Screening of key miRNAs related with the differentiation of subcutaneous adipocytes and the validation of miR-133a-3p functional significance in goats
6
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
Objective: Adipocyte differentiation is regulated by a variety of functional genes and noncoding RNAs. However, the role of miRNAs in lipid deposition of goat white adipose tissue is still unclear. Therefore, this study revealed the miRNA expression profile in goat subcutaneous adipocytes by sRNA-seq. Methods: The miRNA expressed in goat subcutaneous preadipocytes and the mature adipocytes were sequenced by sRNA-seq. The differentially expressed miRNAs (DEm) were screened and gene ontology (GO) and Kyoto encyclopedia for genes and genomes (KEGG) analyses were performed. Gain-of-function and loss-of-function combined with oil red O staining, Bodipy staining, and quantitative reverse-transcription polymerase chain reaction (qPCR) were utilized to determine the effect of miR-133a-3p on adipocyte differentiation. Results: A total of 218 DEm were screened out. The target genes of these DEm were significantly enriched in GO items such as biological regulation and in KEGG terms such as FAK signaling pathway and MAPK signaling pathway. qPCR verified that the expression trend of miRNA was consistent with miRNA-seq. The gain-of-function or loss-of-function of miR-133a-3p showed that it promoted or inhibited the accumulation of lipid droplets, and CCAAT enhancer binding protein α (C/EBPα) and C/EBPβ were extremely significantly up-regulated or down-regulated respectively (p<0.01), the loss-of-function also led to a significant down-regulation of peroxisome proliferator activated receptor gamma (PPARγ) (p<0.01). Conclusion: This study successfully identified miRNAs expression patterns in goat subcutaneous adipocytes, and functional identification indicates that miR-133a-3p is a positive regulator of the differentiation process of goat subcutaneous adipocytes. Our results lay the foundation for the molecular mechanism of lipid deposition in meat-source goats from the perspective of miRNA.
Abstract
Objective: Adipocyte differentiation is regulated by a variety of functional genes and noncoding RNAs. However, the role of miRNAs in lipid deposition of goat white adipose tissue is still unclear. Therefore, this study revealed the miRNA expression profile in goat subcutaneous adipocytes by sRNA-seq. Methods: The miRNA expressed in goat subcutaneous preadipocytes and the mature adipocytes were sequenced by sRNA-seq. The differentially expressed miRNAs (DEm) were screened and gene ontology (GO) and Kyoto encyclopedia for genes and genomes (KEGG) analyses were performed. Gain-of-function and loss-of-function combined with oil red O staining, Bodipy staining, and quantitative reverse-transcription polymerase chain reaction (qPCR) were utilized to determine the effect of miR-133a-3p on adipocyte differentiation. Results: A total of 218 DEm were screened out. The target genes of these DEm were significantly enriched in GO items such as biological regulation and in KEGG terms such as FAK signaling pathway and MAPK signaling pathway. qPCR verified that the expression trend of miRNA was consistent with miRNA-seq. The gain-of-function or loss-of-function of miR-133a-3p showed that it promoted or inhibited the accumulation of lipid droplets, and CCAAT enhancer binding protein α (C/EBPα) and C/EBPβ were extremely significantly up-regulated or down-regulated respectively (p<0.01), the loss-of-function also led to a significant down-regulation of peroxisome proliferator activated receptor gamma (PPARγ) (p<0.01). Conclusion: This study successfully identified miRNAs expression patterns in goat subcutaneous adipocytes, and functional identification indicates that miR-133a-3p is a positive regulator of the differentiation process of goat subcutaneous adipocytes. Our results lay the foundation for the molecular mechanism of lipid deposition in meat-source goats from the perspective of miRNA.
참고문헌 (43)
- Ripoll G, "Effect of rearing system on the straight and branched fatty acids of goat milk and meat of suckling kids", Foods, 9, pp.471~ (2020)[DOI]
- Watkins PJ, "Heptadecanoic acid as an indicator of BCFA content in sheep fat", Meat Sci, 151, pp.33~35 (2019)[DOI]
- Gregoire FM, "Understanding adipocyte differentiation", Physiol Rev, 78, pp.783~809 (1998)[DOI]
- Bartel DP, "MicroRNAs : genomics, biogenesis, mechanism, and function", Cell, 116, pp.281~297 (2004)[DOI]
- Ambros V, "The functions of animal microRNAs", Nature, 431, pp.350~355 (2004)[DOI]
- Ha M, "Regulation of microRNA biogenesis", Nat Rev Mol Cell Biol, 15, pp.509~524 (2014)[DOI]
- Sun YM, "PDGFRα Regulated by miR-34a and FoxO1 Promotes Adipogenesis in Porcine Intramuscular Preadipocytes through Erk Signaling Pathway", Int J Mol Sci, 18, pp.2424~ (2017)[DOI]
- Chen L, "microRNAs regulate adipocyte differentiation", Cell Biol Int, 37, pp.533~546 (2013)[DOI]
