과제정보
This work was supported by the National Natural Science Foundation of China (Grant No. 32472885).
참고문헌
- Wang J, Khodabukus A, Rao L, Vandusen K, Abutaleb N, Bursac N. Engineered skeletal muscles for disease modeling and drug discovery. Biomaterials 2019;221:119416. https://doi.org/10.1016/j.biomaterials.2019.119416
- Weskamp K, Olwin BB, Parker R. Post-transcriptional regulation in skeletal muscle development, repair, and disease. Trends Mol Med 2021;27:469-81. https://doi.org/10.1016/j.molmed.2020.12.002
- Mo M, Zhang Z, Wang X, Shen W, Zhang L, Lin S. Molecular mechanisms underlying the impact of muscle fiber types on meat quality in livestock and poultry. Front Vet Sci 2023;10:1284551. https://doi.org/10.3389/fvets.2023.1284551
- Careccia G, Mangiavini L, Cirillo F. Regulation of satellite cells functions during skeletal muscle regeneration: a critical step in physiological and pathological conditions. Int J Mol Sci 2023;25:512. https://doi.org/10.3390/ijms25010512
- Addicks GC, Brun CE, Sincennes MC, et al. MLL1 is required for PAX7 expression and satellite cell self-renewal in mice. Nat Commun 2019;10:4256. https://doi.org/10.1038/s41467-019-12086-9
- Dumont NA, Bentzinger CF, Sincennes MC, Rudnicki MA. Satellite cells and skeletal muscle regeneration. Compr Physiol 2015;5:1027-59. https://dci.org/10.1002/cphy.c140068
- Zhao Y, Chen M, Lian D, et al. Non-coding RNA regulates the myogenesis of skeletal muscle satellite cells, injury repair and diseases. Cells 2019;8:988. https://doi.org/10.3390/cells8090988
- Liu S, Xie S, Chen H, et al. The functional analysis of transiently upregulated miR-101 suggests a 'braking' regulatory mechanism during myogenesis. Sci China Life Sci 2021;64:1612-23. https://doi.org/10.1007/s11427-020-1856-5
- Andresini O, Rossi MN, Matteini F, Petrai S, Santini T, Maione R. The long non-coding RNA Kcnq1ot1 controls maternal p57 expression in muscle cells by promoting H3K27me3 accumulation to an intragenic MyoD-binding region. Epigenetics Chromatin 2019;12:8. https://doi.org/10.1186/s13072-019-0253-1
- Chen SL, Wu CC, Li N, Weng TH. Post-transcriptional regulation of myogenic transcription factors during muscle development and pathogenesis. J Muscle Res Cell Motil 2024;45:21-39. https://doi.org/10.1007/s10974-023-09663-3
- Zheng T, Gan ML, Shen LY, et al. circRNA on animal skeletal muscle development regulation. Yi Chuan 2020;42:1178-91. https://doi.org/10.16288/j.yczz.20-207
- Chen L, Shan G. CircRNA in cancer: fundamental mechanism and clinical potential. Cancer Lett 2021;505:49-57. https://doi.org/10.1016/j.canlet.2021.02.004
- Misir S, Wu N, Yang BB. Specific expression and functions of circular RNAs. Cell Death Differ 2022;29:481-91. https://doi.org/10.1038/s41418-022-00948-7
- Huang K, Li Z, Zhong D, et al. A circular RNA generated from nebulin (NEB) gene splicing promotes skeletal muscle myogenesis in cattle as detected by a multi-omics approach. Adv Sci 2024;11:2300702. https://doi.org/10.1002/advs.
- Chen R, Yang T, Jin B, et al. CircTmeff1 promotes muscle atrophy by interacting with TDP-43 and encoding a novel TMEFF1-339aa protein. Adv Sci 2023;10:2206732. https://doi.org/10.1002/advs.202206732
- Yue B, Wang J, Song C, et al. Biogenesis and ceRNA role of circular RNAs in skeletal muscle myogenesis. Int J Biochem Cell Biol 2019;117:105621. https://doi.org/10.1016/j.biocel.2019.105621
- Li H, Yang J, Wei X, et al. CircFUT10 reduces proliferation and facilitates differentiation of myoblasts by sponging miR133a. J Cell Physiol 2018;233:4643-51. https://doi.org/10.1002/jcp.26230
- Chen M, Wei X, Song M, et al. Circular RNA circMYBPC1 promotes skeletal muscle differentiation by targeting MyHC. Mol Ther Nucleic Acids 2021;24:352-68. https://doi.org/10.1016/j.omtn.2021.03.004
- Yang Z, Song C, Jiang R, et al. CircNDSTl regulates bovine myoblasts proliferation and differentiation via the miR-411a/Smad4 axis. is Agric Food Chem 2022;70:10044-57. https://doi.org/10.1021/acs.jafc.1c08167
- Zhan S, Zhao W, Zhong T, et al. Role of circPAPD7 in regulating proliferation and differentiation of goat skeletal muscle satellite cells. Genomics 2024;116:110936. https://doi.org/10.1016/j.ygeno.2024.110936
