Suppr超能文献

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.

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。

相似文献

1
Characterization of the DNA-binding properties of the Mohawk homeobox transcription factor.
J Biol Chem. 2012 Oct 12;287(42):35351-35359. doi: 10.1074/jbc.M112.399386. Epub 2012 Aug 24.
3
The Mohawk homeobox gene is a critical regulator of tendon differentiation.
Proc Natl Acad Sci U S A. 2010 Jun 8;107(23):10538-42. doi: 10.1073/pnas.1000525107. Epub 2010 May 24.
4
Gtf2ird1-Dependent Mohawk Expression Regulates Mechanosensing Properties of the Tendon.
Mol Cell Biol. 2016 Mar 31;36(8):1297-309. doi: 10.1128/MCB.00950-15. Print 2016 Apr.
5
The homeobox transcription factor Irxl1 negatively regulates MyoD expression and myoblast differentiation.
FEBS J. 2014 Jul;281(13):2990-3003. doi: 10.1111/febs.12837. Epub 2014 May 27.
6
The atypical homeodomain transcription factor Mohawk controls tendon morphogenesis.
Mol Cell Biol. 2010 Oct;30(20):4797-807. doi: 10.1128/MCB.00207-10. Epub 2010 Aug 9.
9
The Mohawk homeobox transcription factor regulates the differentiation of tendons and volar plates.
J Orthop Sci. 2014 Jan;19(1):172-80. doi: 10.1007/s00776-013-0485-z. Epub 2013 Oct 29.
10
The transcription factor mohawk homeobox regulates homeostasis of the periodontal ligament.
Development. 2017 Jan 15;144(2):313-320. doi: 10.1242/dev.135798. Epub 2016 Dec 19.

引用本文的文献

1
IRX3 controls a SUMOylation-dependent differentiation switch in adipocyte precursor cells.
Nat Commun. 2025 Aug 6;16(1):7248. doi: 10.1038/s41467-025-62361-1.
2
Transcription factor Mohawk regulates tendon/ligament development: A narrative review.
Medicine (Baltimore). 2025 Jul 25;104(30):e43044. doi: 10.1097/MD.0000000000043044.
3
Characterization of PRDM9 Multifunctionality in Yak Testes Through Protein Interaction Mapping.
Int J Mol Sci. 2025 Feb 8;26(4):1420. doi: 10.3390/ijms26041420.
4
Experimental approaches to investigate biophysical interactions between homeodomain transcription factors and DNA.
Biochim Biophys Acta Gene Regul Mech. 2025 Mar;1868(1):195074. doi: 10.1016/j.bbagrm.2024.195074. Epub 2024 Dec 5.
8
External stimulation: A potential therapeutic strategy for tendon-bone healing.
Front Bioeng Biotechnol. 2023 Mar 31;11:1150290. doi: 10.3389/fbioe.2023.1150290. eCollection 2023.
10
Hemocyte Clusters Defined by scRNA-Seq in : Analysis of Predicted Marker Genes and Implications for Potential Functional Roles.
Front Immunol. 2022 Feb 25;13:852702. doi: 10.3389/fimmu.2022.852702. eCollection 2022.

本文引用的文献

1
Negative feedback and physical limits of genes.
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.
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.
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.
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.
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.
J Bacteriol. 2009 Jul;191(14):4487-91. doi: 10.1128/JB.00056-09. Epub 2009 May 8.
7
Transcriptional autoregulation in development.
Curr Biol. 2009 Mar 24;19(6):R241-6. doi: 10.1016/j.cub.2009.01.015.
10
Variation in homeodomain DNA binding revealed by high-resolution analysis of sequence preferences.
Cell. 2008 Jun 27;133(7):1266-76. doi: 10.1016/j.cell.2008.05.024.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验