Articles | Volume 64, issue 1
https://doi.org/10.5194/aab-64-17-2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/aab-64-17-2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
MiR-25-3p regulates the differentiation of intramuscular preadipocytes in goat via targeting KLF4
Yu Du
Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource
Reservation and Utilization, Ministry of Education, Southwest Minzu
University, Chengdu, China
Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and
Utilization Key Laboratory of Sichuan Province, College of Animal Science
and Veterinary Medicine, Chengdu, China
Institute of Qinghai-Tibetan Plateau, Chengdu 610041, China
Yue Zhao
Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource
Reservation and Utilization, Ministry of Education, Southwest Minzu
University, Chengdu, China
Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and
Utilization Key Laboratory of Sichuan Province, College of Animal Science
and Veterinary Medicine, Chengdu, China
Yong Wang
Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource
Reservation and Utilization, Ministry of Education, Southwest Minzu
University, Chengdu, China
Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and
Utilization Key Laboratory of Sichuan Province, College of Animal Science
and Veterinary Medicine, Chengdu, China
Qingyong Meng
State Key Laboratory of Agrobiotechnology, College of Biological
Sciences, China Agricultural University, Beijing 100193, China
Jiangjiang Zhu
Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource
Reservation and Utilization, Ministry of Education, Southwest Minzu
University, Chengdu, China
Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and
Utilization Key Laboratory of Sichuan Province, College of Animal Science
and Veterinary Medicine, Chengdu, China
Yaqiu Lin
CORRESPONDING AUTHOR
Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource
Reservation and Utilization, Ministry of Education, Southwest Minzu
University, Chengdu, China
Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and
Utilization Key Laboratory of Sichuan Province, College of Animal Science
and Veterinary Medicine, Chengdu, China
Related authors
No articles found.
Xin Li, Hao Zhang, Yong Wang, Yanyan Li, Yan Xiong, Ruiwen Li, Jiangjiang Zhu, and Yaqiu Lin
Arch. Anim. Breed., 65, 397–406, https://doi.org/10.5194/aab-65-397-2022, https://doi.org/10.5194/aab-65-397-2022, 2022
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The effect of STEAP4 (six-transmembrane epithelial antigen of the prostate 4) on goat adipocyte differentiation is unclear. We cloned the goat STEAP4 gene based on the Jianzhou Da’er goat and analyzed its properties and its expression in tissues and adipocytes; further, the positive effect on the expression of subcutaneous adipocytes was obvious. This study will provide a basis for elucidating the biological function of the STEAP4 gene in goat and provide a reference for goat molecular breeding.
Related subject area
Subject: DNA markers and gene expressions | Animal: Goats
Overexpression of goat STEAP4 promotes the differentiation of subcutaneous adipocytes
Meta-analysis of association between c.963A>G single-nucleotide polymorphism on BMP15 gene and litter size in goats
TIMP1 may affect goat prolificacy by regulating biological function of granulosa cells
CircRNA-0100 positively regulates the differentiation of cashmere goat SHF-SCs into hair follicle lineage via sequestering miR-153-3p to heighten the KLF5 expression
EDA and EDAR expression at different stages of hair follicle development in cashmere goats and effects on expression of related genes
Screening the key genes of hair follicle growth cycle in Inner Mongolian Cashmere goat based on RNA sequencing
A 20-bp insertion/deletion (indel) polymorphism within the CDC25A gene and its associations with growth traits in goat
Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
DNA methylation pattern of the goat PITX1 gene and its effects on milk performance
Genetic characterization of Markhoz goat breed using microsatellite markers
The novel 22 bp insertion mutation in a promoter region of the PITX2 gene is associated with litter size and growth traits in goats
Detection of insertion/deletions (indels) of the ATBF1 gene and their effects on growth-related traits in three indigenous goat breeds
Novel alternative splicing variants of ACOX1 and their differential expression patterns in goats
A novel 12 bp deletion within goat LHX4 gene significantly affected litter size
Xin Li, Hao Zhang, Yong Wang, Yanyan Li, Yan Xiong, Ruiwen Li, Jiangjiang Zhu, and Yaqiu Lin
Arch. Anim. Breed., 65, 397–406, https://doi.org/10.5194/aab-65-397-2022, https://doi.org/10.5194/aab-65-397-2022, 2022
Short summary
Short summary
The effect of STEAP4 (six-transmembrane epithelial antigen of the prostate 4) on goat adipocyte differentiation is unclear. We cloned the goat STEAP4 gene based on the Jianzhou Da’er goat and analyzed its properties and its expression in tissues and adipocytes; further, the positive effect on the expression of subcutaneous adipocytes was obvious. This study will provide a basis for elucidating the biological function of the STEAP4 gene in goat and provide a reference for goat molecular breeding.
