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Plant Physiol, January 2003, Vol. 131, pp. 49-60
The Effects of Polyethylene Glycol on Gene Expression of
Developing White Spruce Somatic Embryos1,[w]
Claudio
Stasolla,2*
Leonel
van
Zyl,
Ulrika
Egertsdotter,
Deborah
Craig,
Wenbin
Liu, and
Ron R.
Sederoff
Forest Biotechnology Group, Department of Forestry, North Carolina
State University, Raleigh, North Carolina 27695-7247 (C.S., L.v.Z.,
D.C., W.L., R.R.S.); and Institute of Paper Science and
Technology, 500 10th Street NW, Atlanta, Georgia 30318 (U.E.)
Somatic embryogenic cultures of white spruce (Picea
glauca) represent a valuable system to study molecular
mechanisms regulating embryo development because many embryos of
defined developmental stages can be generated. The inclusion of
polyethylene glycol (PEG) in the maturation medium can improve the
number and quality of embryos produced. To learn more about the
mechanism of action of PEG, we analyzed transcript profiles of
stage-specific embryos matured without (control) or with (PEG treated)
PEG. RNA extracted from maturing spruce embryos was analyzed on DNA
microarrays containing 2,178 cDNAs from loblolly pine (Pinus
taeda). The efficiency of heterologous hybridization between
spruce and pine species on microarrays has been documented previously
(L. van Zyl, S. von Arnold, P. Bozhkov, Y. Chen, U. Egertsdotter, J. MacKay, R. Sederoff, J. Shen, L. Zelena, D. Clapham
[2002] Comp Funct Genomics 3: 306-318). Several pine genes,
including the apparent homologs to the Arabidopsis genes ZWILLE,
FIDDLEHEAD, FUSCA, and SCARECROW, increased in expression after PEG
treatments. These genes are known to be involved in the formation of
the embryo body plan and in the control of the shoot and root apical
meristems. The increased transcript levels of these genes in immature
PEG-treated embryos suggest that PEG may improve the quality of spruce
somatic embryos by promoting normal differentiation of the embryonic
shoot and root. Changes in the transcript levels of many genes involved
in sucrose catabolism and nitrogen assimilation and utilization were
also observed between control and PEG-treated embryos.
1
This work was supported by the Natural
Sciences and Engineering Research Council of Canada (fellowship to
C.S.), by the National Science Foundation (grant no. DBI-9975806 to
R.R.S.), and by the North Carolina State University Forest
Biotechnology Industrial Research Consortium.
2
Present address: Department of Biology,
University of Winnipeg, 515 Portage Avenue, Winnipeg, MB, Canada R3B 2E9.
[w]
The online version of this article contains Web-only
data. The supplemental material is available at www.plantphysiol.org.
*
Corresponding author; e-mail c.stasolla{at}uwinnipeg.ca; fax
204-774-4134.
© 2003 American Society of Plant Biologists
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