• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
MicroRNA-378 targets the myogenic repressor MyoR during myoblast differentiation.微小 RNA-378 在成肌细胞分化过程中靶向肌生成抑制因子 MyoR。
J Biol Chem. 2011 Jun 3;286(22):19431-8. doi: 10.1074/jbc.M111.219006. Epub 2011 Apr 6.
2
miR-206 and -486 induce myoblast differentiation by downregulating Pax7.miR-206 和 -486 通过下调 Pax7 诱导成肌细胞分化。
Mol Cell Biol. 2011 Jan;31(1):203-14. doi: 10.1128/MCB.01009-10. Epub 2010 Nov 1.
3
A novel target of microRNA-29, Ring1 and YY1-binding protein (Rybp), negatively regulates skeletal myogenesis.miRNA-29 的新靶标,环状 RNA 结合蛋白(Rybp),负调控骨骼肌生成。
J Biol Chem. 2012 Jul 20;287(30):25255-65. doi: 10.1074/jbc.M112.357053. Epub 2012 May 31.
4
MicroRNA-148a promotes myogenic differentiation by targeting the ROCK1 gene.MicroRNA-148a 通过靶向 ROCK1 基因促进成肌分化。
J Biol Chem. 2012 Jun 15;287(25):21093-101. doi: 10.1074/jbc.M111.330381. Epub 2012 Apr 30.
5
Mir-214-dependent regulation of the polycomb protein Ezh2 in skeletal muscle and embryonic stem cells.骨骼肌和胚胎干细胞中mir-214对多梳蛋白Ezh2的依赖性调控
Mol Cell. 2009 Oct 9;36(1):61-74. doi: 10.1016/j.molcel.2009.08.008.
6
MiR-501-3p Forms a Feedback Loop with FOS, MDFI, and MyoD to Regulate C2C12 Myogenesis.miR-501-3p 与 FOS、MDFI 和 MyoD 形成反馈环路调节 C2C12 成肌分化。
Cells. 2019 Jun 11;8(6):573. doi: 10.3390/cells8060573.
7
MyoD directly up-regulates premyogenic mesoderm factors during induction of skeletal myogenesis in stem cells.MyoD 在干细胞的成骨肌发生诱导过程中直接上调前生肌间充质因子。
J Biol Chem. 2011 Jan 28;286(4):2517-25. doi: 10.1074/jbc.M110.163709. Epub 2010 Nov 15.
8
Inhibition of miR-29 by TGF-beta-Smad3 signaling through dual mechanisms promotes transdifferentiation of mouse myoblasts into myofibroblasts.TGF-β-Smad3 信号通过双重机制抑制 miR-29 促进小鼠成肌细胞向肌成纤维细胞的转分化。
PLoS One. 2012;7(3):e33766. doi: 10.1371/journal.pone.0033766. Epub 2012 Mar 16.
9
MyoR: a muscle-restricted basic helix-loop-helix transcription factor that antagonizes the actions of MyoD.MyoR:一种肌肉特异性的碱性螺旋-环-螺旋转录因子,可拮抗MyoD的作用。
Proc Natl Acad Sci U S A. 1999 Jan 19;96(2):552-7. doi: 10.1073/pnas.96.2.552.
10
miR-155 inhibits expression of the MEF2A protein to repress skeletal muscle differentiation.miR-155 通过抑制 MEF2A 蛋白的表达来抑制骨骼肌分化。
J Biol Chem. 2011 Oct 14;286(41):35339-35346. doi: 10.1074/jbc.M111.273276. Epub 2011 Aug 25.