Emel Zergani, Amir Rashidi, Jalal Rostamzadeh, Mohammad Razmkabir, and Jens Tetens
Arch. Anim. Breed., 65, 309–318, https://doi.org/10.5194/aab-65-309-2022, https://doi.org/10.5194/aab-65-309-2022, 2022
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Different studies have reported controversial results regarding the effects of c.963A>G polymorphism in the BMP15 gene on litter size in goats. We conducted a meta-analysis by using data of all published relevant studies to address this contradiction and found a significant association between c.963A>G polymorphism and litter size at birth under dominant and additive genetic models. The meta-analysis results revealed that the AA genotype could be positively connected with litter size in goats.
Lei Hong, Xiang Chen, Min Zhu, Zheng Ao, Wen Tang, and Zhinan Zhou
Arch. Anim. Breed., 65, 105–111, https://doi.org/10.5194/aab-65-105-2022, https://doi.org/10.5194/aab-65-105-2022, 2022
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Tissue inhibitor of metalloproteinase 1 (TIMP1) plays a crucial role in follicle growth and embryonic development. Ovarian granulosa cells also play an essential role in these processes. However, the effect of TIMP1 on the biological function of goat ovarian granulosa cells remains unknown. The objective of this study was to explore the impact of TIMP1 on granulosa cell proliferation and reproductive characteristics in goats.
Junyin Zhao, Jincheng Shen, Zeying Wang, Man Bai, Yixing Fan, Yubo Zhu, and Wenlin Bai
Arch. Anim. Breed., 65, 55–67, https://doi.org/10.5194/aab-65-55-2022, https://doi.org/10.5194/aab-65-55-2022, 2022
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Cashmere is a natural fiber from cashmere goats. The textile has been favored by consumers due to typical features like lightness, softness, and comfort. In this study, we show that circRNA-0100 promotes the differentiation of secondary hair follicle stem cells into hair lineage via sequestering miR-153-3p to heighten the KLF5 expression. Our results provide significant information for artificially regulating the secondary hair follicle regeneration and cashmere growth in cashmere goats.
Zhihong Wu, Yu Wang, Wenjing Han, Kun Yang, Erhan Hai, Rong Ma, Zhengyang Di, Fangzheng Shang, Rui Su, Ruijun Wang, Zhiying Wang, Yanjun Zhang, and Jinquan Li
Arch. Anim. Breed., 63, 461–470, https://doi.org/10.5194/aab-63-461-2020, https://doi.org/10.5194/aab-63-461-2020, 2020
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This study provided a theoretical and experimental basis for further studying the molecular regulation mechanism of hair follicle development. EDA and EDAR were both expressed in the skin tissue in the seven cashmere goat embryo stages. Moreover, EDA and EDAR play an important role in the formation of embryonic placode (Pc). After interfering with EDA and EDAR, the expression of BMP2, BMP4, noggin, β-catenin, TGF-β2, Wnt-10b, and NOTCH1 in fibroblasts and epithelial cells changed significantly.
Rui Su, Gao Gong, Lingtian Zhang, Xiaochun Yan, Fenghong Wang, Lei Zhang, Xian Qiao, Xiaokai Li, and Jinquan Li
Arch. Anim. Breed., 63, 155–164, https://doi.org/10.5194/aab-63-155-2020, https://doi.org/10.5194/aab-63-155-2020, 2020
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We tried to find important influencing factors of SHF growth cycle in skin tissue from Inner Mongolian Cashmere goats by RNA sequencing (RNA-Seq). Based on the results of comprehensive analysis of differentially expressed genes, GO enrichment and KEGG enrichment, we found that FGF5, FGFR1 and RRAS had an effect on the hair follicle growth cycle. The results of this study may provide a theoretical basis for further research on the growth and development of SHF in Inner Mongolian Cashmere goats.
