Sato K, Miyagi T
Division of Biochemistry, Miyagi Cancer Center, Japan.
Biochem Biophys Res Commun. 1996 Apr 25;221(3):826-30. doi: 10.1006/bbrc.1996.0681.
We have previously observed that the cytosolic sialidase gene is highly expressed in rat skeletal muscle and that it contains an enhancer/promoter region which is transcriptionally active in rat L6 myogenic cells. Here we present evidence for the involvement of cytosolic sialidase in myoblast differentiation. During L6 myoblast differentiation induced by serum depletion, cytosolic sialidase is increased in activity as well as in terms of mRNA level. Sialidase activity is essentially lacking in untreated myoblasts but appears concomitantly with myotube formation after induction of differentiation. The mRNA becomes able to be detected after 3 days at the time which myogenin mRNA reaches a maximum level. Myotube formation can, in fact, be blocked by the addition of an antisense oligodeoxyribonucleotide complementary to the first 8 codons of the cytosolic sialidase.
我们之前观察到,胞质唾液酸酶基因在大鼠骨骼肌中高度表达,并且它包含一个在大鼠L6成肌细胞中具有转录活性的增强子/启动子区域。在此我们提供证据表明胞质唾液酸酶参与了成肌细胞的分化。在血清饥饿诱导的L6成肌细胞分化过程中,胞质唾液酸酶的活性以及mRNA水平均升高。未处理的成肌细胞基本缺乏唾液酸酶活性,但在诱导分化后随着肌管形成而同时出现。在肌细胞生成素mRNA达到最高水平的第3天能够检测到该mRNA。事实上,添加与胞质唾液酸酶前8个密码子互补的反义寡脱氧核糖核苷酸可阻断肌管形成。