引用本文的文献

1
MicroRNAs at the crossroads of exercise and ferroptosis: a regulatory bridge.运动与铁死亡交叉点上的微小RNA:一座调控桥梁
Clin Exp Med. 2025 Jul 6;25(1):234. doi: 10.1007/s10238-025-01766-0.
2
Exosomes and microRNAs as mediators of the exercise.外泌体和微小RNA作为运动的介质。
Eur J Med Res. 2025 Jan 19;30(1):38. doi: 10.1186/s40001-025-02273-4.
3
Comparative analysis of the whole transcriptome landscapes of muscle and adipose tissue in Qinchuan beef cattle.秦川肉牛肌肉和脂肪组织全转录组图谱的比较分析
BMC Genomics. 2025 Jan 14;26(1):32. doi: 10.1186/s12864-025-11223-7.
4
Ythdf2 facilitates precursor miR-378/miR-378-5p maturation to support myogenic differentiation.Ythdf2 促进前体 miR-378/miR-378-5p 的成熟以支持成肌分化。
Cell Mol Life Sci. 2024 Nov 6;81(1):445. doi: 10.1007/s00018-024-05456-0.
5
The Role of Non-Coding RNAs in Regulating Cachexia Muscle Atrophy.非编码 RNA 在调控恶病质肌肉萎缩中的作用。
Cells. 2024 Sep 27;13(19):1620. doi: 10.3390/cells13191620.
6
Epigenetics of Skeletal Muscle Atrophy.骨骼肌萎缩的表观遗传学
Int J Mol Sci. 2024 Jul 31;25(15):8362. doi: 10.3390/ijms25158362.
7
The effects of exercise on epigenetic modifications: focus on DNA methylation, histone modifications and non-coding RNAs.运动对表观遗传修饰的影响:聚焦于 DNA 甲基化、组蛋白修饰和非编码 RNA。
Hum Cell. 2024 Jul;37(4):887-903. doi: 10.1007/s13577-024-01057-y. Epub 2024 Apr 8.
8
Regulation of myo-miR-24-3p on the Myogenesis and Fiber Type Transformation of Skeletal Muscle.肌源性 miR-24-3p 对骨骼肌成肌和纤维类型转换的调控。
Genes (Basel). 2024 Feb 21;15(3):269. doi: 10.3390/genes15030269.
9
Post-transcriptional regulation of myogenic transcription factors during muscle development and pathogenesis.肌肉发育和发病机制中肌源性转录因子的转录后调控。
J Muscle Res Cell Motil. 2024 Mar;45(1):21-39. doi: 10.1007/s10974-023-09663-3. Epub 2024 Jan 11.
10
Integrated Transcriptome Analysis of miRNAs and mRNAs in the Skeletal Muscle of Wuranke Sheep.乌冉克羊骨骼肌中 miRNA 和 mRNA 的整合转录组分析。
Genes (Basel). 2023 Oct 31;14(11):2034. doi: 10.3390/genes14112034.

本文引用的文献

1
miR-206 and -486 induce myoblast differentiation by downregulating Pax7.miR-206 和 -486 通过下调 Pax7 诱导成肌细胞分化。
Mol Cell Biol. 2011 Jan;31(1):203-14. doi: 10.1128/MCB.01009-10. Epub 2010 Nov 1.
2
MyoD regulates apoptosis of myoblasts through microRNA-mediated down-regulation of Pax3.MyoD 通过 microRNA 介导的下调 Pax3 调控成肌细胞的凋亡。
J Cell Biol. 2010 Oct 18;191(2):347-65. doi: 10.1083/jcb.201006025.
3
microRNA-1 and microRNA-206 regulate skeletal muscle satellite cell proliferation and differentiation by repressing Pax7.miRNA-1 和 miRNA-206 通过抑制 Pax7 来调节骨骼肌卫星细胞的增殖和分化。
J Cell Biol. 2010 Sep 6;190(5):867-79. doi: 10.1083/jcb.200911036.
4
Mammalian microRNAs predominantly act to decrease target mRNA levels.哺乳动物的 microRNAs 主要作用是降低靶 mRNA 水平。
Nature. 2010 Aug 12;466(7308):835-40. doi: 10.1038/nature09267.
5
Direct reprogramming of fibroblasts into functional cardiomyocytes by defined factors.通过定义因子将成纤维细胞直接重编程为功能性心肌细胞。
Cell. 2010 Aug 6;142(3):375-86. doi: 10.1016/j.cell.2010.07.002.
6
MiR-322/424 and -503 are induced during muscle differentiation and promote cell cycle quiescence and differentiation by down-regulation of Cdc25A.miR-322/424 和 -503 在肌肉分化过程中被诱导产生,通过下调 Cdc25A 促进细胞周期静止和分化。
Mol Biol Cell. 2010 Jul 1;21(13):2138-49. doi: 10.1091/mbc.e10-01-0062. Epub 2010 May 12.
7
Genome-wide MyoD binding in skeletal muscle cells: a potential for broad cellular reprogramming.基因组范围内的 MyoD 在骨骼肌细胞中的结合:广泛细胞重编程的潜力。
Dev Cell. 2010 Apr 20;18(4):662-74. doi: 10.1016/j.devcel.2010.02.014.
8
Activation of Cdc6 by MyoD is associated with the expansion of quiescent myogenic satellite cells.MyoD 通过激活 Cdc6 与静止的肌卫星细胞的扩增有关。
J Cell Biol. 2010 Jan 11;188(1):39-48. doi: 10.1083/jcb.200904144. Epub 2010 Jan 4.
9
MicroRNA-206 delays ALS progression and promotes regeneration of neuromuscular synapses in mice.miRNA-206 可延缓肌萎缩侧索硬化症的进展并促进小鼠运动神经元-肌肉突触的再生。
Science. 2009 Dec 11;326(5959):1549-54. doi: 10.1126/science.1181046.
10
Mir-214-dependent regulation of the polycomb protein Ezh2 in skeletal muscle and embryonic stem cells.骨骼肌和胚胎干细胞中mir-214对多梳蛋白Ezh2的依赖性调控
Mol Cell. 2009 Oct 9;36(1):61-74. doi: 10.1016/j.molcel.2009.08.008.