- Salerno MS, Dyer K, Bracegirdle J, et al. Akirin1 (Mighty), a novel promyogenic factor regulates muscle regeneration and cell chemotaxis. Exp Cell Res 2009;315:2012-21. https://doi.org/10.1016/j.yexcr.2009.04.014
- Yan S, Pei Y, Li J, Tang Z, Yang Y. Recent progress on circular RNAs in the development of skeletal muscle and adipose tissues of farm animals. Biomolecules 2023;13:314. https://doi.org/10.3390/biom13020314
- Ru W, Qi A, Shen X, et al. The circular RNA circCPE regulates myoblast development by sponging miR-138. J Anim Sci Biotechnol 2021;12:102. https://doi.org/10.1186/s40104-021-00618-7
- Xing J, Qi X, Liu G, et al. A transcriptomic regulatory network among miRNAs, lncRNAs, circRNAs, and mRNAs associated with L-leucine-induced proliferation of equine satellite cells. Animals 2023;13:208. https://doi.org/10.3390/ani13020208
- Porpiglia E, Mai T, Kraft P, et al. Elevated CD47 is a hallmark of dysfunctional aged muscle stem cells that can be targeted to augment regeneration. Cell Stem Cell 2022;29:1653-68.E8. https://doi.org/10.1016/j.stem.2022.10.009
- Jung J, Wu Q. Identification of bone mineral density associated genes with shared genetic architectures across multiple tissues: functional insights for EPDR1, PKDCC, and SPTBN1. PLOS ONE 2024;19:e0300535. https://doi.org/10.1371/journal.pone.0300535
- Liu X, Liu C, Zhang A, et al. Long non-coding RNA SDCBP2-AS1 delays the progression of ovarian cancer via microRNA100-5p-targeted EPDR1. World J Surg Oncol 2021;19:199. https://doi.org/10.1186/s12957-021-02295-2
- Staats KA, Wu T, Gan BS, O'Gorman DB, Ophoff RA. Dupuytren's disease susceptibility gene, EPDR1, is involved in myofibroblast contractility. J Dermatol Sci 2016;83:131-7. https://doi.org/10.1016/j.jdermsci.2016.04.015
- Pippin JA, Chesi A, Wagley Y, et al. CRISPR Cas9–mediated genome editing confirms EPDR1 as an effector gene at the BMD GWAS implicated 'STARD3NL' locus. JBMR Plus 2021;5:e10531. https://doi.org/10.1002/jbm4.10531
- Pisignano G, Michael DC, Visal TH, Pirlog R, Ladomery M, Calin GA. Going circular: history, present, and future of circRNAs in cancer. Oncogene 2023;42:2783-800. https://doi.org/10.1038/s41388-023-02780-w
- Yan J, Yang Y, Fan X, et al. circRNAome profiling reveals circFgfr2 regulates myogenesis and muscle regeneration via a feedback loop. J Cachexia Sarcopenia Muscle 2022;13:696-712. https://doi.org/10.1002/jcsm.12859
- Liu J, Li M, Kong L, et al. CircARID1A regulates mouse skeletal muscle regeneration by functioning as a sponge of miR6368. FASEB J 2021;35:e21324. https://doi.org/10.1096/fj.202001992R
- Ouyang H, Chen X, Li W, Li Z, Nie Q, Zhang X. Circular RNA circSVIL promotes myoblast proliferation and differentiation by sponging miR-203 in chicken. Front Genet 2018;9:172. https://doi.org/10.3389/fgene.2018.00172
- Dong Y, Pan JS, Zhang L. Myostatin suppression of Akirin1 mediates glucocorticoid-induced satellite cell dysfunction. PLOS ONE 2013;8:e58554. https://doi.org/10.1371/journal.pone.0058554
- Zhang W, Liao Y, Shao P, et al. Integrated analysis of differently expressed microRNAs and mRNAs at different postnatal stages reveals intramuscular fat deposition regulation in goats (Capra hircus). Anim Genet 2024;55:238-48. https://doi.org/10.1111/age.13384
- Shu C, Xu P, Han J, Han S, He J. Upregulation of circRNA hsa_circ_0008726 in pre-eclampsia inhibits trophoblast migration, invasion, and EMT by regulating miR-345-3p/RYBP axis. Reprod Sci 2022;29:2829-41. https://doi.org/10.1007/s43032-021-00804-y
- Yang Y, Fan X, Mao M, et al. Extensive translation of circular RNAs driven by N6-methyladenosine. Cell Res 2017;27:626-41. https://doi.org/10.1038/cr.2017.31
- Xia H, Wu Y, Zhao J, et al. N6-methyladenosine-modified circSAV1 triggers ferroptosis in COPD through recruiting YTHDF1 to facilitate the translation of IREB2. Cell Death Differ 2023;30:1293-304. https://doi.org/10.1038/s41418-023-01138-9
- Li Y, Wang Z, Su P, et al. circ-EIF6 encodes EIF6-224aa to promote TNBC progression via stabilizing MYH9 and activating the Wnt/beta-catenin pathway. Mol Ther 2022;30:415-30. https://doi.org/10.1016/j.ymthe.2021.08.026
- Zhou B, Yang H, Yang C, et al. Translation of noncoding RNAs and cancer. Cancer Lett 2021;497:89-99. https://doi.org/10.1016/j.canlet.2020.10.002