- Hu X, "MiR-27b impairs adipocyte differentiation of human adipose tissue-derived mesenchymal stem cells by targeting LPL", Cell Physiol Biochem, 47, pp.545~555 (2018)[DOI]
- Qi R, "MicroRNA-425 controls lipogenesis and lipolysis in adipocytes", Biochim Biophys Acta Mol Cell Biol Lipids, 1864, pp.744~755 (2019)[DOI]
- Zhang M, "Integrated analysis of MiRNA and genes associated with meat quality reveals that gga-mir-140-5p affects intramuscular fat deposition in chickens", Cell Physiol Biochem, 46, pp.2421~2433 (2018)[DOI]
- Hu Y, "A probabilistic framework for aligning paired-end RNA-seq data", Bioinformatics, 26, pp.1950~1957 (2010)[DOI]
- Li X, "RNA-seq analysis reveals the positive role of KLF5 in the differentiation of subcutaneous adipocyte in goats", Gene, 808, pp.145969~ (2022)[DOI]
- Peng Y, "MicroRNAs : emerging roles in adipogenesis and obesity", Cell Signal, 26, pp.1888~1896 (2014)[DOI]
- Wang Z, "RNA-Seq : a revolutionary tool for transcriptomics", Nat Rev Genet, 10, pp.57~63 (2009)[DOI]
- Bakhtiarizadeh MR, "Deep transcriptome analysis using RNA-Seq suggests novel insights into molecular aspects of fat-tail metabolism in sheep", Sci Rep, 9, pp.9203~ (2019)[DOI]
- Zhang Y, "Butyrate promotes slow-twitch myofiber formation and mitochondrial biogenesis in finishing pigs via inducing specific microRNAs and PGC-1α expression", J Anim Sci, 97, pp.3180~3192 (2019)[DOI]
- Wang L, "MiR-499-5p contributes to hepatic insulin resistance by suppressing PTEN", Cell Physiol Biochem, 36, pp.2357~2365 (2015)[DOI]
- Liu W, "miR-133a regulates adipocyte browning in vivo", PLoS Genet, 9, pp.e1003626~ (2013)[DOI]
- Liu H, "Inhibition of miR-499-5p expression improves nonalcoholic fatty liver disease", Ann Hum Genet (2020)
- Youssef EM, "Expression profiling and analysis of some miRNAs in subcutaneous white adipose tissue during development of obesity", Genes Nutr, 15, pp.8~ (2020)[DOI]
- Ning X, "Expression profiles and biological roles of miR-196a in swine", Genes(Basel), 7, pp.5~ (2016)[DOI]
- Mori M, "Essential role for miR-196a in brown adipogenesis of white fat progenitor cells", PLoS Biol, 10, pp.e1001314~ (2012)[DOI]
- Hou Y, "Transcriptome analysis of potential miRNA involved in adipogenic differentiation of C2C12myoblasts", Lipids, 53, pp.375~386 (2018)[DOI]
- Li JJ, "Cleavage of focal adhesion kinase(FAK)is essential in adipocyte differentiation", Biochem Biophys Res Commun, 357, pp.648~654 (2007)[DOI]
- Xiong Y, "LKB1 regulates goat intramuscular adipogenesis through focal adhesion pathway", Front Physiol, 12, pp.755598~ (2021)[DOI]
- Sakaue H, "Role of MAPK phosphatase-1(MKP-1)in adipocyte differentiation", J Biol Chem, 279, pp.39951~39957 (2004)[DOI]
- Wu W, "CTRP6 regulates porcine adipocyte proliferation and differentiation by the AdipoR1", MAPK signaling pathway, 2017, pp.65, 5512~5522
- Wang Q, "IL-27 signalling promotes adipocyte thermogenesis and energy expenditure", Nature, 600, pp.314~318 (2021)[DOI]
- Okla M, "Dietary factors promoting brown and beige fat development and thermogenesis", Adv Nutr, 8, pp.473~483 (2017)[DOI]
- Sakamoto T, "Dietary factors evoke thermogenesis in adipose tissues", Obes Res Clin Pract, 8, pp.e533~ (2014)[DOI]
- Rosen ED, "What we talk about when we talk about fat", Cell, 156, pp.20~44 (2014)[DOI]
- Zhang Y, "Irisin stimulates browning of white adipocytes through mitogen-activated protein kinase p38 MAP kinase and ERK MAP kinase signaling", Diabetes, 63, pp.514~525 (2014)[DOI]
- Song Z, "Calcium signaling pathways : key pathways in the regulation of obesity", Int J Mol Sci, 20, pp.2768~ (2019)[DOI]
- He YH, "The calcium-sensing receptor promotes adipocyte differentiation and adipogenesis through PPARγ pathway", Mol Cell Biochem, 361, pp.321~328 (2012)[DOI]
- Xiao J, "Hydrogen sulfide inhibits PCSK9 expression through the PI3K", Akt‑SREBP‑2 signaling pathway to influence lipid metabolism in HepG2 cells, 2019, pp.43, 2055~2063
- Song BQ, "Inhibition of notch signaling promotes the adipogenic differentiation of mesenchymal stem cells through autophagy activation and PTEN-PI3K", AKT, Cell Physiol Biochem, pp.2015, 36[DOI]
- Lee JH, "Fucosterol, isolated from Ecklonia stolonifera, inhibits adipogenesis through modulation of FoxO1 pathway in 3T3-L1 adipocytes", J Pharm Pharmacol, 69, pp.325~333 (2017)[DOI]
- Krycer JR, "Insulin signaling requires glucose to promote lipid anabolism in adipocytes", J Biol Chem, 295, pp.13250~13266 (2020)[DOI]
- Shan T, "Roles of notch signaling in adipocyte progenitor cells and mature adipocytes", J Cell Physiol, 232, pp.1258~1261 (2017)[DOI]
- Blüthgen N, "Systems analysis of MAPK signal transduction", Essays Biochem, 45, pp.95~108 (2008)[DOI]
- Han HJ, "Insulin stimulates Ca2+ uptake via PKC, cAMP, and p38 MAPK in mouse embryonic stem cells", Life Sci, 76, pp.2903~2919 (2005)[DOI]
- Oliveira MS, "UCP2, IL18, and miR-133a-3p are dysregulated in subcutaneous adipose tissue of patients with obesity", Mol Cell Endocrinol, 509, pp.110805~ (2020)[DOI]
