Mff functions with Pex11pβ and DLP1 in peroxisomal fission

Akinori Itoyama, Satoru Michiyuki, Masanori Honsho, Taizo Yamamoto, Ann Moser, Yumi Yoshida, Yukio Fujiki

Research output: Contribution to journalArticlepeer-review

40 Scopus citations


Peroxisomal division comprises three steps: elongation, constriction, and fission. Translocation of dynamin-like protein 1 (DLP1), a member of the large GTPase family, from the cytosol to peroxisomes is a prerequisite for membrane fission; however, the molecular machinery for peroxisomal targeting of DLP1 remains unclear. This study investigated whether mitochondrial fission factor (Mff), which targets DLP1 to mitochondria, may also recruit DLP1 to peroxisomes. Results show that endogenous Mff is localized to peroxisomes, especially at the membrane-constricted regions of elongated peroxisomes, in addition to mitochondria. Knockdown of MFF abrogates the fission stage of peroxisomal division and is associated with failure to recruit DLP1 to peroxisomes, while ectopic expression of MFF increases the peroxisomal targeting of DLP1. Co-expression of MFF and PEX11β, the latter being a key player in peroxisomal elongation, increases peroxisome abundance. Overexpression of MFF also increases the interaction between DLP1 and Pex11pβ, which knockdown of MFF, but not Fis1, abolishes. Moreover, results show that Pex11pβ interacts with Mff in a DLP1-dependent manner. In conclusion, Mff contributes to the peroxisomal targeting of DLP1 and plays a key role in the fission of the peroxisomal membrane by acting in concert with Pex11pβ and DLP1.

Original languageEnglish (US)
Pages (from-to)998-1006
Number of pages9
JournalBiology Open
Issue number10
StatePublished - Oct 15 2013


  • Division
  • Dynamin-like protein 1
  • Elongation
  • Fis1
  • Fission
  • Mitochondrial fission factor
  • Peroxin Pex11p
  • Peroxisome morphogenesis

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology
  • General Agricultural and Biological Sciences


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