微小 RNA-378 在成肌细胞分化过程中靶向肌生成抑制因子 MyoR。

MicroRNA-378 targets the myogenic repressor MyoR during myoblast differentiation.

机构信息

Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA.

出版信息

J Biol Chem. 2011 Jun 3;286(22):19431-8. doi: 10.1074/jbc.M111.219006. Epub 2011 Apr 6.

DOI:10.1074/jbc.M111.219006
PMID:21471220
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3103322/
Abstract

MicroRNAs play important roles in many cell processes, including the differentiation process in several different lineages. For example, microRNAs can promote differentiation by repressing negative regulators of transcriptional activity. These regulated transcription factors can further up-regulate levels of the microRNA in a feed-forward mechanism. Here we show that MyoD up-regulates miR-378 during myogenic differentiation in C2C12 cells. ChIP and high throughput sequencing analysis shows that MyoD binds in close proximity to the miR-378 gene and causes both transactivation and chromatin remodeling. Overexpression of miR-378 increases the transcriptional activity of MyoD, in part by repressing an antagonist, MyoR. The 3' untranslated region of MyoR contains a direct binding site for miR-378. The presence of this binding site significantly reduces the ability of MyoR to prevent the MyoD-driven transdifferentiation of fibroblasts. MyoR and miR-378 were anticorrelated during cardiotoxin-induced adult muscle regeneration in mice. Taken together, this shows a feed-forward loop where MyoD indirectly down-regulates MyoR via miR-378.

摘要

MicroRNAs 在许多细胞过程中发挥重要作用,包括几个不同谱系的分化过程。例如,microRNAs 可以通过抑制转录活性的负调节剂来促进分化。这些受调控的转录因子可以通过正反馈机制进一步上调 microRNA 的水平。在这里,我们表明 MyoD 在 C2C12 细胞的肌生成分化过程中上调 miR-378。ChIP 和高通量测序分析表明,MyoD 紧密结合在 miR-378 基因附近,并导致转录激活和染色质重塑。miR-378 的过表达增加了 MyoD 的转录活性,部分原因是抑制了一种拮抗剂 MyoR。MyoR 的 3'UTR 包含 miR-378 的直接结合位点。该结合位点的存在显著降低了 MyoR 阻止成纤维细胞的 MyoD 驱动的转分化的能力。在小鼠心脏毒素诱导的成年肌肉再生过程中,MyoR 和 miR-378 呈反相关。总之,这表明了一个正反馈回路,其中 MyoD 通过 miR-378 间接下调 MyoR。