Gard D L, Lazarides E
Cell. 1980 Jan;19(1):263-75. doi: 10.1016/0092-8674(80)90408-0.
Electrophoretic and autoradiographic analyses of the incorporation of 35S--methionine into newly synthesized proteins during myogenesis reveal that presumptive chicken myoblasts synthesize primarily one intermediate filament protein: vimentin. Desmin synthesis is initiated at the onset of fusion. Synthesis rates of both filament subunits increase during the first three days in culture, relative to the total protein synthesis rate. The observed increase in the rate of desmin synthesis (at least 10 fold) is significantly greater than that observed for vimentin, and is responsible for a net increase in the cellular desmin content relative to vimentin. Both filament subunits continue to be synthesized through at least 20 days in culture. Immunofluorescent staining using desmin- and vimentin-specific antisera supports the conclusion that desmin is synthesized only in fusing or multinucleate cells. These results indicate that the synthesis of the two filament subunits is not coordinately regulated during myogenesis. The distributions of desmin and vimentin in multinucleate chicken myotubes are indistinguishable, as determined by double immunofluorescence techniques. In early myotubes, both proteins are found in an intricate network of free cytoplasmic filaments. Later in myogenesis, several days after the appearance of alpha--actinin-containing Z line striations, both filament proteins become associated with the Z lines of newly assembled myofibrils, with a corresponding decrease in the number of cytoplasmic filaments. This transition corresponds to the time when the alpha--actinin-containing Z lines become aligned laterally. These data suggest that the two intermediate filament systems, desmin and vimentin, have an important role in the lateral organization and registration of myofibrils and that the synthesis of desmin and assembly of desmin-containing intermediate filaments during myogenesis is directly related to these functions. These results also indicate that the Z disc is assembled in at least two distinct steps during myogenesis.
在肌生成过程中,对新合成蛋白质中35S-甲硫氨酸掺入情况进行的电泳和放射自显影分析表明,推测的鸡成肌细胞主要合成一种中间丝蛋白:波形蛋白。结蛋白的合成在融合开始时启动。相对于总蛋白质合成速率,在培养的头三天中,两种丝亚基的合成速率均增加。观察到的结蛋白合成速率增加(至少10倍)明显大于波形蛋白,并且导致细胞内结蛋白含量相对于波形蛋白的净增加。两种丝亚基在培养至少20天的时间里持续合成。使用结蛋白和波形蛋白特异性抗血清进行的免疫荧光染色支持以下结论:结蛋白仅在正在融合或多核的细胞中合成。这些结果表明,在肌生成过程中,两种丝亚基的合成并非协同调节。通过双重免疫荧光技术确定,结蛋白和波形蛋白在多核鸡肌管中的分布无法区分。在早期肌管中,两种蛋白质都存在于复杂的游离细胞质丝网络中。在肌生成后期,即在含α-辅肌动蛋白的Z线条纹出现几天后,两种丝蛋白都与新组装肌原纤维的Z线相关联,同时细胞质丝的数量相应减少。这种转变与含α-辅肌动蛋白的Z线横向排列的时间相对应。这些数据表明,结蛋白和波形蛋白这两种中间丝系统在肌原纤维的横向组织和对齐中具有重要作用,并表明在肌生成过程中结蛋白的合成以及含结蛋白的中间丝的组装与这些功能直接相关。这些结果还表明,在肌生成过程中,Z盘至少通过两个不同步骤组装而成。