Wenbo Cui, Nuan Liu, Xuelian Zhang, Yanghai Zhang, Lei Qu, Hailong Yan, Xianyong Lan, Wuzi Dong, and Chuanying Pan
Arch. Anim. Breed., 62, 353–360, https://doi.org/10.5194/aab-62-353-2019, https://doi.org/10.5194/aab-62-353-2019, 2019
Mengli Zhao, Huitong Zhou, Jon G. H. Hickford, Hua Gong, Jiqing Wang, Jiang Hu, Xiu Liu, Shaobin Li, Zhiyun Hao, and Yuzhu Luo
Arch. Anim. Breed., 62, 125–133, https://doi.org/10.5194/aab-62-125-2019, https://doi.org/10.5194/aab-62-125-2019, 2019
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Keratin-associated proteins (KAPs) are a structural component of cashmere fibre, and variation in some KAP genes (KRTAPs) has been associated with a number of caprine fibre traits. In this study, we identified the caprine KAP15-1 gene on goat chromosome 1. Six variants containing eight SNPs were found. Association analyses revealed that variation in the gene affected mean fibre diameter.
Haiyu Zhao, Sihuan Zhang, Xianfeng Wu, Chuanying Pan, Xiangchen Li, Chuzhao Lei, Hong Chen, and Xianyong Lan
Arch. Anim. Breed., 62, 59–68, https://doi.org/10.5194/aab-62-59-2019, https://doi.org/10.5194/aab-62-59-2019, 2019
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This study analyzed the DNA methylation profile of the PITX1 gene and its relevance to lactation performance in goats. The methylation rates of the overall CpG island and the 3rd and 12th CpG-dinucleotide loci in blood were significantly associated with average milk yield. The overall methylation rates of the CpG island in mammary gland tissue from dry and lactation periods showed a significant difference. These results could be used as potential epigenetic markers for lactation performance.
Fariborz Asroush, Seyed-Ziaeddin Mirhoseini, Nejat Badbarin, Alireza Seidavi, Vincenzo Tufarelli, Vito Laudadio, Cataldo Dario, and Maria Selvaggi
Arch. Anim. Breed., 61, 469–473, https://doi.org/10.5194/aab-61-469-2018, https://doi.org/10.5194/aab-61-469-2018, 2018
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The study aimed to genetically characterize Markhoz goat breed using specific microsatellite markers to investigate the genetic diversity within this population and to enhance future breeding strategies and conservation programmes. From findings, despite the decreasing population size, Markhoz goat genetic diversity seems still conserved and the breed seems to have a good level of genetic variability as well as a potential margin of adaptability to environment and future genetic improvement.
Hailong Yan, Enhui Jiang, Haijing Zhu, Linyong Hu, Jinwang Liu, and Lei Qu
Arch. Anim. Breed., 61, 329–336, https://doi.org/10.5194/aab-61-329-2018, https://doi.org/10.5194/aab-61-329-2018, 2018
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As we all know, genes often influence physiological functions of animal organisms such as reproduction, growth, and development. This study explored a novel insertion of paired-like homeodomain 2 (PITX2) gene, and many methods of statistical analysis were used to evaluate their associations with traits of goats. Results indicated that this insertion was significantly associated with litter size, body length, and chest width of goats.
Zhenyu Wei, Ke Wang, Yiqing Hui, Hailong Yan, Haijing Zhu, Lei Qu, Chuanying Pan, Hong Chen, and Xianyong Lan
Arch. Anim. Breed., 61, 311–319, https://doi.org/10.5194/aab-61-311-2018, https://doi.org/10.5194/aab-61-311-2018, 2018
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An effective DNA marker-assisted selection would speed up the development and improvement of goat products. The objective of this work was to explore novel indel (insertion/deletion) variations and their associations with growth traits in three native Chinese goat breeds. Results showed that the goat ATBF1 gene had marked effects on growth traits and the growth-trait-related loci, which would contribute to improving the growth-related traits of local breeds in the goat industry.
