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本文引用的文献

1
Implication of a multisubunit Ets-related transcription factor in synaptic expression of the nicotinic acetylcholine receptor.一种多亚基Ets相关转录因子在烟碱型乙酰胆碱受体突触表达中的作用
EMBO J. 1998 Jun 1;17(11):3078-90. doi: 10.1093/emboj/17.11.3078.
2
Sp1 cooperates with the ets transcription factor, GABP, to activate the CD18 (beta2 leukocyte integrin) promoter.Sp1与ets转录因子GABP协同作用,以激活CD18(β2白细胞整合素)启动子。
J Biol Chem. 1998 May 22;273(21):13097-103. doi: 10.1074/jbc.273.21.13097.
3
Identification of a neuregulin and protein-tyrosine phosphatase response element in the nicotinic acetylcholine receptor epsilon subunit gene: regulatory role of an Rts transcription factor.在烟碱型乙酰胆碱受体ε亚基基因中鉴定神经调节蛋白和蛋白酪氨酸磷酸酶反应元件:一种Rts转录因子的调节作用。
Proc Natl Acad Sci U S A. 1998 Feb 3;95(3):1289-94. doi: 10.1073/pnas.95.3.1289.
4
Muscle and neural isoforms of agrin increase utrophin expression in cultured myotubes via a transcriptional regulatory mechanism.聚集蛋白的肌肉和神经亚型通过转录调控机制增加培养的肌管中抗肌萎缩蛋白的表达。
J Biol Chem. 1998 Jan 9;273(2):736-43. doi: 10.1074/jbc.273.2.736.
5
GABP cooperates with c-Myb and C/EBP to activate the neutrophil elastase promoter.GA结合蛋白与c-Myb和C/EBP协同激活中性粒细胞弹性蛋白酶启动子。
Blood. 1997 Jun 15;89(12):4546-54.
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Local transcriptional control of utrophin expression at the neuromuscular synapse.神经肌肉突触处肌动蛋白相关蛋白表达的局部转录调控。
J Biol Chem. 1997 Mar 28;272(13):8117-20. doi: 10.1074/jbc.272.13.8117.
7
ARIA: a neuromuscular junction neuregulin.ARIA:一种神经肌肉接头神经调节蛋白。
Annu Rev Neurosci. 1997;20:429-58. doi: 10.1146/annurev.neuro.20.1.429.
8
Dystrophin-associated proteins and the muscular dystrophies.肌营养不良蛋白相关蛋白与肌营养不良症
Annu Rev Med. 1997;48:457-66. doi: 10.1146/annurev.med.48.1.457.
9
Utrophin muscles in on the action.肌营养不良蛋白相关蛋白在发挥作用。
Nat Med. 1997 Jan;3(1):22-3. doi: 10.1038/nm0197-22.
10
Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene.使用截短的抗肌萎缩蛋白转基因改善mdx小鼠的营养不良表型。
Nature. 1996 Nov 28;384(6607):349-53. doi: 10.1038/384349a0.

神经调节蛋白通过与ETS相关的转录因子复合物GA结合蛋白α/β激活肌萎缩蛋白启动子。

Activation of utrophin promoter by heregulin via the ets-related transcription factor complex GA-binding protein alpha/beta.

作者信息

Khurana T S, Rosmarin A G, Shang J, Krag T O, Das S, Gammeltoft S

机构信息

Department of Clinical Biochemistry, University of Copenhagen Medical School, The Glostrup Hospital, Glostrup DK 2600, Denmark.

出版信息

Mol Biol Cell. 1999 Jun;10(6):2075-86. doi: 10.1091/mbc.10.6.2075.

DOI:10.1091/mbc.10.6.2075
PMID:10359616
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC25417/
Abstract

Utrophin/dystrophin-related protein is the autosomal homologue of the chromosome X-encoded dystrophin protein. In adult skeletal muscle, utrophin is highly enriched at the neuromuscular junction. However, the molecular mechanisms underlying regulation of utrophin gene expression are yet to be defined. Here we demonstrate that the growth factor heregulin increases de novo utrophin transcription in muscle cell cultures. Using mutant reporter constructs of the utrophin promoter, we define the N-box region of the promoter as critical for heregulin-mediated activation. Using this region of the utrophin promoter for DNA affinity purification, immunoblots, in vitro kinase assays, electrophoretic mobility shift assays, and in vitro expression in cultured muscle cells, we demonstrate that ets-related GA-binding protein alpha/beta transcription factors are activators of the utrophin promoter. Taken together, these results suggest that the GA-binding protein alpha/beta complex of transcription factors binds and activates the utrophin promoter in response to heregulin-activated extracellular signal-regulated kinase in muscle cell cultures. These findings suggest methods for achieving utrophin up-regulation in Duchenne's muscular dystrophy as well as mechanisms by which neurite-derived growth factors such as heregulin may influence the regulation of utrophin gene expression and subsequent enrichment at the neuromuscular junction of skeletal muscle.

摘要

肌养蛋白/肌营养不良蛋白相关蛋白是X染色体编码的肌营养不良蛋白的常染色体同源物。在成年骨骼肌中,肌养蛋白在神经肌肉接头处高度富集。然而,肌养蛋白基因表达调控的分子机制尚未明确。在此,我们证明生长因子神经调节蛋白可增加肌肉细胞培养物中肌养蛋白的从头转录。利用肌养蛋白启动子的突变报告基因构建体,我们将启动子的N盒区域定义为神经调节蛋白介导的激活所必需的区域。利用肌养蛋白启动子的这一区域进行DNA亲和纯化、免疫印迹、体外激酶测定、电泳迁移率变动分析以及在培养的肌肉细胞中的体外表达,我们证明ets相关GA结合蛋白α/β转录因子是肌养蛋白启动子的激活剂。综上所述,这些结果表明,在肌肉细胞培养物中,转录因子的GA结合蛋白α/β复合物响应神经调节蛋白激活的细胞外信号调节激酶,结合并激活肌养蛋白启动子。这些发现提示了在杜氏肌营养不良症中实现肌养蛋白上调的方法,以及神经调节蛋白等神经突衍生生长因子可能影响肌养蛋白基因表达调控及随后在骨骼肌神经肌肉接头处富集的机制。