These authors contributed equally.
New mechanistic insights into pre-protein transport across the second outermost plastid membrane of diatoms
Article first published online: 25 MAR 2010
© 2010 Blackwell Publishing Ltd
Volume 76, Issue 3, pages 793–801, May 2010
How to Cite
Hempel, F., Felsner, G. and Maier, U. G. (2010), New mechanistic insights into pre-protein transport across the second outermost plastid membrane of diatoms. Molecular Microbiology, 76: 793–801. doi: 10.1111/j.1365-2958.2010.07142.x
- Issue published online: 23 APR 2010
- Article first published online: 25 MAR 2010
- Accepted 15 March, 2010.
Chromalveolates like the diatom Phaeodactylum tricornutum arose through the uptake of a red alga by a phagotrophic protist, a process termed secondary endosymbiosis. In consequence, the plastids are surrounded by two additional membranes compared with primary plastids. This plastid morphology poses additional barriers for plastid-destined proteins, which are mostly nucleus-encoded. Recent investigations have focused on the postulated translocon of the second outermost membrane (periplastidal membrane, PPM). These studies identified a symbiont-specific ERAD (endoplasmic reticulum-associated degradation)-like machinery (SELMA), which has been implicated in plastid pre-protein import. Despite this recent progress, key factors for protein transport via SELMA are still unknown. As SELMA substrates presumably undergo ubiquitination, a corresponding ubiquitin ligase and an enzyme for the subsequent removal of ubiquitin need to reside in the space between the second and third membrane (periplastidal compartment, PPC). Here we characterize two proteins fulfilling these criteria. We show that ptE3P (P.t ricornutumE3 enzyme of the PPC), the ubiquitin ligase, and ptDUP (P.t ricornutumde-ubiquitinating enzyme of the PPC), the de-ubiquitinase, localize to the PPM and PPC, respectively. In addition, we demonstrate their retained functionality by in vitro data.