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本文引用的文献

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Distinct Activities of Myf5 and MyoD Indicate Separate Roles in Skeletal Muscle Lineage Specification and Differentiation.Myf5和MyoD的不同活性表明它们在骨骼肌谱系特化和分化中具有不同作用。
Dev Cell. 2016 Feb 22;36(4):375-85. doi: 10.1016/j.devcel.2016.01.021.
2
Wnt signaling in bone and muscle.骨骼与肌肉中的Wnt信号传导
Bone. 2015 Nov;80:60-66. doi: 10.1016/j.bone.2015.02.009.
3
Gene regulatory networks and transcriptional mechanisms that control myogenesis.控制肌发生的基因调控网络和转录机制。
Dev Cell. 2014 Feb 10;28(3):225-38. doi: 10.1016/j.devcel.2013.12.020.
4
eRNAs promote transcription by establishing chromatin accessibility at defined genomic loci.增强子 RNA 通过在特定基因组位置建立染色质可及性来促进转录。
Mol Cell. 2013 Sep 12;51(5):606-17. doi: 10.1016/j.molcel.2013.07.022. Epub 2013 Aug 29.
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Hedgehog signaling regulates MyoD expression and activity.Hedgehog 信号通路调控 MyoD 的表达和活性。
J Biol Chem. 2013 Feb 8;288(6):4389-404. doi: 10.1074/jbc.M112.400184. Epub 2012 Dec 24.
6
Sonic hedgehog acts cell-autonomously on muscle precursor cells to generate limb muscle diversity. sonic hedgehog ( SHH ) 通过对肌肉前体细胞的自主作用产生肢体肌肉多样性。
Genes Dev. 2012 Sep 15;26(18):2103-17. doi: 10.1101/gad.187807.112.
7
Wnt signaling in myogenesis.Wnt 信号在成肌中的作用。
Trends Cell Biol. 2012 Nov;22(11):602-9. doi: 10.1016/j.tcb.2012.07.008. Epub 2012 Aug 31.
8
Carm1 regulates Pax7 transcriptional activity through MLL1/2 recruitment during asymmetric satellite stem cell divisions.Carm1 通过募集 MLL1/2 来调节 Pax7 的转录活性,从而在不对称卫星干细胞分裂过程中发挥作用。
Cell Stem Cell. 2012 Sep 7;11(3):333-45. doi: 10.1016/j.stem.2012.07.001. Epub 2012 Aug 2.
9
Comparative expression profiling identifies differential roles for Myogenin and p38α MAPK signaling in myogenesis.比较表达谱分析确定了 Myogenin 和 p38α MAPK 信号在成肌分化中的不同作用。
J Mol Cell Biol. 2012 Dec;4(6):386-97. doi: 10.1093/jmcb/mjs045. Epub 2012 Jul 30.
10
Snail regulates MyoD binding-site occupancy to direct enhancer switching and differentiation-specific transcription in myogenesis.蜗牛调节 MyoD 结合位点的占据,以指导肌肉发生中的增强子转换和分化特异性转录。
Mol Cell. 2012 Aug 10;47(3):457-68. doi: 10.1016/j.molcel.2012.05.046. Epub 2012 Jul 5.

肌生成调节因子,肌肉发育、细胞特性和再生的决定因素。

The myogenic regulatory factors, determinants of muscle development, cell identity and regeneration.

机构信息

The Sprott Centre for Stem Cell Research, Regenerative Medicine Program, Ottawa Hospital Research Institute, 501 Smyth Road, Ottawa, ON, K1H 8L6, Canada; Departments of Medicine and Cellular and Molecular Medicine, University of Ottawa, 451 Smyth Road, Ottawa, ON, K1H 8M5, Canada.

The Sprott Centre for Stem Cell Research, Regenerative Medicine Program, Ottawa Hospital Research Institute, 501 Smyth Road, Ottawa, ON, K1H 8L6, Canada; Departments of Medicine and Cellular and Molecular Medicine, University of Ottawa, 451 Smyth Road, Ottawa, ON, K1H 8M5, Canada.

出版信息

Semin Cell Dev Biol. 2017 Dec;72:10-18. doi: 10.1016/j.semcdb.2017.11.010. Epub 2017 Nov 15.

DOI:10.1016/j.semcdb.2017.11.010
PMID:29127045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5723221/
Abstract

The Myogenic Regulatory Factors (MRFs) Myf5, MyoD, myogenin and MRF4 are members of the basic helix-loop-helix family of transcription factors that control the determination and differentiation of skeletal muscle cells during embryogenesis and postnatal myogenesis. The dynamics of their temporal and spatial expression as well as their biochemical properties have allowed the identification of a precise and hierarchical relationship between the four MRFs. This relationship establishes the myogenic lineage as well as the maintenance of the terminal myogenic phenotype. The application of genome-wide technologies has provided important new information as to how the MRFs function to activate muscle gene expression. Application of combined functional genomics technologies along with single cell lineage tracing strategies will allow a deeper understanding of the mechanisms mediating myogenic determination, cell differentiation and muscle regeneration.

摘要

肌生成调节因子(MRFs)Myf5、MyoD、myogenin 和 MRF4 是基本螺旋-环-螺旋家族转录因子的成员,它们在胚胎发生和出生后肌发生过程中控制骨骼肌细胞的决定和分化。它们的时空表达的动态以及它们的生化特性允许在四个 MRF 之间确定一个精确的和分层的关系。这种关系建立了肌生成谱系以及终末肌表型的维持。全基因组技术的应用提供了关于 MRFs 如何激活肌肉基因表达的重要新信息。结合功能基因组学技术和单细胞谱系追踪策略的应用将允许更深入地了解介导肌生成决定、细胞分化和肌肉再生的机制。