Xian-Feng Wu, Yuan Liu, Cheng-Fang Gao, Xin-Zhu Chen, Xiao-Pei Zhang, and Wen-Yang Li
Arch. Anim. Breed., 61, 59–70, https://doi.org/10.5194/aab-61-59-2018, https://doi.org/10.5194/aab-61-59-2018, 2018
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ACOX1 is vital for fatty acid oxidation and deposition. The alternative splicing events of ACOX1 have not been reported in goats. Here, we found a novel splice variant (ACOX1-SV1) and a complete isoform (ACOX1). ACOX1 and ACOX1-SV1 were expressed at high levels in the liver, spleen, brain and fat in kid and adult goats. In both groups, the mRNA level of ACOX1 was high in fat and that of ACOX1-SV1 was high in liver. These findings should provide new insights on the function of ACOX1.
Hailong Yan, Fei Zhang, Ke Wang, Jinwang Liu, Haijing Zhu, Chuanying Pan, and Lei Qu
Arch. Anim. Breed., 61, 1–8, https://doi.org/10.5194/aab-61-1-2018, https://doi.org/10.5194/aab-61-1-2018, 2018
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In this study, a novel 12 bp indel within the LHX4 gene first intron was firstly found. Meanwhile, the association analysis indicated that the 12 bp indel was significantly associated with litter size in 1149 Shaanbei cashmere goats (P < 0.05). The litter sizes of genotype DD and ID individuals were superior to those of genotype II, implying that the 12 bp indel might affect litter size. These results could provide a new insight into implementing marker-assisted selection in goat breeding.
Cited articles
Acharya, A., Berry, D. C., Zhang, H., Jiang, Y., Jones, B. T., Hammer, R.
E., Graff, J. M., and Mendell, J. T.: MiR-26 suppresses adipocyte progenitor
differentiation and fat production by targeting Fbxl19, Gene. Dev., 33,
1367–1380, https://doi.org/10.1101/gad.328955.119, 2019.
Anna, E., Shannon, H. C., Hillary J. C., Melissa, F., Noyan, G., and Katya,
R.: An adenosine receptor-Krüppel-like factor 4 protein axis inhibits
adipogenesis, J. Biol. Chem., 289, 21071–21081, https://doi.org/10.1074/jbc.M114.566406, 2014.
Chen, T., Cui, J., Ma, L., Zeng, Y., and Chen, W.: The Effect of
MicroRNA-331-3p on Preadipocytes Proliferation and Differentiation and Fatty
Acid Accumulation in Laiwu Pigs, Biomed. Res. Int., 2019, 9287804,
https://doi.org/10.1155/2019/9287804, 2019.
Cui, J., Chen, W., Liu, J., Xu, T., and Zeng, Y.: Study on quantitative
expression of PPARγ and ADRP in muscle and its association with
intramuscular fat deposition of pig, SpringerPlus, 5, 1501,
https://doi.org/10.1186/s40064-016-3187-0, 2016.
Edwards, P. A., Tabor, D., Kast, H. R., and Venkateswaran, A.: Regulation of
gene expression by SREBP and SCAP, Biochim Biophys Acta, 1529, 103–113,
https://doi.org/10.1016/s1388-1981(00)00140-2, 2000.
Engin, A. B.: MicroRNA and Adipogenesis, Adv. Exp. Med. Biol., 960, 489–509,
https://doi.org/10.1007/978-3-319-48382-5_21, 2017.
Feng, S. J., Pan, W. J., Jin, Y., and Zheng, J. H.: MiR-25 promotes ovarian
cancer proliferation and motility by targeting LATS2, Tumour Biol., 35,
12339-12344, https://doi.org/10.1007/s13277-014-2546-0, 2014.
Grieco, G. E., Brusco, N., Licata, G., Nigi, L., Formichi, C.,
Dotta, F., and Sebastiani, G.: Targeting microRNAs as a Therapeutic Strategy to
Reduce Oxidative Stress in Diabetes, Int. J. Mol. Sci., 20, 6358,
https://doi.org/10.3390/ijms20246358, 2019.
Irani, S. and Hussain, M. M.: Role of microRNA-30c in lipid metabolism,
adipogenesis, cardiac remodeling and cancer, Curr. Opin. Lipidol., 26,
139–146, https://doi.org/10.1097/MOL.0000000000000162, 2015.
Jeon, Y. G., Lee, J. H., Ji, Y., Sohn, J. H., Lee, D., Kim, D. W., Yoon, S.
G., Shin, K. C., Park, J., Seong, J. K., Cho, J.-Y., Choe, S. S., and Kim,
J. B.: RNF20 Functions as a Transcriptional Coactivator for PPARγ by
Promoting NCoR1 Degradation in Adipocytes, Diabetes, 69, 20–34,
https://doi.org/10.2337/db19-0508, 2020.
