Kemp T J, Sadusky T J, Saltisi F, Carey N, Moss J, Yang S Y, Sassoon D A, Goldspink G, Coulton G R
Division of Biomedical Sciences, Imperial College of Science, Technology and Medicine, London, SW7 2AZ, United Kingdom.
Genomics. 2000 Jun 15;66(3):229-41. doi: 10.1006/geno.2000.6213.
Mechanically induced hypertrophy of skeletal muscles involves shifts in gene expression leading to increases in the synthesis of specific proteins. Full characterization of the regulation of muscle hypertrophy is a prerequisite for the development of novel therapies aimed at treating muscle wasting (atrophy) in human aging and disease. Using suppression subtractive hybridization, cDNAs corresponding to mRNAs that increase in relative abundance in response to mechanical stretch of mouse skeletal muscles in vivo were identified. A novel 1100-bp transcript was detected exclusively in skeletal muscle. This exhibited a fourfold increase in expression after 7 days of stretch. The transcript had an open reading frame of 328 amino acids encoding an ATP/GTP binding domain, a nuclear localization signal, two PEST protein-destabilization motifs, and a 132-amino-acid ankyrin-repeat region. We have named this gene ankyrin-repeat domain 2 (stretch-responsive muscle) (Ankrd2). We hypothesize that Ankrd2 plays an important role in skeletal muscle hypertrophy.
机械诱导的骨骼肌肥大涉及基因表达的改变,从而导致特定蛋白质合成增加。全面表征肌肉肥大的调节机制是开发旨在治疗人类衰老和疾病中肌肉萎缩的新疗法的先决条件。利用抑制性消减杂交技术,鉴定出了与在体内对小鼠骨骼肌进行机械拉伸时相对丰度增加的mRNA相对应的cDNA。一种新的1100bp转录本仅在骨骼肌中被检测到。在拉伸7天后,其表达增加了四倍。该转录本有一个328个氨基酸的开放阅读框,编码一个ATP/GTP结合结构域、一个核定位信号、两个PEST蛋白不稳定基序和一个132个氨基酸的锚蛋白重复区域。我们将这个基因命名为锚蛋白重复结构域2(拉伸反应性肌肉)(Ankrd2)。我们推测Ankrd2在骨骼肌肥大中起重要作用。