CDNA CLONING AND MESSENGER-RNA EXPRESSION OF CALPONIN AND SM22 IN RAT AORTA SMOOTH-MUSCLE CELLS

被引:70
作者
NISHIDA, W [1 ]
KITAMI, Y [1 ]
HIWADA, K [1 ]
机构
[1] EHIME UNIV,SCH MED,DEPT INTERNAL MED 2,SHIGENOBU,EHIME 79102,JAPAN
关键词
THIN FILAMENT; ACTOMYOSIN REGULATION; CALDESMON; CDNA CLONING; MESSENGER RNA QUANTIFICATION; DEVELOPMENT; WISTAR KYOTO RAT; SPONTANEOUSLY HYPERTENSIVE RAT;
D O I
10.1016/0378-1119(93)90435-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We cloned and sequenced cDNAs encoding calponin (Calp) and SM22 (smooth muscle-specific 22-kDa protein) from rat aorta (RaA) smooth muscle (Smu) cells. The 1504-bp calp cDNA contains a single open reading frame (ORF) which encodes 297 amino acids (aa) (M(r) 33 342). The 1186-bp SM22 cDNA contains a single ORF which encodes 201 aa (M(r) 22 601). There were 43% identical aa in a 181-aa overlap between RaA Calp and SM22. Especially for the C-terminal region of SM22 and for the first repeat motif of Calp, 70% identity was observed. Northern blot analysis revealed that the calp and SM22 mRNAs were expressed in RaA Smu, but not in rat cardiac and skeletal muscles. SM22 mRNA was much more abundant than calp mRNA in RaA (3- to 4-fold). The expression levels of the calp and SM22 mRNAs in RaA showed a significant increase for 5 to 15 week old rats (1.5- to 3-fold) with vascular development and blood pressure elevation. No significant differences were observed in the expression of the RaA calp and SM22 mRNAs between normotensive (Wistar Kyoto) and spontaneously hypertensive rats (SHR).
引用
收藏
页码:297 / 302
页数:6
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