期刊
CURRENT BIOLOGY
卷 20, 期 14, 页码 1310-1315出版社
CELL PRESS
DOI: 10.1016/j.cub.2010.05.066
关键词
-
资金
- Heart and Stroke Foundation of Canada
- Canadian Institutes of Health
Mitochondria-derived vesicles (MDVs) have been shown to transport cargo from the mitochondria to the peroxisomes [1]. Mitochondria and peroxisomes share common functions in the oxidation of fatty acids and the reduction of damaging peroxides [2, 3]. Their biogenesis is also linked through both the activation of master transcription factors such as PGC-1 alpha [4, 5] and the common use of fission machinery, including DRP1, Mff, and hFis1 [6-9]. We have previously shown that MDVs are formed independently of the known mitochondria! fission GTPase Drp1 and are enriched for a mitochondrial small ubiquitin-like modifier (SUMO) E3 ligase called MAPL (mitochondrial-anchored protein ligase) [1]. Here, we demonstrate that the retromer complex, a known component of vesicle transport from the endosome to the Golgi apparatus [10-13], regulates the transport of MAPL from mitochondria to peroxisomes. An unbiased screen shows that Vps35 and Vps26 are found in complex with MAPL, and confocal imaging reveals Vps35 recruitment to mitochondria! vesicles. Silencing of Vps35 or Vps26A leads to a significant reduction in the delivery of MAPL to peroxisomes, placing the retromer within a novel intracellular trafficking route and providing insight into the formation of MAPL-positive MDVs.
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