본문 바로가기
KERD
논문KCI 등재

Bta-miR-365-3p-targeted FK506-binding protein 5 participates in the AMPK/mTOR signaling pathway in the regulation of preadipocyte differentiation in cattle

2

조회

0

다운로드

0

인용

0

참고문헌

키워드

초록

Objective: MicroRNAs (miRNAs) are endogenous non-coding RNAs that can play a role in the post-transcriptional regulation of mammalian preadipocyte differentiation. However, the precise functional mechanism of its regulation of fat metabolism is not fully understood.Methods: We identified bta-miR-365-3p, which specifically targets the 3′ untranslated region (3′UTR) of the FK506-binding protein 5 (FKBP5), and verified its mechanisms for regulating expression and involvement in adipogenesis.Results: In this study, we found that the overexpression of bta-miR-365-3p significantly decreased the lipid accumulation and triglyceride content in the adipocytes. Compared to inhibiting bta-miR-36 5-3p group, overexpression of bta-miR-365-3p can inhibit the expression of adipocyte differentiation-related genes <i>C/EBPα</i> and <i>PPARγ</i>. The dualluciferase reporter system further validated the targeting relationship between bta-miR-365-3p and FKBP5. FKBP5 mRNA and protein expression were detected by quantitative real-time polymerase chain reaction and Western blot. Overexpression of bta-miR-365-3p significantly down-regulated FKBP5 expression, while inhibition of bta-miR-365-3p showed the opposite, indicating that bta-miR-365-3p negatively regulates FKBP5. Adenosine 5′-monophosphate (AMP)-activated protein kinase/mammalian target of rapamycin (AMPK/mTOR) signaling pathway is closely related to the regulation of cell growth and is involved in the development of bovine adipocytes. In this study, overexpression of bta-miR-365-3p significantly inhibited mRNA and protein expression of <i>AMPK, mTOR</i>, and <i>SREBP1</i> genes, while the inhibition of bta-miR-365-3p expression was contrary to these results. Overexpression of FKBP5 significantly upregulated <i>AMPK, mTOR</i>, and <i>SREBP1</i> gene expression, while inhibition of FKBP5 expression was contrary to the above experimental results.Conclusion: In conclusion, these results indicate that bta-miR-365-3p may be involved in the AMPK/mTOR signaling pathway in regulating Yanbian yellow cattle preadipocytes differentiation by targeting the <i>FKBP5</i> gene.

Abstract

Objective: MicroRNAs (miRNAs) are endogenous non-coding RNAs that can play a role in the post-transcriptional regulation of mammalian preadipocyte differentiation. However, the precise functional mechanism of its regulation of fat metabolism is not fully understood. Methods: We identified bta-miR-365-3p, which specifically targets the 3′ untranslated region (3′UTR) of the FK506-binding protein 5 (FKBP5), and verified its mechanisms for regulating expression and involvement in adipogenesis. Results: In this study, we found that the overexpression of bta-miR-365-3p significantly decreased the lipid accumulation and triglyceride content in the adipocytes. Compared to inhibiting bta-miR-36 5-3p group, overexpression of bta-miR-365-3p can inhibit the expression of adipocyte differentiation-related genes C/EBPα and PPARγ. The dualluciferase reporter system further validated the targeting relationship between bta-miR365-3p and FKBP5. FKBP5 mRNA and protein expression were detected by quantitative real-time polymerase chain reaction and Western blot. Overexpression of bta-miR-365- 3p significantly down-regulated FKBP5 expression, while inhibition of bta-miR-365-3p showed the opposite, indicating that bta-miR-365-3p negatively regulates FKBP5. Adenosine 5′-monophosphate (AMP)-activated protein kinase/mammalian target of rapamycin (AMPK/ mTOR) signaling pathway is closely related to the regulation of cell growth and is involved in the development of bovine adipocytes. In this study, overexpression of bta-miR-365- 3p significantly inhibited mRNA and protein expression of AMPK, mTOR, and SREBP1 genes, while the inhibition of bta-miR-365-3p expression was contrary to these results. Overexpression of FKBP5 significantly upregulated AMPK, mTOR, and SREBP1 gene expression, while inhibition of FKBP5 expression was contrary to the above experimental results. Conclusion: In conclusion, these results indicate that bta-miR-365-3p may be involved in the AMPK/mTOR signaling pathway in regulating Yanbian yellow cattle preadipocytes differentiation by targeting the FKBP5 gene.

