Caenorhabditis elegans Mitofilin Homologs Control the Morphology of Mitochondrial Cristae and Influence Reproduction and Physiology
DC Field | Value | Language |
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dc.contributor.author | Mun, Ji Young | - |
dc.contributor.author | Lee, Tae Hoon | - |
dc.contributor.author | Kim, Ji Hui | - |
dc.contributor.author | Yoo, Bum Ho | - |
dc.contributor.author | Bahk, Young Yil | - |
dc.contributor.author | Koo, Hyeon-Sook | - |
dc.contributor.author | Han, Sung Sik | - |
dc.date.accessioned | 2021-09-08T00:36:44Z | - |
dc.date.available | 2021-09-08T00:36:44Z | - |
dc.date.created | 2021-06-14 | - |
dc.date.issued | 2010-09 | - |
dc.identifier.issn | 0021-9541 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/115800 | - |
dc.description.abstract | Human mitofilin is a mitochondrial protein that controls cristae formation. Here, we investigated the role of the Caenorhabditis elegans mitofilin homologs, IMMT-1 and -2, in reproduction, physiology, and mitochondrial cristae formation. Mutation of either immt-1 or immt-2 produced defects in germline development and egg-laying. These defects were exacerbated by the double mutation, which greatly reduced motility, increased levels of reactive oxygen species, decreased mitochondrial mass, and imparted resistance to oxidative stress. Cryo-electron microscopy and electron tomography revealed that each of the single mutations resulted in curved and stacked mitochondrial crista tubules as well as a reduced number of crista junctions. The immt-2 mutation was also associated with the presence of outer mitochondrial membrane pores, which were larger in the double mutant. IMMT-1 and IMMT-2 proteins were localized to the inner mitochondrial membrane, as seen by immunoelectron microscopy, and they behaved as oligomers or large complexes with F1F0 ATP synthase in native polyacrylamide gel electrophoresis. These findings suggest that the two C. elegans mitofilin isoforms have non-overlapping functions in controlling mitochondrial cristae formation. J. Cell. Physiol.224: 748-756,2010. (C) 2010 Wiley-Liss, Inc. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | WILEY | - |
dc.subject | INNER MEMBRANE-PROTEIN | - |
dc.subject | YEAST ATP SYNTHASE | - |
dc.subject | COILED-COIL | - |
dc.subject | DYNAMICS | - |
dc.subject | FLUORESCENCE | - |
dc.subject | TOMOGRAPHY | - |
dc.subject | EXPRESSION | - |
dc.subject | APOPTOSIS | - |
dc.subject | GENE | - |
dc.title | Caenorhabditis elegans Mitofilin Homologs Control the Morphology of Mitochondrial Cristae and Influence Reproduction and Physiology | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Han, Sung Sik | - |
dc.identifier.doi | 10.1002/jcp.22177 | - |
dc.identifier.scopusid | 2-s2.0-77954573806 | - |
dc.identifier.wosid | 000280621600024 | - |
dc.identifier.bibliographicCitation | JOURNAL OF CELLULAR PHYSIOLOGY, v.224, no.3, pp.748 - 756 | - |
dc.relation.isPartOf | JOURNAL OF CELLULAR PHYSIOLOGY | - |
dc.citation.title | JOURNAL OF CELLULAR PHYSIOLOGY | - |
dc.citation.volume | 224 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | 748 | - |
dc.citation.endPage | 756 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Cell Biology | - |
dc.relation.journalResearchArea | Physiology | - |
dc.relation.journalWebOfScienceCategory | Cell Biology | - |
dc.relation.journalWebOfScienceCategory | Physiology | - |
dc.subject.keywordPlus | INNER MEMBRANE-PROTEIN | - |
dc.subject.keywordPlus | YEAST ATP SYNTHASE | - |
dc.subject.keywordPlus | COILED-COIL | - |
dc.subject.keywordPlus | DYNAMICS | - |
dc.subject.keywordPlus | FLUORESCENCE | - |
dc.subject.keywordPlus | TOMOGRAPHY | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | APOPTOSIS | - |
dc.subject.keywordPlus | GENE | - |
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