Photosystem II assembly and repair are differentially localized in Chlamydomonas.

Plant Cell

Biology Department, Concordia University, Montreal, Quebec, Canada H4B 1R6.

Published: November 2007

Many proteins of the photosynthesis complexes are encoded by the genome of the chloroplast and synthesized by bacterium-like ribosomes within this organelle. To determine where proteins are synthesized for the de novo assembly and repair of photosystem II (PSII) in the chloroplast of Chlamydomonas reinhardtii, we used fluorescence in situ hybridization, immunofluorescence staining, and confocal microscopy. These locations were defined as having colocalized chloroplast mRNAs encoding PSII subunits and proteins of the chloroplast translation machinery specifically under conditions of PSII subunit synthesis. The results revealed that the synthesis of the D1 subunit for the repair of photodamaged PSII complexes occurs in regions of the chloroplast with thylakoids, consistent with the current model. However, for de novo PSII assembly, PSII subunit synthesis was detected in discrete regions near the pyrenoid, termed T zones (for translation zones). In two PSII assembly mutants, unassembled D1 subunits and incompletely assembled PSII complexes localized around the pyrenoid, where we propose that they mark an intermediate compartment of PSII assembly. These results reveal a novel chloroplast compartment that houses de novo PSII biogenesis and the regulated transport of newly assembled PSII complexes to thylakoid membranes throughout the chloroplast.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174875PMC
http://dx.doi.org/10.1105/tpc.107.054882DOI Listing

Publication Analysis

Top Keywords

psii complexes
12
psii assembly
12
psii
11
assembly repair
8
psii subunit
8
subunit synthesis
8
novo psii
8
assembled psii
8
chloroplast
7
photosystem assembly
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!