Moriguchi T, Kuroyanagi N, Yamaguchi K, Gotoh Y, Irie K, Kano T, Shirakabe K, Muro Y, Shibuya H, Matsumoto K, Nishida E, Hagiwara M
Department of Genetics and Molecular Biology, Institute for Virus Research, Kyoto University, Sakyo-ku, Kyoto 606-01, Japan.
J Biol Chem. 1996 Jun 7;271(23):13675-9. doi: 10.1074/jbc.271.23.13675.
A cDNA encoding a novel member of the mitogen-activated protein kinase kinase (MAPKK) family, MAPKK6, was isolated and found to encode a protein of 334 amino acids, with a calculated molecular mass of 37 kDa that is 79% identical to MKK3. MAPKK6 was shown to phosphorylate and specifically activate the p38/MPK2 subgroup of the mitogen-activated protein kinase superfamily and could be demonstrated to be phosphorylated and activated in vitro by TAK1, a recently identified MAPKK kinase. MKK3 was also shown to be a good substrate for TAK1 in vitro. Furthermore, when co-expressed with TAK1 in cells in culture, both MAPKK6 and MKK3 were strongly activated. In addition, co-expression of TAK1 and p38/MPK2 in cells resulted in activation of p38/MPK2. These results indicate the existence of a novel kinase cascade consisting of TAK1, MAPKK6/MKK3, and p38/MPK2.
编码有丝分裂原活化蛋白激酶激酶(MAPKK)家族新成员MAPKK6的互补DNA(cDNA)被分离出来,发现它编码一个含334个氨基酸的蛋白质,计算分子量为37 kDa,与MKK3有79%的同源性。研究表明,MAPKK6能磷酸化并特异性激活有丝分裂原活化蛋白激酶超家族的p38/MPK2亚组,并且在体外可被最近鉴定出的一种MAPKK激酶TAK1磷酸化并激活。体外实验还表明,MKK3也是TAK1的良好底物。此外,当在培养细胞中与TAK1共表达时,MAPKK6和MKK3均被强烈激活。另外,在细胞中共表达TAK1和p38/MPK2会导致p38/MPK2的激活。这些结果表明存在一个由TAK1、MAPKK6/MKK3和p38/MPK2组成的新型激酶级联反应。