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Protein Targeting into Secondary Plastids
被引:75
作者:
Bolte, Kathrin
[1
]
Bullmann, Lars
[1
]
Hempel, Franziska
[1
]
Bozarth, Andrew
[1
]
Zauner, Stefan
[1
]
Maier, Uwe-G.
[1
]
机构:
[1] Univ Marburg, Cell Biol Lab, D-35032 Marburg, Germany
关键词:
Protein transport;
secondarily evolved plastids;
secondary endosymbiosis;
LIGHT-HARVESTING PROTEINS;
NUCLEAR-ENCODED PROTEINS;
COMPLEX DIATOM PLASTIDS;
PLASMODIUM-FALCIPARUM;
TOXOPLASMA-GONDII;
CHLOROPLAST TRANSPORT;
SECRETORY PATHWAY;
IMPORT PATHWAYS;
GENE-TRANSFER;
GENOME;
D O I:
10.1111/j.1550-7408.2008.00370.x
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Most of the coding capacity of primary plastids is reserved for expressing some central components of the photosynthesis machinery and the translation apparatus. Thus, for the bulk of biochemical and cell biological reactions performed within the primary plastids, many nucleus-encoded components have to be transported posttranslationally into the organelle. The same is true for plastids surrounded by more than two membranes, where additional cellular compartments have to be supplied with nucleus-encoded proteins, leading to a corresponding increase in complexity of topogenic signals, transport and sorting machineries. In this review, we summarize recent progress in elucidating protein transport across up to five plastid membranes in plastids evolved in secondary endosymbiosis. Current data indicate that the mechanisms for protein transport across multiple membranes have evolved by altering pre-existing ones to new requirements in secondary plastids.
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页码:9 / 15
页数:7
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