Ghiglione C, Carraway K L, Amundadottir L T, Boswell R E, Perrimon N, Duffy J B
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Cell. 1999 Mar 19;96(6):847-56. doi: 10.1016/s0092-8674(00)80594-2.
We have identified the Drosophila transmembrane molecule kekkon 1 (kek1) as an inhibitor of the epidermal growth factor receptor (EGFR) and demonstrate that it acts in a negative feedback loop to modulate the activity of the EGFR tyrosine kinase. During oogenesis, kek1 is expressed in response to the Gurken/EGFR signaling pathway, and loss of kek1 activity is associated with an increase in EGFR signaling. Consistent with our loss-of-function studies, we demonstrate that ectopic overexpression of kek1 mimics a loss of EGFR activity. We show that the extracellular and transmembrane domains of Kek1 can inhibit and physically associate with the EGFR, suggesting potential models for this inhibitory mechanism.
我们已确定果蝇跨膜分子kekkon 1(kek1)是表皮生长因子受体(EGFR)的抑制剂,并证明它在负反馈回路中发挥作用,以调节EGFR酪氨酸激酶的活性。在卵子发生过程中,kek1响应Gurken/EGFR信号通路而表达,kek1活性丧失与EGFR信号增加有关。与我们的功能丧失研究一致,我们证明kek1的异位过表达模拟了EGFR活性的丧失。我们表明,Kek1的细胞外和跨膜结构域可以抑制EGFR并与其发生物理结合,这为这种抑制机制提供了潜在模型。