Liu Wei-Kuang, Yen Pei-Fen, Chien Chia-Yi, Fann Ming-Ji, Su Jin-Yuan, Chou Chen-Kung
Institute of Microbiology and Immunology, National Yang-Ming University, 155, Sec. 2, Li-Rong Street, Pei-Tou, Taipei 11211, Taiwan, Republic of China.
Biochem J. 2004 Mar 15;378(Pt 3):867-76. doi: 10.1042/BJ20031736.
NF-kappaB (nuclear factor kappaB) proteins are key transcription factors that regulate gene expression in response to various extracellular stimuli. The pathway leading to the activation of NF-kappaB involves a complicated network that includes a number of signalling molecules. The recent identification of a wide range of negative regulators of NF-kappaB has given another layer of complexity in NF-kappaB activation. We and others have previously identified the protein ABIN-2 (A20 binding inhibitor of NF-kappaB 2) as an inhibitor of NF-kappaB activation. In the present paper, we demonstrate that ABIN-2 exerts its inhibitory function by blocking the interaction of RIP (receptor-interacting protein) with the downstream effector IKKgamma, a non-kinase component of the IkappaB (inhibitory kappaB) kinase complex. When overexpressed in cells, ABIN-2 bound to IKKgamma and prevented the association of IKKgamma with RIP. By a deletion mapping, a stretch of 50 amino acids on ABIN-2 is found to be essential for its interaction with IKKgamma. The ABIN-2 mutant that lacked these 50 amino acids did not interact with IKKgamma and, consequently, failed to inhibit NF-kappaB activation. Strikingly, a portion of RIP, which is similar to this 50-residue domain of ABIN-2, is also essential for RIP interaction with IKKgamma. The RIP mutant with deletion of this similar region did not associate with IKKgamma and had substantial reduction of its ability to mediate NF-kappaB activation. Taken together, these conserved 50 residues of ABIN-2 and RIP define a novel structural domain in mediating a key step in the NF-kappaB signalling pathway through the interaction with IKKgamma. Finally, the signalling pathway of NF-kappaB activation is known to promote survival in many cellular events. The mechanism for decision between cell death and survival is under fine regulation. In the present paper, we demonstrated further that the expression of ABIN-2 could promote the RIP-mediated apoptosis by presumably suppressing the anti-apoptotic effect of NF-kappaB.
核因子κB(NF-κB)蛋白是关键的转录因子,可响应各种细胞外刺激调节基因表达。导致NF-κB激活的信号通路涉及一个复杂的网络,其中包括许多信号分子。最近对多种NF-κB负调控因子的鉴定,使NF-κB激活过程更加复杂。我们和其他人之前已鉴定出蛋白ABIN-2(NF-κB 2的A20结合抑制剂)是NF-κB激活的抑制剂。在本文中,我们证明ABIN-2通过阻断RIP(受体相互作用蛋白)与下游效应分子IKKγ(IκB激酶复合物的非激酶成分)的相互作用发挥其抑制功能。当在细胞中过表达时,ABIN-2与IKKγ结合并阻止IKKγ与RIP结合。通过缺失定位,发现ABIN-2上一段50个氨基酸的片段对于其与IKKγ的相互作用至关重要。缺少这50个氨基酸的ABIN-2突变体不与IKKγ相互作用,因此无法抑制NF-κB激活。令人惊讶的是,RIP的一部分与ABIN-2的这个50个残基结构域相似,对于RIP与IKKγ的相互作用也至关重要。缺失该相似区域的RIP突变体不与IKKγ结合,并且其介导NF-κB激活的能力大幅降低。综上所述,ABIN-2和RIP中这些保守的50个残基通过与IKKγ相互作用,在介导NF-κB信号通路的关键步骤中定义了一个新的结构域。最后,已知NF-κB激活的信号通路在许多细胞事件中促进细胞存活。细胞死亡和存活之间的决定机制受到精细调控。在本文中,我们进一步证明ABIN-2的表达可能通过抑制NF-κB的抗凋亡作用来促进RIP介导的细胞凋亡。