Yamaguchi K, Shirakabe K, Shibuya H, Irie K, Oishi I, Ueno N, Taniguchi T, Nishida E, Matsumoto K
Department of Molecular Biology, Faculty of Science, Nagoya University, Japan.
Science. 1995 Dec 22;270(5244):2008-11. doi: 10.1126/science.270.5244.2008.
The mitogen-activated protein kinase (MAPK) pathway is a conserved eukaryotic signaling module that converts receptor signals into various outputs. MAPK is activated through phosphorylation by MAPK kinase (MAPKK), which is first activated by MAPKK kinase (MAPKKK). A genetic selection based on a MAPK pathway in yeast was used to identify a mouse protein kinase (TAK1) distinct from other members of the MAPKKK family. TAK1 was shown to participate in regulation of transcription by transforming growth factor-beta (TGF-beta). Furthermore, kinase activity of TAK1 was stimulated in response to TGF-beta and bone morphogenetic protein. These results suggest that TAK1 functions as a mediator in the signaling pathway of TGF-beta superfamily members.
丝裂原活化蛋白激酶(MAPK)通路是一种保守的真核信号传导模块,可将受体信号转化为各种输出。MAPK通过MAPK激酶(MAPKK)磷酸化而被激活,而MAPKK首先由MAPKK激酶(MAPKKK)激活。基于酵母中MAPK通路的遗传筛选被用于鉴定一种不同于MAPKKK家族其他成员的小鼠蛋白激酶(TAK1)。TAK1被证明参与转化生长因子-β(TGF-β)对转录的调控。此外,TAK1的激酶活性在对TGF-β和骨形态发生蛋白的反应中受到刺激。这些结果表明TAK1在TGF-β超家族成员的信号通路中起介质作用。