Novo Nerea, Romero-Tamayo Silvia, Marcuello Carlos, Boneta Sergio, Blasco-Machin Irene, Velázquez-Campoy Adrián, Villanueva Raquel, Moreno-Loshuertos Raquel, Lostao Anabel, Medina Milagros, Ferreira Patricia
Departamento de Bioquímica y Biología Molecular y Celular, Facultad de Ciencias, Universidad de Zaragoza, Zaragoza 50009, Spain.
Instituto de Biocomputación y Física de Sistemas Complejos, BIFI (GBsC-CSIC Joint Unit), Universidad de Zaragoza, Zaragoza 50018, Spain.
PNAS Nexus. 2022 Dec 26;2(2):pgac312. doi: 10.1093/pnasnexus/pgac312. eCollection 2023 Feb.
The Apoptosis-Inducing Factor (AIF) is a moonlighting flavoenzyme involved in the assembly of mitochondrial respiratory complexes in healthy cells, but also able to trigger DNA cleavage and parthanatos. Upon apoptotic-stimuli, AIF redistributes from the mitochondria to the nucleus, where upon association with other proteins such as endonuclease CypA and histone H2AX, it is proposed to organize a DNA-degradosome complex. In this work, we provide evidence for the molecular assembly of this complex as well as for the cooperative effects among its protein components to degrade genomic DNA into large fragments. We have also uncovered that AIF has nuclease activity that is stimulated in the presence of either Mg or Ca. Such activity allows AIF by itself and in cooperation with CypA to efficiently degrade genomic DNA. Finally, we have identified TopIB and DEK motifs in AIF as responsible for its nuclease activity. These new findings point, for the first time, to AIF as a nuclease able to digest nuclear dsDNA in dying cells, improving our understanding of its role in promoting apoptosis and opening paths for the development of new therapeutic strategies.
凋亡诱导因子(AIF)是一种具有多种功能的黄素酶,在健康细胞中参与线粒体呼吸复合物的组装,但也能够引发DNA切割和PARP-1依赖性细胞坏死。在凋亡刺激下,AIF从线粒体重新分布到细胞核,在那里与其他蛋白质如核酸内切酶CypA和组蛋白H2AX结合后,有人提出它会组织形成一个DNA降解体复合物。在这项工作中,我们提供了该复合物分子组装的证据,以及其蛋白质成分之间协同作用将基因组DNA降解为大片段的证据。我们还发现AIF具有核酸酶活性,在Mg或Ca存在下会被激活。这种活性使AIF自身并与CypA协同作用,能够有效地降解基因组DNA。最后,我们确定了AIF中的TopIB和DEK基序是其核酸酶活性的原因。这些新发现首次指出AIF是一种能够在垂死细胞中消化核双链DNA的核酸酶,增进了我们对其在促进细胞凋亡中作用的理解,并为新治疗策略的开发开辟了道路。