Owaki H, Makar R, Boulton T G, Cobb M H, Geppert T D
Harold C. Simmons Arthritis Research Center, University of Texas Southwestern Medical Center, Dallas 75235-8884.
Biochem Biophys Res Commun. 1992 Feb 14;182(3):1416-22. doi: 10.1016/0006-291x(92)91891-s.
Extracellular signal-regulated kinases 1 and 2 are growth factor-sensitive serine/threonine kinases. cDNAs for both human kinases were isolated and sequenced. The nucleic acid and deduced protein sequences of human extracellular signal-regulated kinase 1 were 88% and 96% identical, respectively, to the homologous rat sequences. The nucleic acid and deduced protein sequences of human extracellular signal-regulated kinase 2 were 90% and 98% identical, respectively, to the corresponding rat sequences. A human extracellular signal-regulated kinase 2 specific probe was used to demonstrate that the mRNA for this kinase was present in T cells and did not change with activation. The deduced protein sequences of both human kinases were greater than 95% identical to two Xenopus kinase sequences, indicating that these enzymes are highly conserved across species.
细胞外信号调节激酶1和2是对生长因子敏感的丝氨酸/苏氨酸激酶。分离并测序了两种人类激酶的cDNA。人类细胞外信号调节激酶1的核酸序列和推导的蛋白质序列分别与同源大鼠序列有88%和96%的同一性。人类细胞外信号调节激酶2的核酸序列和推导的蛋白质序列分别与相应大鼠序列有90%和98%的同一性。使用一种人类细胞外信号调节激酶2特异性探针来证明该激酶的mRNA存在于T细胞中,并且不会随激活而改变。两种人类激酶推导的蛋白质序列与两个非洲爪蟾激酶序列的同一性大于95%,表明这些酶在物种间高度保守。