IGBMC (Institut de Génétique et de Biologie Moléculaire et Cellulaire) Translational Medicine and Neurogenetics Department, 67404 Illkirch, France.
Inserm U596, 67404 Illkirch, France.
Nat Commun. 2017 May 11;8:15124. doi: 10.1038/ncomms15124.
Mammalian A-type proteins, ISCA1 and ISCA2, are evolutionarily conserved proteins involved in iron-sulfur cluster (Fe-S) biogenesis. Recently, it was shown that ISCA1 and ISCA2 form a heterocomplex that is implicated in the maturation of mitochondrial FeS proteins. Here we report that mouse ISCA1 and ISCA2 are FeS-containing proteins that combine all features of Fe-S carrier proteins. We use biochemical, spectroscopic and in vivo approaches to demonstrate that despite forming a complex, ISCA1 and ISCA2 establish discrete interactions with components of the late Fe-S machinery. Surprisingly, knockdown experiments in mouse skeletal muscle and in primary cultures of neurons suggest that ISCA1, but not ISCA2, is required for mitochondrial FeS proteins biogenesis. Collectively, our data suggest that cellular processes with different requirements for ISCA1, ISCA2 and ISCA1-ISCA2 complex seem to exist.
哺乳动物 A 型蛋白 ISCA1 和 ISCA2 是参与铁硫簇(Fe-S)生物发生的进化保守蛋白。最近的研究表明,ISCA1 和 ISCA2 形成了一种异源复合物,该复合物与线粒体 Fe-S 蛋白的成熟有关。本文报道了小鼠 ISCA1 和 ISCA2 是含有 Fe-S 的蛋白,它们具有 Fe-S 载体蛋白的所有特征。我们使用生化、光谱和体内方法证明,尽管形成复合物,但 ISCA1 和 ISCA2 与晚期 Fe-S 机器的组件建立了离散的相互作用。令人惊讶的是,在小鼠骨骼肌和神经元原代培养物中的敲低实验表明,ISCA1,但不是 ISCA2,是线粒体 Fe-S 蛋白生物发生所必需的。总之,我们的数据表明,细胞的不同过程可能需要 ISCA1、ISCA2 和 ISCA1-ISCA2 复合物来完成。