Plant Cell Applied Biosystems SYBR(R) Cells-to-CT(TM) Kits
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Plant Cell Advance Online Publication
Published on November 30, 2007; 10.1105/tpc.107.054882


This Article
Right arrow Full Text - TPC Advance Online Pub. (PDF)
Right arrow Supplemental Data
Right arrow All Versions of this Article:
19/11/3640    most recent
tpc.107.054882v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Uniacke, J.
Right arrow Articles by Zerges, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Uniacke, J.
Right arrow Articles by Zerges, W.
Agricola
Right arrow Articles by Uniacke, J.
Right arrow Articles by Zerges, W.

Received August 8, 2007
Returned for revision November 7, 2007
Accepted November 8, 2007

Photosystem II Assembly and Repair Are Differentially Localized in Chlamydomonas

James Uniacke 1 and William Zerges 1*

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

* To whom correspondence should be addressed. E-mail: zerges{at}alcor.concordia.ca.

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.




This article has been cited by other articles:


Home page
Mol PlantHome page
W. Inwood, C. Yoshihara, R. Zalpuri, K.-S. Kim, and S. Kustu
The Ultrastructure of a Chlamydomonas reinhardtii Mutant Strain Lacking Phytoene Synthase Resembles that of a Colorless Alga
Mol Plant, September 19, 2008; (2008) ssn046v1.
[Abstract] [Full Text] [PDF]


Home page
JCBHome page
J. Uniacke and W. Zerges
Stress induces the assembly of RNA granules in the chloroplast of Chlamydomonas reinhardtii
J. Cell Biol., August 25, 2008; 182(4): 641 - 646.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
ASPB Publications THE PLANT CELL PLANT PHYSIOLOGY
Copyright © 2007 by the American Society of Plant Biologists