重和平均日增重显著高于LW组(p值< 0.05),肝脏、砂囊、腺胃和胰腺产量在HW组与LW组之间无显著差异(p值< 0.05)。与LW鹅相比,HW鹅胸肌中检测到19个差异表达基因(deg),分别为COL11A2、COL22A1和TF,它们参与PPAR信号通路、脂肪细胞因子信号通路、脂肪酸生物合成和铁下垂。在高肥鹅和低肥鹅的胸肌中共检测到59种影响谷胱甘肽代谢和维生素B6代谢途径的差异积累代谢物(DAMs)。在肝脏中,HW组和LW组分别检测到106个deg(即THSD4、CREB3L3和CNST)和202个dam。DEGs调节tgf - β信号通路、丙酮酸代谢通路和脂肪细胞因子信号通路;dam参与嘧啶代谢、氮代谢和苯丙氨酸代谢。结果表明,在胸肌中,COL11A2和COL22A1的表达水平与S-(2-羟基-3-丁烯-1-酰基)谷胱甘肽的含量呈正相关。在肝脏中,THSD4的表达与2-羟基十六酸的含量呈正相关。此外,1个DEG (LOC106049048)和4个dam (mogrol, brassidic acid, flabelline和L-Leucyl-L-alanine)在乳房肌肉和肝脏中共享。这些重要结果有助于提高对鹅生长发育的认识,探索有效的分子标记,为浙江白鹅育种提供依据。
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来源期刊
Animals
Animals Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
4.90
自引率
16.70%
发文量
3015
审稿时长
20.52 days
期刊介绍: Animals (ISSN 2076-2615) is an international and interdisciplinary scholarly open access journal. It publishes original research articles, reviews, communications, and short notes that are relevant to any field of study that involves animals, including zoology, ethnozoology, animal science, animal ethics and animal welfare. However, preference will be given to those articles that provide an understanding of animals within a larger context (i.e., the animals'' interactions with the outside world, including humans). There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental details and/or method of study, must be provided for research articles. Articles submitted that involve subjecting animals to unnecessary pain or suffering will not be accepted, and all articles must be submitted with the necessary ethical approval (please refer to the Ethical Guidelines for more information).
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