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Lysophosphatidic acid 2 receptor-mediated supramolecular complex formation regulates its antiapoptotic effect.溶血磷脂酸2受体介导的超分子复合物形成调节其抗凋亡作用。
J Biol Chem. 2009 May 22;284(21):14558-71. doi: 10.1074/jbc.M900185200. Epub 2009 Mar 17.
2
Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.由FHL1基因突变引起的还原体肌病的临床、组织学和遗传学特征
Brain. 2009 Feb;132(Pt 2):452-64. doi: 10.1093/brain/awn325. Epub 2009 Jan 29.
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Novel FHL1 mutations in fatal and benign reducing body myopathy.致死性和良性还原小体性肌病中的新型FHL1突变
Neurology. 2009 Jan 27;72(4):375-6. doi: 10.1212/01.wnl.0000341311.84347.a0.
4
Identification of FHL1 as a regulator of skeletal muscle mass: implications for human myopathy.鉴定FHL1作为骨骼肌质量的调节因子:对人类肌病的影响。
J Cell Biol. 2008 Dec 15;183(6):1033-48. doi: 10.1083/jcb.200804077.
5
Rigid spine syndrome caused by a novel mutation in four-and-a-half LIM domain 1 gene (FHL1).由四半LIM结构域1基因(FHL1)的新型突变引起的僵硬脊柱综合征。
Neuromuscul Disord. 2008 Dec;18(12):959-61. doi: 10.1016/j.nmd.2008.09.012. Epub 2008 Oct 25.
6
KyoT3, an isoform of murine FHL1, associates with the transcription factor RBP-J and represses the RBP-J-mediated transactivation.KyoT3是小鼠FHL1的一种异构体,它与转录因子RBP-J结合并抑制RBP-J介导的反式激活。
Biochim Biophys Acta. 2008 Dec;1779(12):805-10. doi: 10.1016/j.bbagrm.2008.08.001. Epub 2008 Aug 9.
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The genetics of vertebrate myogenesis.脊椎动物肌发生的遗传学
Nat Rev Genet. 2008 Aug;9(8):632-46. doi: 10.1038/nrg2369.
8
Molecular-targeted therapy for Duchenne muscular dystrophy: progress and potential.杜氏肌营养不良症的分子靶向治疗:进展与潜力
Mol Diagn Ther. 2008;12(2):99-108. doi: 10.1007/BF03256275.
9
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy.蛋白质组学鉴定FHL1为人类还原体肌病中发生突变的蛋白质。
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Modulation of age-induced apoptotic signaling and cellular remodeling by exercise and calorie restriction in skeletal muscle.运动和热量限制对骨骼肌中年龄诱导的凋亡信号传导和细胞重塑的调节作用。
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SLIMMER(FHL1B/KyoT3)与促凋亡蛋白Siva-1(CD27BP)相互作用,并延缓骨骼肌成肌细胞凋亡。

SLIMMER (FHL1B/KyoT3) interacts with the proapoptotic protein Siva-1 (CD27BP) and delays skeletal myoblast apoptosis.

作者信息

Cottle Denny L, McGrath Meagan J, Wilding Brendan R, Cowling Belinda S, Kane Jordan M, D'Arcy Colleen E, Holdsworth Melissa, Hatzinisiriou Irene, Prescott Mark, Brown Susan, Mitchell Christina A

机构信息

Department of Biochemistry and Molecular Biology, Monash University, Clayton, 3800 Victoria, Australia.

出版信息

J Biol Chem. 2009 Sep 25;284(39):26964-77. doi: 10.1074/jbc.M109.036293. Epub 2009 Jul 29.

DOI:10.1074/jbc.M109.036293
PMID:19643733
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2786031/
Abstract

The fhl1 gene encoding four-and-a-half LIM protein-1 (FHL1) and its spliced isoform, SLIMMER, is mutated in reducing body myopathy, X-linked myopathy with postural muscle atrophy, scapuloperoneal myopathy, and rigid spine syndrome. In this study we have identified a novel function for SLIMMER in delaying skeletal muscle apoptosis via an interaction with the proapoptotic protein Siva-1. Siva-1 was identified as a SLIMMER-specific-interacting protein using yeast two-hybrid screening, direct-binding studies, and glutathione S-transferase pulldown analysis of murine skeletal muscle lysates. In C2C12 skeletal myoblasts, SLIMMER and Siva co-localized in the nucleus; however, both proteins exhibited redistribution to the cytoplasm following the differentiation of mononucleated myoblasts to multinucleated myotubes. In sections of mature skeletal muscle from wild type mice, SLIMMER and Siva-1 co-localized at the Z-line. SLIMMER and Siva-1 were also enriched in Pax-7-positive satellite cells, muscle stem cells that facilitate repair and regeneration. Significantly, SLIMMER delayed Siva-1-dependent apoptosis in C2C12 myoblasts. In skeletal muscle sections from the mdx mouse model of Duchenne muscular dystrophy, SLIMMER and Siva-1 co-localized in the nucleus of apoptotic myofibers. Therefore, SLIMMER may protect skeletal muscle from apoptosis.

摘要

编码四又二分之一LIM蛋白-1(FHL1)及其剪接异构体SLIMMER的fhl1基因,在减少性身体肌病、X连锁姿势性肌肉萎缩性肌病、肩胛腓骨肌病和僵硬脊柱综合征中发生突变。在本研究中,我们通过与促凋亡蛋白Siva-1相互作用,确定了SLIMMER在延迟骨骼肌凋亡方面的新功能。利用酵母双杂交筛选、直接结合研究以及对小鼠骨骼肌裂解物的谷胱甘肽S-转移酶下拉分析,将Siva-1鉴定为一种SLIMMER特异性相互作用蛋白。在C2C12骨骼肌成肌细胞中,SLIMMER和Siva共定位于细胞核;然而,在单核成肌细胞分化为多核肌管后,这两种蛋白均重新分布到细胞质中。在野生型小鼠成熟骨骼肌切片中,SLIMMER和Siva-1共定位于Z线。SLIMMER和Siva-1在促进修复和再生的肌肉干细胞Pax-7阳性卫星细胞中也有富集。值得注意的是,SLIMMER延迟了C2C12成肌细胞中Siva-1依赖性凋亡。在杜兴肌营养不良症的mdx小鼠模型的骨骼肌切片中,SLIMMER和Siva-1共定位于凋亡肌纤维的细胞核中。因此,SLIMMER可能保护骨骼肌免于凋亡。