Spencer D M, Graef I, Austin D J, Schreiber S L, Crabtree G R
Howard Hughes Medical Institute, Department of Developmental Biology, Stanford University Medical School, CA 94062, USA.
Proc Natl Acad Sci U S A. 1995 Oct 10;92(21):9805-9. doi: 10.1073/pnas.92.21.9805.
The Src-like tyrosine kinases require membrane localization for transformation and probably for their normal role in signal transduction. We utilized this characteristic to prepare Src-like tyrosine kinases that can be readily activated with the rationally designed chemical inducer of dimerization FK1012. Dimerization of cytoplasmic Src-like tyrosine kinases was not sufficient for signaling, but their recruitment to the plasma membrane led to the rapid activation of transcription factors identical to those regulated by crosslinking the antigen receptor. Moreover, recruitment of activated Src-like kinases to the membrane replaced signaling by the T-lymphocyte antigen receptor complex, leading to the activation of both the Ras/protein kinase C and Ca2+/calcineurin pathways normally activated by antigen receptor signaling. Since these chemical inducers of dimerization are cell permeable, this approach permits the production of conditional alleles of any of the Src-like tyrosine kinases, thereby allowing a delineation of their developmental roles.
类Src酪氨酸激酶需要定位于细胞膜才能发挥转化作用,可能在信号转导中也发挥正常作用。我们利用这一特性制备了类Src酪氨酸激酶,它们可以被合理设计的二聚化化学诱导剂FK1012轻易激活。细胞质类Src酪氨酸激酶的二聚化不足以引发信号传导,但将它们募集到质膜会导致转录因子的快速激活,这些转录因子与通过交联抗原受体所调控的转录因子相同。此外,将活化的类Src激酶募集到膜上取代了T淋巴细胞抗原受体复合物的信号传导,导致通常由抗原受体信号传导激活的Ras/蛋白激酶C和Ca2+/钙调神经磷酸酶途径均被激活。由于这些二聚化化学诱导剂可穿透细胞,这种方法允许产生任何类Src酪氨酸激酶的条件等位基因,从而能够描绘它们在发育中的作用。