Mui A L, Wakao H, Harada N, O'Farrell A M, Miyajima A
Department of Cell Biology, DNAX Research Institute of Molecular and Cellular Biology, Palo Alto, California.
J Leukoc Biol. 1995 May;57(5):799-803. doi: 10.1002/jlb.57.5.799.
Recently, JAK2 kinase was found to be one of the tyrosine kinases activated by interleukin-3 (IL-3) in target cells. JAK2 belongs to a family of kinases that act upstream of transcription factors called STATs. STATs exist in the cytoplasm as latent, transcriptionally inactive forms until, in response to extracellular signals, they become phosphorylated on tyrosine residues, translocate to the nucleus, and bind to specific DNA elements. Because IL-3 activates JAK2, we searched for the STAT(s) that might transduce IL-3 signals. Several lines of evidence suggest that IL-3 uses the murine homologue of STAT5, a factor originally purified from sheep. Unexpectedly, during isolation of the murine homologue, we found two highly related molecules that we have designated STAT5A and STAT5B.
最近,人们发现JAK2激酶是白细胞介素-3(IL-3)在靶细胞中激活的酪氨酸激酶之一。JAK2属于一类激酶家族,其作用于被称为信号转导和转录激活因子(STATs)的转录因子上游。STATs以潜伏的、转录无活性的形式存在于细胞质中,直到响应细胞外信号时,它们在酪氨酸残基上被磷酸化,转位至细胞核,并与特定的DNA元件结合。由于IL-3激活JAK2,我们寻找了可能转导IL-3信号的STAT。几条证据表明IL-3使用STAT5的小鼠同源物,STAT5是最初从绵羊中纯化出来的一种因子。出乎意料的是,在分离小鼠同源物的过程中,我们发现了两个高度相关的分子,我们将其命名为STAT5A和STAT5B。