Naitza Silvia, Rossé Carine, Kappler Christine, Georgel Philippe, Belvin Marcia, Gubb David, Camonis Jacques, Hoffmann Jules A, Reichhart Jean Marc
Institut de Biologie Moleculaire et Cellulaire, UPR 9022 du CNRS, 15 Rue René Descartes, 67084 Cedex, Strasbourg, France.
Immunity. 2002 Nov;17(5):575-81. doi: 10.1016/s1074-7613(02)00454-5.
Drosophila responds to Gram-negative infections by mounting an immune response that depends on components of the IMD pathway. We recently showed that imd encodes a protein with a death domain with high similarity to that of mammalian RIP. Using a two-hybrid screen in yeast, we have isolated the death protein dFADD as a molecule that associates with IMD. Our data show that loss of dFADD function renders flies highly susceptible to Gram-negative infections without affecting resistance to Gram-positive bacteria. By genetic analysis we show that dFADD acts downstream of IMD in the pathway that controls inducibility of the antibacterial peptide genes.
果蝇通过启动一种依赖于IMD途径成分的免疫反应来应对革兰氏阴性菌感染。我们最近发现,imd编码一种具有死亡结构域的蛋白质,该结构域与哺乳动物RIP的死亡结构域高度相似。利用酵母双杂交筛选,我们分离出死亡蛋白dFADD作为一种与IMD相互作用的分子。我们的数据表明,dFADD功能的丧失使果蝇对革兰氏阴性菌感染高度敏感,而不影响对革兰氏阳性菌的抗性。通过遗传分析,我们表明dFADD在控制抗菌肽基因诱导性的途径中位于IMD的下游发挥作用。