Toyota N
Department of Anatomy and Cell Biology, School of Medicine, Chiba University, Japan.
Int J Dev Biol. 1993 Dec;37(4):531-7.
Expression of cardiac troponin C (C/STnC) and fast skeletal muscle troponin C (FTnC) genes during development was analyzed by in situ hybridization and Northern blot. At Hamburger-Hamilton stage 14, FTnC mRNA was detected in somites. At stage 20, FTnC mRNA was identified in truncus arteriosus. FTnC mRNA was undetectable in embryonic ventricle at the other developmental stages. This suggested that transcription of FTnC mRNA at stage 20 was stage and region-specific. At early stage 10, C/STnC mRNA was detected in truncus arteriosus, ventricle and vitelline veins at the proximal region where right and left veins bifurcate from ventricle. In the proximal region of vitelline vein, C/STnC mRNA was transcribed in both the rostral and caudal walls of the veins. The area of C/STnC gene expression in vitelline vein is wider than those of alpha-cardiac and smooth muscle actin genes (Ruzicka and Schwartz, J. Cell Biol. 107: 2575-2586, 1988). It is suggested that C/STnC plays an important role relating embryonic excitation-contraction-coupling in the wider area including vitelline vein. C/STnC mRNA was identified also in somites, embryonic breast muscle and adult breast muscle. Since C/STnC protein was undetectable in adult breast muscle by immunofluorescence microscopy (Toyota and Shimada, J. Cell Biol. 91: 497-504, 1981), the imbalance of C/STnC mRNA and protein levels suggested the operation of specific mechanisms that separately regulated the accumulation of C/STnC mRNA and protein.
通过原位杂交和Northern印迹分析了心脏肌钙蛋白C(C/STnC)和快骨骼肌肌钙蛋白C(FTnC)基因在发育过程中的表达情况。在Hamburger-Hamilton第14阶段,在体节中检测到FTnC mRNA。在第20阶段,在动脉干中鉴定出FTnC mRNA。在其他发育阶段的胚胎心室中未检测到FTnC mRNA。这表明第20阶段FTnC mRNA的转录具有阶段和区域特异性。在第10阶段早期,在动脉干、心室以及左右静脉从心室分叉处近端区域的卵黄静脉中检测到C/STnC mRNA。在卵黄静脉近端区域,C/STnC mRNA在静脉的头侧和尾侧壁均有转录。卵黄静脉中C/STnC基因表达的区域比α-心脏肌动蛋白和平滑肌肌动蛋白基因的表达区域更宽(Ruzicka和Schwartz,《细胞生物学杂志》107: 2575 - 2586,1988)。这表明C/STnC在包括卵黄静脉在内的更广泛区域的胚胎兴奋 - 收缩偶联中发挥重要作用。在体节、胚胎胸肌和成年胸肌中也鉴定出了C/STnC mRNA。由于通过免疫荧光显微镜在成年胸肌中未检测到C/STnC蛋白(Toyota和Shimada,《细胞生物学杂志》91: 497 - 504,1981),C/STnC mRNA和蛋白水平的失衡表明存在分别调节C/STnC mRNA和蛋白积累的特定机制。