LEP Gene Promotes Milk Fat Synthesis via the JAK2-STAT3 and mTOR Signaling Pathways in Buffalo Mammary Epithelial Cells

被引:0
作者
Gao, Ruixia [1 ]
Zhu, Qunyao [1 ]
Huang, Lige [1 ]
Fan, Xinyang [1 ]
Teng, Xiaohong [1 ]
Miao, Yongwang [1 ]
机构
[1] Yunnan Agr Univ, Inst Anim Genet & Breeding, Coll Anim Sci & Technol, Kunming 650201, Peoples R China
来源
ANIMALS | 2024年 / 14卷 / 16期
基金
美国国家科学基金会;
关键词
buffalo LEP gene; transcript variants; gene function; milk fat synthesis; population genetic analysis; EXPRESSION; PROTEIN; TISSUE; ASSOCIATION; ACTIVATION; RECEPTOR; ADIPOSE; TRAITS;
D O I
10.3390/ani14162446
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Leptin (LEP), a protein hormone well-known for its role in metabolic regulation, has recently been linked to lipid metabolism in cattle. However, its function in buffalo mammary glands remains unclear. To address this issue, we isolated and identified the LEP gene and conducted experiments to investigate its function in buffalo mammary epithelial cells (BuMECs). In this study, two transcript variants of LEP, designated as LEP_X1 and LEP_X2, were identified. The coding sequences (CDS) of LEP_X1 and LEP_X2 are 504 bp and 579 bp in length, encoding 167 and 192 amino acid residues, respectively. Bioinformatics analysis revealed that LEP_X2 is a hydrophobic protein with an isoelectric point below 7 and contains a signal peptide, while LEP_X1 is hydrophilic and lacks a signal peptide. Our study found that LEP gene expression in lactating BuMECs was significantly higher than in non-lactating cells, with LEP_X2 expression remarkably higher than LEP_X1 in lactating BuMECs. Overexpression of both LEP_X1 and LEP_X2 significantly promoted the expression of genes related to milk fat synthesis in lactating BuMECs, including STAT3, PI3K, mTOR, SCD, and SREBF1, accompanied by an increase in cellular triglycerides (TG). Interestingly, LEP_X2 overexpression significantly suppressed LEP_X1 expression while increasing intracellular TG concentration by 12.10-fold compared to LEP_X1 overexpression, suggesting an antagonistic relationship between the two variants and supposing LEP_X2 plays a dominant role in milk fat synthesis in lactating BuMECs. Additionally, four nucleotide substitutions were identified in the buffalo LEP CDS, including a nonsynonymous substitution c.148C>T (p.Arg50Cys), which was predicted to decrease the stability of the LEP protein without affecting its function. These results collectively underscore the significant role of LEP in milk fat synthesis and can provide a basis for molecular breeding strategies of buffalo.
引用
收藏
页数:19
相关论文
共 59 条
  • [1] Leptin
    Ahima, RS
    Flier, JS
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, 2000, 62 : 413 - 437
  • [2] Ahmad S, 2013, J ANIM PLANT SCI, V23, P62
  • [3] The MEME Suite
    Bailey, Timothy L.
    Johnson, James
    Grant, Charles E.
    Noble, William S.
    [J]. NUCLEIC ACIDS RESEARCH, 2015, 43 (W1) : W39 - W49
  • [4] Bartek Josef, 2001, Biomedical Papers (Olomouc), V145, P15
  • [5] Expression of leptin and its receptors in various tissues of ruminants
    Bartha, T
    Sayed-Ahmed, A
    Rudas, P
    [J]. DOMESTIC ANIMAL ENDOCRINOLOGY, 2005, 29 (01) : 193 - 202
  • [6] SWISS-MODEL: modelling protein tertiary and quaternary structure using evolutionary information
    Biasini, Marco
    Bienert, Stefan
    Waterhouse, Andrew
    Arnold, Konstantin
    Studer, Gabriel
    Schmidt, Tobias
    Kiefer, Florian
    Cassarino, Tiziano Gallo
    Bertoni, Martino
    Bordoli, Lorenza
    Schwede, Torsten
    [J]. NUCLEIC ACIDS RESEARCH, 2014, 42 (W1) : W252 - W258
  • [7] Bonnet M, 2002, J ANIM SCI, V80, P723
  • [8] Hot topic:: An association between a leptin single nucleotide polymorphism and milk and protein yield
    Buchanan, FC
    Van Kessel, AG
    Waldner, C
    Christensen, DA
    Laarveld, B
    Schmutz, SM
    [J]. JOURNAL OF DAIRY SCIENCE, 2003, 86 (10) : 3164 - 3166
  • [9] Burland T G, 2000, Methods Mol Biol, V132, P71
  • [10] The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments
    Bustin, Stephen A.
    Benes, Vladimir
    Garson, Jeremy A.
    Hellemans, Jan
    Huggett, Jim
    Kubista, Mikael
    Mueller, Reinhold
    Nolan, Tania
    Pfaffl, Michael W.
    Shipley, Gregory L.
    Vandesompele, Jo
    Wittwer, Carl T.
    [J]. CLINICAL CHEMISTRY, 2009, 55 (04) : 611 - 622