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Comparative Study
. 2003 May;132(1):230-42.
doi: 10.1104/pp.102.018986.

Towards an analysis of the rice mitochondrial proteome

Affiliations
Comparative Study

Towards an analysis of the rice mitochondrial proteome

Joshua L Heazlewood et al. Plant Physiol. 2003 May.

Abstract

Purified rice (Oryza sativa) mitochondrial proteins have been arrayed by isoelectric focusing/polyacrylamide gel electrophoresis (PAGE), by blue-native (BN) PAGE, and by reverse-phase high-performance liquid chromatography (LC) separation (LC-mass spectrometry [MS]). From these protein arrays, we have identified a range of rice mitochondrial proteins, including hydrophilic/hydrophobic proteins (grand average of hydropathicity = -1.27 to +0.84), highly basic and acid proteins (isoelectric point = 4.0-12.5), and proteins over a large molecular mass range (6.7-252 kD), using proteomic approaches. BN PAGE provided a detailed picture of electron transport chain protein complexes. A total of 232 protein spots from isoelectric focusing/PAGE and BN PAGE separations were excised, trypsin digested, and analyzed by tandem MS (MS/MS). Using this dataset, 149 of the protein spots (the products of 91 nonredundant genes) were identified by searching translated rice open reading frames from genomic sequence and six-frame translated rice expressed sequence tags. Sequence comparison allowed us to assign functions to a subset of 85 proteins, including many of the major function categories expected for this organelle. A further six spots were matched to rice sequences for which no specific function has yet been determined. Complete digestion of mitochondrial proteins with trypsin yielded a peptide mixture that was analyzed directly by reverse-phase LC via organic solvent elution from a C-18 column (LC-MS). These data yielded 170 MS/MS spectra that matched 72 sequence entries from open reading frame and expressed sequence tag databases. Forty-five of these were obtained using LC-MS alone, whereas 28 proteins were identified by both LC-MS and gel-based separations. In total, 136 nonredundant rice proteins were identified, including a new set of 23 proteins of unknown function located in plant mitochondria. We also report the first direct identification, to our knowledge, of PPR (pentatricopeptide repeat) proteins in the plant mitochondrial proteome. This dataset provides the first extensive picture, to our knowledge, of mitochondrial functions in a model monocot plant.

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Figures

Figure 1
Figure 1
IEF/SDS-PAGE separation of rice mitochondrial proteins (pI = 3–10). A total of 145 protein spots from this map were excised, digested, and analyzed by MS/MS. Eighty were identified, and these are numbered for comparison with text and Table II. Numbers on the horizontal axis are pI, and numbers on the vertical axis are apparent molecular mass (in kilodaltons).
Figure 2
Figure 2
BN SDS-PAGE separation of rice membrane mitochondrial proteins. A total of 89 protein spots from this map were excised, digested, and analyzed by MS/MS. Fifty-seven were identified, and these are numbered for comparison with text and Table II. Numbers on vertical axis are apparent molecular mass of protein subunits (kilodaltons), and annotations on horizontal axis are known mitochondrial protein complexes identified in this study.
Figure 3
Figure 3
Comparison of identified rice protein sets. Proportion of rice proteins identified by the three separation techniques (IEF/SDS-PAGE, clear; BN SDS-PAGE, gray; and LC-MS, black) in different classes of hydrophobicity (A), molecular mass (B), and pI (C). D, Overlapping of targeting prediction of the rice proteins identified by TargetP, Predotar, and MitoProtII. Numbers in each circle indicate numbers predicted either by one, two, or all three predictors.

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References

    1. Arabidopsis Genome Initiative. Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. Nature. 2000;408:796–815. - PubMed
    1. Atkins CA, Smith PMC, Storer PJ. Re-examination of the intracellular localisation of de novo purine synthesis in cowpea nodules. Plant Physiol. 1997;113:127–135. - PMC - PubMed
    1. Bardel J, Louwagie M, Jaquinod M, Jourdain A, Luche S, Rabilloud T, Macherel D, Garin J, Bourguignon J. A survey of the plant mitochondrial proteome in relation to development. Proteomics. 2002;2:880–898. - PubMed
    1. Bartoli C, Pastori G, Foyer C. Ascorbate biosynthesis in mitochondria is linked to the electron transport chain between complexes III and IV. Plant Physiol. 2000;123:335–343. - PMC - PubMed
    1. Bentolila S, Alfonso AA, Hanson MR. A pentatricopeptide repeat-containing gene restores fertility to cytoplasmic male-sterile plants. Proc Natl Acad Sci USA. 2002;99:10887–10892. - PMC - PubMed

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