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Intra-plastid Protein Trafficking: How Plant Cells Adapted Prokaryotic Mechanisms to the Eukaryotic Condition

Overview
Specialties Biochemistry
Biophysics
Date 2012 Jul 4
PMID 22750312
Citations 56
Authors
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Abstract

Protein trafficking and localization in plastids involve a complex interplay between ancient (prokaryotic) and novel (eukaryotic) translocases and targeting machineries. During evolution, ancient systems acquired new functions and novel translocation machineries were developed to facilitate the correct localization of nuclear encoded proteins targeted to the chloroplast. Because of its post-translational nature, targeting and integration of membrane proteins posed the biggest challenge to the organelle to avoid aggregation in the aqueous compartments. Soluble proteins faced a different kind of problem since some had to be transported across three membranes to reach their destination. Early studies suggested that chloroplasts addressed these issues by adapting ancient-prokaryotic machineries and integrating them with novel-eukaryotic systems, a process called 'conservative sorting'. In the last decade, detailed biochemical, genetic, and structural studies have unraveled the mechanisms of protein targeting and localization in chloroplasts, suggesting a highly integrated scheme where ancient and novel systems collaborate at different stages of the process. In this review we focus on the differences and similarities between chloroplast ancestral translocases and their prokaryotic relatives to highlight known modifications that adapted them to the eukaryotic situation. This article is part of a Special Issue entitled: Protein Import and Quality Control in Mitochondria and Plastids.

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References
1.
Cline K, McCaffery M . Evidence for a dynamic and transient pathway through the TAT protein transport machinery. EMBO J. 2007; 26(13):3039-49. PMC: 1914107. DOI: 10.1038/sj.emboj.7601759. View

2.
Cline K . Import of proteins into chloroplasts. Membrane integration of a thylakoid precursor protein reconstituted in chloroplast lysates. J Biol Chem. 1986; 261(31):14804-10. View

3.
Hartl F, Schmidt B, Wachter E, Weiss H, Neupert W . Transport into mitochondria and intramitochondrial sorting of the Fe/S protein of ubiquinol-cytochrome c reductase. Cell. 1986; 47(6):939-51. DOI: 10.1016/0092-8674(86)90809-3. View

4.
Bruser T, Sanders C . An alternative model of the twin arginine translocation system. Microbiol Res. 2003; 158(1):7-17. DOI: 10.1078/0944-5013-00176. View

5.
Marty N, Rajalingam D, Kight A, Lewis N, Fologea D, Kumar T . The membrane-binding motif of the chloroplast signal recognition particle receptor (cpFtsY) regulates GTPase activity. J Biol Chem. 2009; 284(22):14891-903. PMC: 2685671. DOI: 10.1074/jbc.M900775200. View