Hozak R R, Manji G A, Friesen P D
Department of Biochemistry and Institute for Molecular Virology, Graduate School and College of Agricultural and Life Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Mol Cell Biol. 2000 Mar;20(5):1877-85. doi: 10.1128/MCB.20.5.1877-1885.2000.
The defining structural motif of the inhibitor of apoptosis (iap) protein family is the BIR (baculovirus iap repeat), a highly conserved zinc coordination domain of approximately 70 residues. Although the BIR is required for inhibitor-of-apoptosis (IAP) function, including caspase inhibition, its molecular role in antiapoptotic activity in vivo is unknown. To define the function of the BIRs, we investigated the activity of these structural motifs within Op-IAP, an efficient, virus-derived IAP. We report here that Op-IAP(1-216), a loss-of-function truncation which contains two BIRs but lacks the C-terminal RING motif, potently interfered with Op-IAP's capacity to block apoptosis induced by diverse stimuli. In contrast, Op-IAP(1-216) had no effect on apoptotic suppression by caspase inhibitor P35. Consistent with a mechanism of dominant inhibition that involves direct interaction between Op-IAP(1-216) and full-length Op-IAP, both proteins formed an immunoprecipitable complex in vivo. Op-IAP also self-associated. In contrast, the RING motif-containing truncation Op-IAP(183-268) failed to interact with or interfere with Op-IAP function. Substitution of conserved residues within BIR 2 caused loss of dominant inhibition by Op-IAP(1-216) and coincided with loss of interaction with Op-IAP. Thus, residues encompassing the BIRs mediate dominant inhibition and oligomerization of Op-IAP. Consistent with dominant interference by interaction with an endogenous cellular IAP, Op-IAP(1-216) also lowered the survival threshold of cultured insect cells. Taken together, these data suggest a new model wherein the antiapoptotic function of IAP requires homo-oligomerization, which in turn mediates specific interactions with cellular apoptotic effectors.
凋亡抑制蛋白(IAP)家族的标志性结构基序是杆状病毒IAP重复序列(BIR),它是一个由约70个残基组成的高度保守的锌配位结构域。尽管BIR是凋亡抑制蛋白(IAP)功能所必需的,包括对半胱天冬酶的抑制作用,但其在体内抗凋亡活性中的分子作用尚不清楚。为了确定BIR的功能,我们研究了Op-IAP(一种高效的、病毒来源的IAP)中这些结构基序的活性。我们在此报告,Op-IAP(1-216)是一种功能缺失的截短体,它包含两个BIR,但缺乏C末端的RING基序,能有效干扰Op-IAP阻断多种刺激诱导的细胞凋亡的能力。相比之下,Op-IAP(1-216)对胱天蛋白酶抑制剂P35介导的凋亡抑制没有影响。与涉及Op-IAP(1-216)与全长Op-IAP直接相互作用的显性抑制机制一致,这两种蛋白在体内形成了可免疫沉淀的复合物。Op-IAP也能自我缔合。相比之下,含RING基序的截短体Op-IAP(183-268)未能与Op-IAP相互作用或干扰其功能。BIR 2内保守残基的替换导致Op-IAP(1-216)失去显性抑制作用,同时也失去了与Op-IAP的相互作用。因此,包含BIR的残基介导了Op-IAP的显性抑制和寡聚化。与通过与内源性细胞IAP相互作用产生的显性干扰一致,Op-IAP(1-216)也降低了培养昆虫细胞的存活阈值。综上所述,这些数据提示了一个新的模型,其中IAP的抗凋亡功能需要同源寡聚化,而这反过来又介导了与细胞凋亡效应器的特异性相互作用。