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Plant Physiol, September 2001, Vol. 127, pp. 131-141
Targeting a Nuclear Anthranilate Synthase -Subunit Gene to the
Tobacco Plastid Genome Results in Enhanced Tryptophan Biosynthesis.
Return of a Gene to Its Pre-Endosymbiotic
Origin1
Xing-Hai
Zhang,
Jeffrey E.
Brotherton,
Jack M.
Widholm, and
Archie
R.
Portis Jr.*
Photosynthesis Research Unit, United States Department of
Agriculture-Agricultural Research Service (X.-H.Z., A.R.P.), and
Department of Crop Sciences (X.-H.Z., J.E.B., J.M.W., A.R.P.),
University of Illinois, Urbana, Illinois 61801
Anthranilate synthase (AS), the control enzyme of the tryptophan
(Trp) biosynthetic pathway, is encoded by nuclear genes, but is
transported into the plastids. A tobacco (Nicotiana
tabacum) cDNA (ASA2) encoding a
feedback-insensitive tobacco AS -subunit was transformed into two
different sites of the tobacco plastid genome through site-specific
insertion to obtain transplastomic plants with normal phenotype and
fertility. A high and uniform level of ASA2 mRNA was
observed in the transplastomic plants but not in the wild type.
Although the plants with the transgene insertion at
ndhF-trnL only expressed one size of the
ASA2 mRNA, the plants with the transgene incorporated
into the region between accD and open reading frame
(ORF) 184 exhibited two species of mRNA, apparently due to
readthrough. The transplastomic plants exhibited a higher level of AS
-subunit protein and AS enzyme activity that was less sensitive to
Trp-feedback inhibition, leading to greatly increased free Trp levels
in leaves and total Trp levels in seeds. Resistance to an AS inhibitor,
5-methyl-Trp, was found during seed germination and in suspension
cultures of the transplastomic plants. The resistance to the selection
agent spectinomycin and to 5-methyl-Trp was transmitted maternally.
These results demonstrate the feasibility of modifying the biosynthetic
pathways of important metabolites through transformation of the plastid
genome by relocating a native gene from the nucleus to the plastid
genome. Very high and uniform levels of gene expression can be observed
in different lines, probably due to the identical insertion sites, in
contrast to nuclear transformation where random insertions occur.
1
This work was supported by the Illinois Soybean
Program Operating Board, by the Illinois Agricultural Experiment
Station, and by the U.S. Department of Agriculture.
*
Corresponding author; e-mail arportis{at}uiuc.edu; fax
217-244-4419.
© 2001 American Society of Plant Physiologists
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