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Plant Physiology 135:1314-1323 (2004)
© 2004 American Society of Plant Biologists

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BIOCHEMICAL PROCESSES AND MACROMOLECULAR STRUCTURES

Characterization of Arabidopsis Glutamine Phosphoribosyl Pyrophosphate Amidotransferase-Deficient Mutants1

Wei-Fon Hung, Lih-Jen Chen, Ralf Boldt, Chih-Wen Sun2 and Hsou-min Li*

Graduate Institute of Life Sciences, National Defense Medical Center, Taipei 114, Taiwan (W.-F.H.); Institute of Molecular Biology, Academia Sinica, Taipei 115, Taiwan (W.-F.H., L.-J.C., C.-W.S., H.-m.L.); and Department of Plant Physiology, University of Rostock, 18051 Rostock, Germany (R.B.)

Using a transgene-based screening, we previously isolated several Arabidopsis mutants defective in protein import into chloroplasts. Positional cloning of one of the loci, CIA1, revealed that CIA1 encodes Gln phosphoribosyl pyrophosphate amidotransferase 2 (ATase2), one of the three ATase isozymes responsible for the first committed step of de novo purine biosynthesis. The cia1 mutant had normal green cotyledons but small and albino/pale-green mosaic leaves. Adding AMP, but not cytokinin or NADH, to plant liquid cultures partially complemented the mutant phenotypes. Both ATase1 and ATase2 were localized to chloroplasts. Overexpression of ATase1 fully complemented the ATase2-deficient phenotypes. A T-DNA insertion knockout mutant of the ATase1 gene was also obtained. The mutant was indistinguishable from the wild type. A double mutant of cia1/ATase1-knockout had the same phenotype as cia1, suggesting at least partial gene redundancy between ATase1 and ATase2. Characterizations of the cia1 mutant revealed that mutant leaves had slightly smaller cell size but only half the cell number of wild-type leaves. This phenotype confirms the role of de novo purine biosynthesis in cell division. Chloroplasts isolated from the cia1 mutant imported proteins at an efficiency less than 50% that of wild-type chloroplasts. Adding ATP and GTP to isolated mutant chloroplasts could not restore the import efficiency. We conclude that de novo purine biosynthesis is not only important for cell division, but also for chloroplast biogenesis.


1 This work was supported by grants from the National Science Council (NSC 90–2321–B001–006) and the Academia Sinica of Taiwan (to H.-m.L.), and from the Deutsche Forschungsgemeinschaft (BO 1236/3–1 to R.B.) as part of the The Arabidopsis Functional Genomics Network (AFGN).

2 Present address: Department of Life Sciences, National Normal University, Taipei 116, Taiwan.

Article, publication date, and citation information can be found at www.plantphysiol.org/cgi/doi/10.1104/pp.104.040956.

* Corresponding author; e-mail mbhmli{at}ccvax.sinica.edu.tw; fax 886–2–2782–6085.

Received February 14, 2004; returned for revision May 3, 2004; accepted May 6, 2004.




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