Jiang, Q., Sun, B., Liu, Q., Cai, M., Wu, R., Wang, F., Yao, Y., Wang, Y.,
and Wang, X.: MTCH2 promotes adipogenesis in intramuscular preadipocytes via
an m6A-YTHDF1-dependent mechanism, FASEB J., 33, 2971–2981, https://doi.org/10.1096/fj.201801393RRR,
2019.
Lee, D. S., Choi, H., Han, B. S., Kim, W. K., Lee, S. C., Oh, K.-J., and
Bae, K.-H.: C-Jun regulates adipocyte differentiation via the KLF15-mediated
mode, Biochem. Biophys. Res. Commun., 469, 552–558,
https://doi.org/10.1016/j.bbrc.2015.12.035, 2016.
Liang, W. C., Wang, Y., Liang, P. P., Pan, X. Q., Fu, W. M., Yeung, V. S.
Y., Lu, Y. F., Wan, D. C. C., Tsui, S. K. W., Tsang, S. Y., Ma, W. B.,
Zhang, J. F., and Waye, M. M. Y.: MiR-25 suppresses 3T3-L1 adipogenesis by
directly targeting KLF4 and C/EBPα, J. Cell Biochem., 116, 2658–2666,
https://doi.org/10.1002/jcb.25214, 2015.
Lin, S.: Regulation of KLF4 on intramuscular preadipocyte differentiation in goat, Southwest Minzu University, available at: https://kns.cnki.net/kns8?dbcode=CDMD (last access: 7 January 2021), 2018.
Lin, Z., He, H., Wang, M., and Liang, J.: MicroRNA-130a controls bone marrow
mesenchymal stem cell differentiation towards the osteoblastic and
adipogenic fate, Cell Prolif., 52, e12688,
https://doi.org/10.1111/cpr.12688, 2019.
Ma, C., Xia, R., Yang, S., Liu, L., Zhang, J., Feng, K., Shang, Y., Qu, J.,
Li, L., Chen, N., Xu, S., Zhang, W., Mao, J., Han, J., Chen, Y., Yang, X.,
Duan, Y., and Fan, G.: Formononetin attenuates atherosclerosis via regulating
interaction between KLF4 and SRA in apoE-/-mice, Theranostics, 10,
1090–1106, https://doi.org/10.7150/thno.38115, 2020.
Ma, L., Qiu, H., Chen, Z., Li, L., Zeng, Y., Luo, J., and Gou, D.: MiR-25
modulates triacylglycerol and lipid accumulation in goat mammary epithelial
cells by repressing PGC-1beta, J. Anim. Sci. Biotechnol., 9, 48,
https://doi.org/10.1186/s40104-018-0262-0, 2018.
Moon, Y. A., Shah, N. A., Mohapatra, S., Warrington, J. A., and Horton, J.
D.: Identification of a mammalian long chain fatty acyl elongase regulated by
sterol regulatory element-binding proteins, J. Biol. Chem., 276, 45358–45366, https://doi.org/10.1074/jbc.M108413200, 2001.
Nimonkar, A. V., Weldon, S., Godbout, K., Panza, D., Hanrahan, S., Cubbon,
R., Xu, F., Trauger, J. W., Gao, J., and Voznesensky, A.: A lipoprotein
lipase-GPI-anchored high-density lipoprotein-binding protein 1 fusion lowers
triglycerides in mice: Implications for managing familial chylomicronemia
syndrome, J. Biol. Chem., 295, 2900–2912, https://doi.org/10.1074/jbc.RA119.011079,
2020.
Pérez-Torres, I., Gutiérrez-Alvarez, Y., Guarner-Lans, V.,
Díaz-Díaz, E., Manzano Pech, L., and Caballero-Chacón, S. D.
C.: Intra-Abdominal Fat Adipocyte Hypertrophy through a Progressive
Alteration of Lipolysis and Lipogenesis in Metabolic Syndrome Rats,
Nutrients, 11, 1529, https://doi.org/10.3390/nu11071529, 2019.
