| Literature DB >> 28808085 |
Mira Sastri1, Manjula Darshi2, Mason Mackey3, Ranjan Ramachandra3, Saeyeon Ju3, Sebastien Phan3, Stephen Adams4, Kathryn Stein1, Christopher R Douglas1, Jiwan John Kim1, Mark H Ellisman3, Susan S Taylor1,2,4, Guy A Perkins5.
Abstract
Each mitochondrial compartment contains varying protein compositions that underlie a diversity of localized functions. Insights into the localization of mitochondrial intermembrane space-bridging (MIB) components will have an impact on our understanding of mitochondrial architecture, dynamics and function. By using the novel visualizable genetic tags miniSOG and APEX2 in cultured mouse cardiac and human astrocyte cell lines and performing electron tomography, we have mapped at nanoscale resolution three key MIB components, Mic19, Mic60 and Sam50 (also known as CHCHD3, IMMT and SAMM50, respectively), in the environment of structural landmarks such as cristae and crista junctions (CJs). Tagged Mic19 and Mic60 were located at CJs, distributed in a network pattern along the mitochondrial periphery and also enriched inside cristae. We discovered an association of Mic19 with cytochrome c oxidase subunit IV. It was also found that tagged Sam50 is not uniformly distributed in the outer mitochondrial membrane and appears to incompletely overlap with Mic19- or Mic60-positive domains, most notably at the CJs.Entities:
Keywords: APEX; Crista junction; Cristae; EFTEM; MICOS; miniSOG
Mesh:
Substances:
Year: 2017 PMID: 28808085 PMCID: PMC5665436 DOI: 10.1242/jcs.201400
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285