Sutherland C J, Esser K A, Elsom V L, Gordon M L, Hardeman E C
Muscle Development Unit, Children's Medical Research Institute, Wentworthville, N.S.W., Australia.
Dev Dyn. 1993 Jan;196(1):25-36. doi: 10.1002/aja.1001960104.
The functional diversity of skeletal muscle is largely determined by the combinations of contractile protein isoforms that are expressed in different fibers. Just how the developmental expression of this large array of genes is regulated to give functional phenotypes is thus of great interest. In the present study, we performed a comprehensive analysis of contractile protein isoform mRNA profiles in skeletal muscle systems representing each generation of fiber formed: primary, secondary, and regenerating fibers. We find that in each system examined there is a common pattern of isoform gene expression during early differentiation for 5 of the 6 gene families we have investigated: myosin light chain (MLC)1, MLC2, tropomyosin, troponin (Tn)C, and TnI. We suggest that the common isoform patterns observed together represent a genetic program of skeletal muscle differentiation that is independent of the mature fiber phenotype and is found in all newly formed myotubes. Within each of these contractile protein gene families the program is independent of the isoforms of myosin heavy chain (MHC) expressed. The maintenance of such a program may reflect a specific requirement of the initial differentiation process.
骨骼肌的功能多样性很大程度上由不同纤维中表达的收缩蛋白异构体组合所决定。因此,如何调控这一大类基因的发育表达以产生功能表型就成为了一个备受关注的问题。在本研究中,我们对骨骼肌系统中收缩蛋白异构体的mRNA谱进行了全面分析,这些骨骼肌系统代表了形成的每一代纤维:初级纤维、次级纤维和再生纤维。我们发现,在所研究的6个基因家族中的5个,即肌球蛋白轻链(MLC)1、MLC2、原肌球蛋白、肌钙蛋白(Tn)C和TnI,在每个被检测的系统中,早期分化过程中异构体基因表达都存在一种共同模式。我们认为,共同观察到的这些异构体模式代表了骨骼肌分化的一个遗传程序,它独立于成熟纤维表型,并且在所有新形成的肌管中都能发现。在这些收缩蛋白基因家族中的每一个家族内,该程序都独立于所表达的肌球蛋白重链(MHC)的异构体。维持这样一个程序可能反映了初始分化过程的特定要求。