Poleti, M. D., Regitano, L. C. A., Souza, G. H. M. F., Cesar, A. S. M.,
Simas, R. C., Silva-Vignato, B., Oliveira, G. B., Andrade, S. C. S.,
Cameron, L. C., and Coutinho, L. L.: Longissimus dorsi muscle label-free
quantitative proteomic reveals biological mechanisms associated with
intramuscular fat deposition, J Proteomics., 179, 30–41,
https://doi.org/10.1016/j.jprot.2018.02.028, 2018a.
Poleti, M. D., Regitano, L. C. A., Souza, G. H. M. F., Cesar, A. S. M.,
Simas, R. C., Silva-Vignato, B., Oliveira, G. B., Andrade, S. C. S.,
Cameron, L. C., and Coutinho, L. L.: Data from proteomic analysis of bovine
Longissimus dorsi muscle associated with intramuscular fat content, Data
Brief., 19, 1314–1317, https://doi.org/10.1016/j.dib.2018.06.004, 2018b.
Qi, R., Wang, J., Wang, Q., Qiu, X., Yang, F., Liu, Z., and Huang, J.:
MicroRNA-425 controls lipogenesis and lipolysis in adipocytes, BBA-Mol. Cell Biol. L., 1864, 744–755,
https://doi.org/10.1016/j.bbalip.2019.02.007, 2019.
Rao, X., Huang, X., Zhou, Z., and Lin, X.: An improvement of the 2−ΔΔCT method for quantitative real-time polymerase chain
reaction data analysis, Biostat Bioinforma Biomath., 3, 71–85,
2013.
Ren, L.: Biological Function Studies of Candidate Genes S100A10 and
Bta-miR-210 Related to Intramuscular Fat Deposition in Cattle, Chinese
Academy of Agricultural Sciences, available at: https://kns.cnki.net/kns8?dbcode=CDMD (last access: 7 January 2021), 2019.
Ruppert, P. M. M. and Kersten, S.: A lipase fusion feasts on fat, J. Biol.
Chem., 295, 2913–2914, https://doi.org/10.1074/jbc.H120.012744, 2020.
Semo, J., Chernin, G., Jonas, M., Shimoni, S., and George, J.: Deletion of
the Mir-106b∼25 MicroRNA cluster attenuates atherosclerosis
in Apolipoprotein E knockout mice, Lipids Health Dis., 18, 208,
https://doi.org/10.1186/s12944-019-1155-8, 2019.
Shang, Z. C., Guo, L., Wang, N., Shi, H., Wang, Y. X., and Li, H.: Oleate
promotes differentiation of chicken primary preadipocytes in vitro, Biosci.
Rep., 34, 00093, https://doi.org/10.1042/BSR20130120, 2014.
Shi, H., Luo, J., Zhu, J., Li, J., Sun, Y., Lin, X., Zhang, L., Yao, D., and
Shi, H.: PPAR γ Regulates Genes Involved in Triacylglycerol Synthesis
and Secretion in Mammary Gland Epithelial Cells of Dairy Goats, PPAR Res.,
2013, 310948, https://doi.org/10.1155/2013/310948, 2013.
Son, Y. H., Ka, S., Kim, A. Y., and Kim, J. B.: Regulation of Adipocyte
Differentiation via MicroRNAs. Endocrinol Metab (Seoul), 29, 122–135,
https://doi.org/10.3803/EnM.2014.29.2.122, 2014.
Sun, G. R., Zhang, M., Sun, J. W., Li, F., Ma, X. F., Li, W. T., Han, R. L., Li,
Z. J., Jiang, R. R., Li, G. X., Yan, F. B., and Kang, X. T.: Krüppel-like
factor KLF9 inhibits chicken intramuscular preadipocyte differentiation, Brit.
Poultry Sci., 60, 790–797, https://doi.org/10.1080/00071668.2019.1657229,
2019.
Wood, J. D., Enser, M., Fisher, A. V., Nute, G. R., Sheard, P. R.,
Richardson, R. I., Hughes, S. I., and Whittington, F. M. Fat deposition,
fatty acid composition and meat quality: A review, Meat Sci., 78, 343–358,
https://doi.org/10.1016/j.meatsci.2007.07.019, 2008.
Xiang, J., Hang, J. B., Che, J. M., and Li, H. C.: MiR-25 is up-regulated in
non-small cell lung cancer and promotes cell proliferation and motility by
targeting FBXW7, Int. J. Clin. Exp. Pathol., 8, 9147–9153,
2015.