참고문헌 (30)

  1. Hoehne A, "Relationships between intramuscular fat content, selected carcass traits, and fatty acid profile in bulls using a F2-population", Meat Sci, 90, pp.629~635 (2012)[DOI]
  2. Stewart SM, "Prediction of consumer palatability in beef using visual marbling scores and chemical intramuscular fat percentage", Meat Sci, 181, pp.108322~ (2020)[DOI]
  3. Baik M, "Triennial growth and development symposium : molecular mechanisms related to bovine intramuscular fat deposition in the longissimus muscle", J Anim Sci, 95, pp.2284~2303 (2017)[DOI]
  4. Yan CG, "Study on the beef quality traits of Yanbian cattle", J Yellow Cattle Sci, 30, pp.5~7 (2004)
  5. Dani C, "Differentiation of embryonic stem cells into adipocytes in vitro", J Cell Sci, 110, pp.1279~1285 (1997)[DOI]
  6. Ali AT, "Adipocyte and adipogenesis", Eur J Cell Biol, 92, pp.229~236 (2013)[DOI]
  7. Mota de Sá P, "Transcriptional regulation of adipogenesis", Compr Physiol, 7, pp.635~674 (2017)[DOI]
  8. Wu Z, "Cross-regulation of C", EBP alpha and PPAR gamma controls the transcriptional pathway of adipogenesis and insulin sensitivity, 1999, pp.3, 151~158
  9. Liu KS, "Research progress in molecular biology related quantitative methods of MicroRNA", Am J Transl Res, 12, pp.3198~3211 (2020)
  10. Olena AF, "Genomic organization of microRNAs", J Cell Physiol, 222, pp.540~545 (2010)[DOI]
  11. Esau C, "MicroRNA-143 regulates adipocyte differentiation", J Biol Chem, 279, pp.52361~52365 (2004)[DOI]
  12. Xu H, "miR-381Targets KCTD15 to regulate bovine preadipocyte differentiation in vitro", Horm Metab Res, 53, pp.63~70 (2021)[DOI]
  13. Ma XY, "Bta-miR-130a", b regulates preadipocyte differentiation by targeting PPARG and CYP2U1in beef cattle, 2018, pp.42, 10~17
  14. Chen L, "MiR-540 as a novel adipogenic inhibitor impairs adipogenesis via suppression of PPARγ", J Cell Biochem, 116, pp.969~976 (2015)[DOI]
  15. Xia GJ, "Screening of candidate genes associated to meat quality traits of Yanbian yellow cattle by a combination of miRNA and functional genes transcriptome", doctor, pp.2014
  16. Jin WW, "Characterization of bovine miRNAs by sequencing and bioinformatics analysis", BMC Mol Biol, 10, pp.90~ (2009)[DOI]
  17. Muroya S, "Profiling of differentially expressed microRNA and the bioinformatic target gene analyses in bovine fast-and slow-type muscles by massively parallel sequencing", J Anim Sci, 91, pp.90~130 (2013)[DOI]
  18. Zhang WW, "Effect of differentiation on microRNA expression in bovine skeletal muscle satellite cells by deep sequencing", Cell Mol Biol Lett, 21, pp.8~ (2016)[DOI]
  19. Sarjeant K, "Adipogenesis", Cold Spring Harb Perspect Biol, 4, pp.a008417~ (2012)[DOI]
  20. Xi FX, "MicroRNA-214-3p targeting Ctnnb1 promotes 3T3-L1 preadipocyte diferentiation by interfering with the Wnt", β-Catenin signaling pathway, 2019, pp.20, 1816~
  21. Sun GR, "gga-miRNA-18b-3p inhibits intramuscular adipocytes differentiation in chicken by targeting the ACOT13 gene", Cells, 8, pp.556~ (2019)[DOI]
  22. Li B, "miR-27a regulates sheep adipocyte differentiation by targeting CPT1B gene", Animals(Basel), 12, pp.28~ (2021)[DOI]
  23. Zhang Z, "miR-181a regulate porcine preadipocyte differentiation by targeting TGFBR1", Gene, 681, pp.45~51 (2019)[DOI]
  24. Yin CG, "Effect of castration on fatty deposition and the expression of related Genesin Yanbian yellow cattle(in Chinese with English abstract)", J Northeast Agric Sci, 44, pp.44~48 (2019)
  25. Hubler TR, "Intronic hormone response elements mediate regulation of FKBP5 by progestins and glucocorticoids", Cell Stress Chaperones, 9, pp.243~252 (2004)[DOI]
  26. Stechschulte LA, "FKBP51 null mice are resistant to diet-induced obesity and the PPARγ agonist rosiglitazone", Endocrinology, 157, pp.3888~3900 (2016)[DOI]
  27. Stechschulte LA, "FKBP51-a selective modulator of glucocorticoid and androgen sensitivity", Curr Opin Pharmacol, 11, pp.332~337 (2011)[DOI]
  28. Han JB, "mTORC1 signaling in hepatic lipid metabolism", Protein Cell, 9, pp.145~151 (2018)[DOI]
  29. Yang ZF, "An overview of the molecular mechanism of autophagy", Curr Top Microbiol Immunol, 335, pp.1~32 (2009)[DOI]
  30. Huang YJ, "mTOR signal pathway research progress in nutrition environment energy metabolism(in Chinese with English abstract)", Chin J Clin Res, 33, pp.244~248 (2020)

