Clavier Amandine, Rincheval-Arnold Aurore, Baillet Adrienne, Mignotte Bernard, Guénal Isabelle
a Université de Versailles Saint-Quentin-en-Yvelines, Laboratoire de Génétique et Biologie Cellulaire , EA4589 , Montigny-le-Bretonneux ; France.
b Ecole Pratique des Hautes Etudes, Laboratoire de Génétique Moléculaire et Physiologique , Montigny-le-Bretonneux , France.
Cell Cycle. 2016;15(2):283-94. doi: 10.1080/15384101.2015.1100776.
The Jun Kinase (JNK) signaling pathway responds to diverse stimuli by appropriate and specific cellular responses such as apoptosis, differentiation or proliferation. The mechanisms that mediate this specificity remain largely unknown. The core of this signaling pathway, composed of a JNK protein and a JNK kinase (JNKK), can be activated by various putative JNKK kinases (JNKKK) which are themselves downstream of different adaptor proteins. A proposed hypothesis is that the JNK pathway specific response lies in the combination of a JNKKK and an adaptor protein upstream of the JNKK. We previously showed that the Drosophila homolog of pRb (Rbf1) and a mutant form of Rbf1 (Rbf1(D253A)) have JNK-dependent pro-apoptotic properties. Rbf1(D253A) is also able to induce a JNK-dependent abnormal proliferation. Here, we show that Rbf1-induced apoptosis triggers proliferation which depends on the JNK pathway activation. Taking advantage of these phenotypes, we investigated the JNK signaling involved in either Rbf1-induced apoptosis or in proliferation in response to Rbf1-induced apoptosis. We demonstrated that 2 different JNK pathways involving different adaptor proteins and kinases are involved in Rbf1-apoptosis (i.e. Rac1-dTak1-dMekk1-JNK pathway) and in proliferation in response to Rbf1-induced apoptosis (i.e., dTRAF1-Slipper-JNK pathway). Using a transient induction of rbf1, we show that Rbf1-induced apoptosis activates a compensatory proliferation mechanism which also depends on Slipper and dTRAF1. Thus, these 2 proteins seem to be key players of compensatory proliferation in Drosophila.
JNK信号通路通过诸如凋亡、分化或增殖等适当且特定的细胞反应来应对多种刺激。介导这种特异性的机制在很大程度上仍不清楚。该信号通路的核心由JNK蛋白和JNK激酶(JNKK)组成,可被各种假定的JNKK激酶(JNKKK)激活,而这些激酶本身位于不同衔接蛋白的下游。一个提出的假说是,JNK通路的特异性反应在于JNKK上游的JNKKK和衔接蛋白的组合。我们之前表明,果蝇中pRb的同源物(Rbf1)和Rbf1的一种突变形式(Rbf1(D253A))具有JNK依赖性的促凋亡特性。Rbf1(D253A)也能够诱导JNK依赖性的异常增殖。在这里,我们表明Rbf1诱导的凋亡触发了依赖于JNK通路激活的增殖。利用这些表型,我们研究了参与Rbf1诱导的凋亡或对Rbf1诱导凋亡的增殖反应中的JNK信号传导。我们证明,涉及不同衔接蛋白和激酶的2种不同JNK通路参与了Rbf1诱导的凋亡(即Rac1-dTak1-dMekk1-JNK通路)以及对Rbf1诱导凋亡的增殖反应(即dTRAF1-Slipper-JNK通路)。通过短暂诱导rbf1,我们表明Rbf1诱导的凋亡激活了一种也依赖于Slipper和dTRAF1的代偿性增殖机制。因此,这2种蛋白似乎是果蝇代偿性增殖的关键参与者。