Wuebbles Ryan D, Hanel Meredith L, Jones Peter L
Department of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Dis Model Mech. 2009 May-Jun;2(5-6):267-74. doi: 10.1242/dmm.002261. Epub 2009 Apr 21.
The genetic lesion that is diagnostic for facioscapulohumeral muscular dystrophy (FSHD) results in an epigenetic misregulation of gene expression, which ultimately leads to the disease pathology. FRG1 (FSHD region gene 1) is a leading candidate for a gene whose misexpression might lead to FSHD. Because FSHD pathology is most prominent in the musculature, most research and therapy efforts focus on muscle cells. Previously, using Xenopus development as a model, we showed that altering frg1 expression levels systemically leads to aberrant muscle development, illustrating the potential for aberrant FRG1 levels to disrupt the musculature. However, 50-75% of FSHD patients also exhibit retinal vasculopathy and FSHD muscles have increased levels of vascular- and endothelial-related FRG1 transcripts, illustrating an underlying vascular component to the disease. To date, no FSHD candidate gene has been proposed to affect the vasculature. Here, we focus on a role for FRG1 expression in the vasculature. We found that endogenous frg1 is expressed in both the developing and adult vasculature in Xenopus. Furthermore, expression of FRG1 was found to be essential for the development of the vasculature, as a knockdown of FRG1 resulted in decreased angiogenesis and reduced expression of the angiogenic regulator DAB2. Conversely, tadpoles subjected to frg1 overexpression displayed the pro-angiogenic phenotypes of increased blood vessel branching and dilation of blood vessels, and developed edemas, suggesting that their circulation was disrupted. Thus, the systemic upregulation of the FRG1 protein shows the potential for acquiring a disrupted vascular phenotype, providing the first link between a FSHD candidate gene and the vascular component of FSHD pathology. Overall, in conjunction with our previous analysis, we show that FRG1 overexpression is capable of disrupting both the musculature and vasculature, recapitulating the two most prominent features of FSHD.
对面肩肱型肌营养不良症(FSHD)具有诊断意义的基因损伤会导致基因表达的表观遗传失调,最终引发疾病病理变化。FRG1(FSHD区域基因1)是一个主要候选基因,其表达失调可能导致FSHD。由于FSHD病理变化在肌肉组织中最为显著,大多数研究和治疗工作都集中在肌肉细胞上。此前,我们以非洲爪蟾发育为模型,表明系统性改变frg1表达水平会导致异常的肌肉发育,这说明FRG1水平异常有破坏肌肉组织的可能性。然而,50 - 75%的FSHD患者还表现出视网膜血管病变,且FSHD肌肉中与血管和内皮相关的FRG1转录本水平升高,这说明该疾病存在潜在的血管成分。迄今为止,尚无FSHD候选基因被认为会影响血管系统。在此,我们聚焦于FRG1在血管系统中的作用。我们发现非洲爪蟾发育中和成年后的血管系统中均有内源性frg1表达。此外,发现FRG1的表达对血管系统发育至关重要,因为敲低FRG1会导致血管生成减少以及血管生成调节因子DAB2的表达降低。相反,过表达frg1的蝌蚪表现出血管分支增加和血管扩张等促血管生成表型,并出现水肿,这表明它们的循环系统受到了干扰。因此,FRG1蛋白的系统性上调显示出出现血管表型破坏的可能性,这为FSHD候选基因与FSHD病理的血管成分之间提供了首个联系。总体而言,结合我们之前的分析,我们表明FRG1过表达能够破坏肌肉组织和血管系统,重现了FSHD两个最突出的特征。