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本文引用的文献

1
Negative feedback and physical limits of genes.负反馈和基因的物理极限。
J Theor Biol. 2011 Sep 7;284(1):82-91. doi: 10.1016/j.jtbi.2011.06.021. Epub 2011 Jun 25.
2
Concerted regulation of myofiber-specific gene expression and muscle performance by the transcriptional repressor Sox6.转录抑制因子 Sox6 对肌纤维特异性基因表达和肌肉性能的协同调节。
Proc Natl Acad Sci U S A. 2011 Jun 21;108(25):10196-201. doi: 10.1073/pnas.1107413108. Epub 2011 Jun 1.
3
Down-regulation of Runx1 expression by TCR signal involves an autoregulatory mechanism and contributes to IL-2 production.TCR 信号下调 Runx1 的表达涉及一个自身调控机制,并有助于 IL-2 的产生。
J Biol Chem. 2011 Apr 1;286(13):11110-8. doi: 10.1074/jbc.M110.166694. Epub 2011 Feb 3.
4
The atypical homeodomain transcription factor Mohawk controls tendon morphogenesis.非典型同源结构域转录因子 Mohawk 控制肌腱形态发生。
Mol Cell Biol. 2010 Oct;30(20):4797-807. doi: 10.1128/MCB.00207-10. Epub 2010 Aug 9.
5
The Mohawk homeobox gene is a critical regulator of tendon differentiation.莫霍克同源盒基因是肌腱分化的关键调节因子。
Proc Natl Acad Sci U S A. 2010 Jun 8;107(23):10538-42. doi: 10.1073/pnas.1000525107. Epub 2010 May 24.
6
Dominant negative autoregulation limits steady-state repression levels in gene networks.显性负向自动调节限制了基因网络中的稳态抑制水平。
J Bacteriol. 2009 Jul;191(14):4487-91. doi: 10.1128/JB.00056-09. Epub 2009 May 8.
7
Transcriptional autoregulation in development.发育过程中的转录自调控
Curr Biol. 2009 Mar 24;19(6):R241-6. doi: 10.1016/j.cub.2009.01.015.
8
The homeobox gene Mohawk represses transcription by recruiting the sin3A/HDAC co-repressor complex.同源异型盒基因莫霍克通过招募sin3A/HDAC共抑制复合物来抑制转录。
Dev Dyn. 2009 Mar;238(3):572-80. doi: 10.1002/dvdy.21873.
9
Analysis of homeodomain specificities allows the family-wide prediction of preferred recognition sites.对同源结构域特异性的分析能够实现全家族范围内对偏好识别位点的预测。
Cell. 2008 Jun 27;133(7):1277-89. doi: 10.1016/j.cell.2008.05.023.
10
Variation in homeodomain DNA binding revealed by high-resolution analysis of sequence preferences.通过对序列偏好的高分辨率分析揭示的同源域DNA结合变异。
Cell. 2008 Jun 27;133(7):1266-76. doi: 10.1016/j.cell.2008.05.024.

莫霍克同源盒转录因子的 DNA 结合特性分析。

Characterization of the DNA-binding properties of the Mohawk homeobox transcription factor.

机构信息

School of Life Sciences, Biodesign Institute, Arizona State University, Tempe, Arizona 85287-4501; Molecular and Cellular Biology Graduate Program, Biodesign Institute, Arizona State University, Tempe, Arizona 85287-4501.

Program in Gene Function and Expression, University of Massachusetts Medical School, Worcester, Massachusetts 01605; Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts 01605.

出版信息

J Biol Chem. 2012 Oct 12;287(42):35351-35359. doi: 10.1074/jbc.M112.399386. Epub 2012 Aug 24.

DOI:10.1074/jbc.M112.399386
PMID:22923612
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3471766/
Abstract

The homeobox transcription factor Mohawk (Mkx) is a potent transcriptional repressor expressed in the embryonic precursors of skeletal muscle, cartilage, and bone. MKX has recently been shown to be a critical regulator of musculoskeletal tissue differentiation and gene expression; however, the genetic pathways through which MKX functions and its DNA-binding properties are currently unknown. Using a modified bacterial one-hybrid site selection assay, we determined the core DNA-recognition motif of the mouse monomeric Mkx homeodomain to be A-C-A. Using cell-based assays, we have identified a minimal Mkx-responsive element (MRE) located within the Mkx promoter, which is composed of a highly conserved inverted repeat of the core Mkx recognition motif. Using the minimal MRE sequence, we have further identified conserved MREs within the locus of Sox6, a transcription factor that represses slow fiber gene expression during skeletal muscle differentiation. Real-time PCR and immunostaining of in vitro differentiated muscle satellite cells isolated from Mkx-null mice revealed an increase in the expression of Sox6 and down-regulation of slow fiber structural genes. Together, these data identify the unique DNA-recognition properties of MKX and reveal a novel role for Mkx in promoting slow fiber type specification during skeletal muscle differentiation.

摘要

同源盒转录因子 Mohawk(Mkx)是一种在骨骼肌、软骨和骨骼的胚胎前体细胞中表达的强效转录抑制剂。MKX 最近被证明是肌肉骨骼组织分化和基因表达的关键调节因子;然而,MKX 发挥作用的遗传途径及其 DNA 结合特性目前尚不清楚。我们使用改良的细菌单杂交位点选择测定法,确定了小鼠单体 Mkx 同源域的核心 DNA 识别基序为 A-C-A。通过细胞测定法,我们在 Mkx 启动子内鉴定出一个最小的 Mkx 反应元件(MRE),该元件由核心 Mkx 识别基序的高度保守反向重复组成。使用最小的 MRE 序列,我们在 Sox6 的基因座内进一步鉴定出保守的 MRE,Sox6 是一种转录因子,在骨骼肌分化过程中抑制慢肌纤维基因的表达。从 Mkx 缺失小鼠分离的体外分化的肌肉卫星细胞的实时 PCR 和免疫染色显示 Sox6 的表达增加,慢肌纤维结构基因的下调。这些数据共同确定了 MKX 的独特 DNA 识别特性,并揭示了 Mkx 在促进骨骼肌分化过程中慢肌纤维类型特化中的新作用。