Azevedo Dulce, Nascimento Liliana, Labarre Jean, Toledano Michel B, Rodrigues-Pousada Claudina
Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Apartado 127, 2780-901 Oeiras, Portugal.
FEBS Lett. 2007 Jan 23;581(2):187-95. doi: 10.1016/j.febslet.2006.11.083. Epub 2006 Dec 13.
Towards elucidating the function of Yap2, which remains unclear, we have taken advantage of the C-terminal homology between Yap1 and Yap2. Swapping domains experiments show that the Yap2 C-terminal domain functionally substitutes for the homologous Yap1 domain in the response to Cd, but not to H2O2. We conclude that specificity determinants of the Cd response are encoded within both Yap1 and Yap2 C-terminus, whereas those required for H2O2 response are only present in the Yap1 C-terminus. Furthermore, our results identify FRM2 as Cd-responsive Yap2 target and indicate a possible role of this protein in regulating a metal stress response.
为了阐明功能仍不清楚的Yap2的作用,我们利用了Yap1和Yap2之间的C端同源性。结构域交换实验表明,Yap2的C端结构域在对镉的反应中可功能性替代同源的Yap1结构域,但对过氧化氢则不能。我们得出结论,镉反应的特异性决定因素在Yap1和Yap2的C端均有编码,而过氧化氢反应所需的特异性决定因素仅存在于Yap1的C端。此外,我们的结果确定FRM2为镉反应性Yap2靶点,并表明该蛋白在调节金属应激反应中可能发挥作用。