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Originally published In Press as doi:10.1074/jbc.M609866200 on March 23, 2007
J. Biol. Chem., Vol. 282, Issue 21, 15619-15631, May 25, 2007
Oxygen Initiation of Respiration and Mitochondrial Biogenesis in Rice*
Katharine A. Howell,
Kim Cheng,
Monika W. Murcha,
Linne E. Jenkin,
A. Harvey Millar1, and
James Whelan2
From the
Australian Research Council Centre of Excellence in Plant Energy Biology, University of Western Australia, Perth, Western Australia 6009, Australia
Rice growth under aerobic and anaerobic conditions allowed aspects of mitochondrial biogenesis to be identified as dependent on or independent of an oxygen signal. Analysis of transcripts encoding mitochondrial components found that a subset of these genes respond to oxygen (defined as aerobic), whereas others are relatively unaffected by oxygen availability. Mitochondria formed during growth in anaerobic conditions had reduced protein levels of tricarboxylic acid cycle components and cytochrome-containing complexes of the respiratory chain and repressed respiratory functionality. In general, the capacity of the general import pathway was found to be significantly lower in mitochondria isolated from tissue grown under anaerobic conditions, whereas the carrier import pathway capacity was not affected by changes in oxygen availability. Transcript levels of genes encoding components of the protein import apparatus were generally not affected by the absence of oxygen, and their protein abundance was severalfold higher in mitochondria isolated from anaerobically grown tissue. However, both transcript and protein abundances of the subunits of the mitochondrial processing peptidase, which in plants is integrated into the cytochrome bc1 complex, were repressed under anaerobic conditions. Therefore, in this system, an increase in import capacity is correlated with an increase in the abundance of the cytochrome bc1 complex, which is ultimately dependent on the presence of oxygen, providing a link between the respiratory chain and protein import apparatus.
Received for publication, October 20, 2006
, and in revised form, March 22, 2007.
* This work was supported by funding to the Australian Research Council Centre of Excellence in Plant Energy Biology. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
The on-line version of this article (available at http://www.jbc.org) contains supplemental Figs. 1 and 2.
1 Supported by an Australian Research Council Australian Professorial Fellowship.
2 To whom correspondence should be addressed: ARC Centre of Excellence in Plant Energy Biology, M316 MCS Bldg., University of Western Australia, 35 Stirling Hwy., Crawley, Perth 6009, Australia. Tel.: 61-8-6488-1749; Fax: 61-8-6488-4401; E-mail: seamus{at}cyllene.uwa.edu.au.

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Copyright © 2007 by the American Society for Biochemistry and Molecular Biology.
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