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Regulation of peroxisome dynamics by phosphorylation.

Authors :
Oeljeklaus, Silke
Schummer, Andreas
Mastalski, Thomas
Platta, Harald W.
Warscheid, Bettina
Source :
BBA - Molecular Cell Research. May2016, Vol. 1863 Issue 5, p1027-1037. 11p.
Publication Year :
2016

Abstract

Peroxisomes are highly dynamic organelles that can rapidly change in size, abundance, and protein content in response to alterations in nutritional and other environmental conditions. These dynamic changes in peroxisome features, referred to as peroxisome dynamics, rely on the coordinated action of several processes of peroxisome biogenesis. Revealing the regulatory mechanisms of peroxisome dynamics is an emerging theme in cell biology. These mechanisms are inevitably linked to and synchronized with the biogenesis and degradation of peroxisomes. To date, the key players and basic principles of virtually all steps in the peroxisomal life cycle are known, but regulatory mechanisms remained largely elusive. A number of recent studies put the spotlight on reversible protein phosphorylation for the control of peroxisome dynamics and highlighted peroxisomes as hubs for cellular signal integration and regulation. Here, we will present and discuss the results of several studies performed using yeast and mammalian cells that convey a sense of the impact protein phosphorylation may have on the modulation of peroxisome dynamics by regulating peroxisomal matrix and membrane protein import, proliferation, inheritance, and degradation. We further put forward the idea to make use of current data on phosphorylation sites of peroxisomal and peroxisome-associated proteins reported in advanced large-scale phosphoproteomic studies. This article is part of a Special Issue entitled: Peroxisomes edited by Ralf Erdmann. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01674889
Volume :
1863
Issue :
5
Database :
Academic Search Index
Journal :
BBA - Molecular Cell Research
Publication Type :
Academic Journal
Accession number :
113896476
Full Text :
https://doi.org/10.1016/j.bbamcr.2015.12.022