관련 논문AI추천

Screening of key miRNAs related with the differentiation of subcutaneous adipocytes and the validation of miR-133a-3p functional significance in goatsLin Yaqiu, Li Xin, Li Yanyan, Wang Yong, Wang Youli, Zhang Hao, Zhu Jiangjiang아세아·태평양축산학회 · Animal Bioscience2023 · 제36권 제1호Effect of gene CRTC2 on the differentiation of subcutaneous precursor adipocytes in goatsHu Tingting, Lin Yaqiu, Li Ruiwen, Liu Wei, Li Xuening, Li Yanyan, Wang Yong, Wang Youli아세아·태평양축산학회 · Animal Bioscience2025 · 제38권 제5호Effects of puerarin on the Akt signaling pathway in bovine preadipocyte differentiationGuoli Zhou, Hai-Guo Jin, Jinyan Yun, Xiaotong Luo, Yang Cao, Yongsheng Yu, Yumin Zhao아세아·태평양축산학회 · Animal Bioscience2020 · 제33권 제1호MicroRNA analysis reveals the role of miR-214 in duck adipocyte differentiationChang Guobin, Chen Guohong, Hu Xiaodan, Wang Laidi, Wang Shasha, Wang Zhixiu, Yuan Chunyou아세아·태평양축산학회 · Animal Bioscience2022 · 제35권 제9호Transcriptional regulation of porcine PABPN1 gene in adipogenesisChang Ming Hang, Gu Zhi Gang, Liu Ying Ke, Yang Si Qi, Yang Xiu Qin, Zhang Xiao Han, Zhao Xue Lian, Zhu Rong Ru아세아·태평양축산학회 · Animal Bioscience2025 · 제38권 제12호The cooperative regulatory effect of the miRNA-130 family on milk fat metabolism in dairy cowsChen Zhi, Gao Rui, Li Xiaofen, LUQINYUE, Lv Xiaoyang, Wu Yanni, Yang Xiaozhi아세아·태평양축산학회 · Animal Bioscience2024 · 제37권 제7호

이 간행물의 다른 논문 (15건)