scholarly journals Parkin-mediated ubiquitination contributes to the constitutive turnover of mitochondrial fission factor (Mff)

2019 ◽  
Author(s):  
Laura Lee ◽  
Richard Seager ◽  
Kevin A. Wilkinson ◽  
Jeremy M. Henley

AbstractThe mitochondrial outer membrane protein Mitochondrial Fission Factor (Mff) plays a key role in both physiological and pathological fission. It is well established that in stressed or functionally impaired mitochondria the PINK1 recruits the ubiquitin ligase Parkin which ubiquitinates Mff to facilitate the removal of defective mitochondria and maintain the integrity mitochondrial network. Here we show that, in addition to this clearance pathway, Parkin also ubiquitinates Mff in a PINK1-dependent manner under basal, non-stressed conditions to regulate constitutive Mff turnover. We further show that removing Parkin with shRNA knockdown does not completely prevent Mff ubiquitination under these conditions indicating that at least one other ubiquitin ligase contributes to Mff proteostasis. These data demonstrate that Parkin plays a role in physiological maintenance of mitochondrial membrane protein composition in healthy mitochondria through constitutive low-level activation.

2014 ◽  
Vol 25 (1) ◽  
pp. 145-159 ◽  
Author(s):  
Qinfang Shen ◽  
Koji Yamano ◽  
Brian P. Head ◽  
Sumihiro Kawajiri ◽  
Jesmine T. M. Cheung ◽  
...  

Mitochondrial fission is mediated by the dynamin-related protein Drp1 in metazoans. Drp1 is recruited from the cytosol to mitochondria by the mitochondrial outer membrane protein Mff. A second mitochondrial outer membrane protein, named Fis1, was previously proposed as recruitment factor, but Fis1−/− cells have mild or no mitochondrial fission defects. Here we show that Fis1 is nevertheless part of the mitochondrial fission complex in metazoan cells. During the fission cycle, Drp1 first binds to Mff on the surface of mitochondria, followed by entry into a complex that includes Fis1 and endoplasmic reticulum (ER) proteins at the ER–mitochondrial interface. Mutations in Fis1 do not normally affect fission, but they can disrupt downstream degradation events when specific mitochondrial toxins are used to induce fission. The disruptions caused by mutations in Fis1 lead to an accumulation of large LC3 aggregates. We conclude that Fis1 can act in sequence with Mff at the ER–mitochondrial interface to couple stress-induced mitochondrial fission with downstream degradation processes.


2019 ◽  
Vol 7 (1) ◽  
pp. 120-121 ◽  
Author(s):  
Afagh Alavi ◽  
Mahisa Mokhtari ◽  
Reza Hajati ◽  
Atefeh Davarzani ◽  
Alfonso Fasano ◽  
...  

Aging Cell ◽  
2014 ◽  
Vol 13 (3) ◽  
pp. 507-518 ◽  
Author(s):  
Ran Lin ◽  
Alessia Angelin ◽  
Federico Da Settimo ◽  
Claudia Martini ◽  
Sabrina Taliani ◽  
...  

2017 ◽  
Vol 28 (3) ◽  
pp. 385-392 ◽  
Author(s):  
Marta Skowronska ◽  
Tomasz Kmiec ◽  
Anna Czlonkowska ◽  
Iwona Kurkowska-Jastrzębska

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