Xu, Q., Lin, S., Li, Q., Lin, Y., Xiong, Y., Zhu, J., and Wang, Y.:
Fibroblast growth factor 21 regulates lipid accumulation and adipogenesis in
goat intramuscular adipocyte, Anim Biotechnol., 27, 1–9,
https://doi.org/10.1080/10495398.2019.1691010, 2019.
Xu, Q., Lin, S., Wang, Y., Zhu, J., and Lin, Y.: Fibroblast growth factor 10
(FGF10) promotes the adipogenesis of intramuscular preadipocytes in goat,
Mol. Biol. Rep., 45, 1881–1888, https://doi.org/10.1007/s11033-018-4334-1,
2018.
Yang, N., Li, C., Li, H., Liu, M., Cai, X., Cao, F., Feng, Y., Li, M., and
Wang, X.: Emodin Induced SREBP1-Dependent and SREBP1-Independent Apoptosis in
Hepatocellular Carcinoma Cells, Front Pharmacol., 10, 709,
https://doi.org/10.3389/fphar.2019.00709, 2019.
Zaiou, M., El Amri, H., and Bakillah, A.: The clinical potential of
adipogenesis and obesity-related microRNAs, Nutr. Metab. Cardiovasc. Dis., 28,
91–111, https://doi.org/10.1016/j.numecd.2017.10.015, 2018.
Zeng, Z., Li, Y., Pan, Y., Lan, X., Song, F., Sun, J., Zhou, K., Liu, X.,
Ren, X., Wang, F., Hu, J., Zhu, X., Yang, W., Liao, W., Li, G., Ding, Y.,
and Liang, L.: Cancer-derived exosomal miR-25-3p promotes pre-metastatic
niche formation by inducing vascular permeability and angiogenesis, Nat.
Commun., 9, 5395, https://doi.org/10.1038/s41467-018-07810-w, 2018.
Zhang, H. Y., Zuo, Z., Lu, X., Wang, H. Y., and Zhu, Z. L.: MiR-25 regulates
apoptosis by targeting Bim in human ovarian cancer, Oncol Rep., 27, 594–598,
https://doi.org/10.3892/or.2011.1530, 2012.
Zhang, Y., Zhou, L., Zhang, Z., Xu, Q., Han, X., Zhao, Y., Song, X., Zhao,
T., and Ye, L.: Effects of di (2-ethylhexyl) phthalate and high-fat diet on
lipid metabolism in rats by JAK2/STAT5, Environ. Sci. Pollut. R. Int., 27,
3837–3848, https://doi.org/10.1007/s11356-019-06599-5, 2019.
Zhao, X., Chen, S., Tan, Z., Wang, Y., Zhang, F., Yang, T., Liu, Y., Ao, H.,
Xing, K., and Wang, C.: Transcriptome Analysis of Landrace Pig Subcutaneous
Preadipocytes during Adipogenic Differentiation, Genes (Basel), 10, 552, https://doi.org/10.3390/genes10070552,
2019.
Zhao, Y.: Study on miR-142 and miR-144 Down-Regulation Contributions to Differentiation of Ovine Rreadipocytes by Targeting FoxO1 Gene, Shanxi Agricultural University, available at: https://kns.cnki.net/kns8?dbcode=CDMD (last access: 7 January 2021), 2018.
Zhou, P., Xu, W., Peng, X., Luo, Z., Xing, Q., Chen, X., Hou, C., Liang, W.,
Zhou, J., Wu, X., Songyang, Z., and Jiang, S.: Large-scale screens of
miRNA-mRNA interactions unveiled that the 3′UTR of a gene is targeted by
multiple miRNAs, PloS One, 8, e68204,
https://doi.org/10.1371/journal.pone.0068204, 2013.
Short summary
Intramuscular fat is a type of fatty tissue deposited between skeletal muscle fibers and muscle bundles, which is regulated by the number and size of preadipocytes in the muscle, and it is a key factor affecting meat tenderness and juiciness. As a member of miRNAs, a variety of studies suggested that miR-25-3p may play an important role in regulating lipid metabolism and adipocyte differentiation. This study attempts to investigate the role of miR-25-3p in goat intramuscular preadipocytes.
Intramuscular fat is a type of fatty tissue deposited between skeletal muscle fibers and muscle...