Li L, Miano J M, Cserjesi P, Olson E N
Department of Biochemistry and Molecular Biology, University of Texas M.D. Anderson Cancer Center, Houston 75235-9148, USA.
Circ Res. 1996 Feb;78(2):188-95. doi: 10.1161/01.res.78.2.188.
SM22 alpha is a calponin-related protein that is expressed specifically in adult smooth muscle. To begin to define the mechanisms that regulate the establishment of the smooth muscle lineage, we analyzed the expression pattern of the SM22 alpha gene during mouse embryogenesis. In situ hybridization demonstrated that SM22 alpha transcripts were first expressed in vascular smooth muscle cells at about embryonic day (E) 9.5 and thereafter continued to be expressed in all smooth muscle cells into adulthood. In contrast to its smooth muscle specificity in adult tissues, SM22 alpha was expressed transiently in the heart between E8.0 and E12.5 and in skeletal muscle cells in the myotomal compartment of the somites between E9.5 and E12.5. The expression of SM22 alpha in smooth muscle cells, as well as early cardiac and skeletal muscle cells, suggests that there may be commonalities between the regulatory programs that direct muscle-specific gene expression in these three myogenic cell types.
SM22α是一种与钙调蛋白相关的蛋白质,在成年平滑肌中特异性表达。为了开始确定调节平滑肌谱系建立的机制,我们分析了小鼠胚胎发育过程中SM22α基因的表达模式。原位杂交显示,SM22α转录本在大约胚胎第9.5天首次在血管平滑肌细胞中表达,此后在所有平滑肌细胞中持续表达直至成年。与其在成年组织中的平滑肌特异性不同,SM22α在胚胎第8.0天至12.5天期间在心脏中短暂表达,在胚胎第9.5天至12.5天期间在体节的肌节区的骨骼肌细胞中短暂表达。SM22α在平滑肌细胞以及早期心肌和骨骼肌细胞中的表达表明,在指导这三种肌源性细胞类型中肌肉特异性基因表达的调控程序之间可能存在共性。