Beyond a platform protein for the degradosome assembly: The Apoptosis-Inducing Factor as an efficient nuclease involved in chromatinolysis

被引:20
|
作者
Novo, Nerea [1 ,2 ]
Romero-Tamayo, Silvia [1 ,2 ]
Marcuello, Carlos [3 ,4 ]
Boneta, Sergio [1 ]
Blasco-Machin, Irene [1 ]
Velazquez-Campoy, Adrian [1 ,2 ,5 ,6 ]
Villanueva, Raquel [1 ,2 ]
Moreno-Loshuertos, Raquel [1 ,2 ]
Lostao, Anabel [3 ,4 ,7 ]
Medina, Milagros [1 ,2 ]
Ferreira, Patricia [1 ,2 ]
机构
[1] Univ Zaragoza, Fac Ciencias, Dept Bioquim Biol Mol Celular, Zaragoza 50009, Spain
[2] Univ Zaragoza, BIFI GBsC CSIC Joint Unit, Inst Biocomputac & Fis Sist Complejos, Zaragoza 50018, Spain
[3] Univ Zaragoza, Inst Nanociencia Mat Aragon INMA, CSIC, Zaragoza 50009, Spain
[4] Univ Zaragoza, Lab Microscopias Avanzadas LMA, Zaragoza 50018, Spain
[5] Aragon Inst Hlth Res IIS Aragon, Zaragoza 50009, Spain
[6] Biomed Res Networking Ctr Liver & Digest Dis CIBR, Madrid 28029, Spain
[7] Fdn ARAID, Zaragoza 50018, Spain
来源
PNAS NEXUS | 2023年 / 2卷 / 02期
关键词
human Apoptosis-Inducing Factor; DNA-degradosome complex; nuclease activity; chromatinolysis; AIF; DNA; BINDING; PURIFICATION; PATHWAYS; MODE; H2AX;
D O I
10.1093/pnasnexus/pgac312
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Apoptosis-Inducing Factor (AIF) is amoonlighting 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 Mg2+ or Ca2+. 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.
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页数:11
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