Garcia Christian Joel, Khajeh Jahan, Coulanges Emmanuel, Chen Emily I-Ju, Owusu-Ansah Edward
Department of Physiology and Cellular Biophysics, Columbia University Medical Center, New York, NY 10032, USA.
Proteomics Shared Resource at the Herbert Irving Comprehensive Cancer Center and Department of Pharmacology, Columbia University Medical Center, New York, NY 10032, USA.
Cell Rep. 2017 Jul 5;20(1):264-278. doi: 10.1016/j.celrep.2017.06.015.
The flight muscles of Drosophila are highly enriched with mitochondria, but the mechanism by which mitochondrial complex I (CI) is assembled in this tissue has not been described. We report the mechanism of CI biogenesis in Drosophila flight muscles and show that it proceeds via the formation of ∼315, ∼550, and ∼815 kDa CI assembly intermediates. Additionally, we define specific roles for several CI subunits in the assembly process. In particular, we show that dNDUFS5 is required for converting an ∼700 kDa transient CI assembly intermediate into the ∼815 kDa assembly intermediate. Importantly, incorporation of dNDUFS5 into CI is necessary to stabilize or promote incorporation of dNDUFA10 into the complex. Our findings highlight the potential of studies of CI biogenesis in Drosophila to uncover the mechanism of CI assembly in vivo and establish Drosophila as a suitable model organism and resource for addressing questions relevant to CI biogenesis in humans.
果蝇的飞行肌肉富含线粒体,但线粒体复合物I(CI)在该组织中的组装机制尚未见报道。我们报告了果蝇飞行肌肉中CI生物发生的机制,并表明它通过形成约315、约550和约815 kDa的CI组装中间体进行。此外,我们定义了几个CI亚基在组装过程中的特定作用。特别是,我们表明dNDUFS5是将约700 kDa的瞬时CI组装中间体转化为约815 kDa组装中间体所必需的。重要的是,将dNDUFS5掺入CI对于稳定或促进dNDUFA10掺入复合物是必要的。我们的研究结果突出了果蝇中CI生物发生研究在揭示体内CI组装机制方面的潜力,并将果蝇确立为解决与人类CI生物发生相关问题的合适模式生物和资源。