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First published online July 11, 2008; 10.1104/pp.108.123331

Plant Physiology 148:304-315 (2008)
© 2008 American Society of Plant Biologists

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ENVIRONMENTAL STRESS AND ADAPTATION TO STRESS

Overexpression of the Arabidopsis 10-Kilodalton Acyl-Coenzyme A-Binding Protein ACBP6 Enhances Freezing Tolerance1,[OA]

Qin-Fang Chen, Shi Xiao and Mee-Len Chye*

School of Biological Sciences, University of Hong Kong, Pokfulam, Hong Kong, China

Small 10-kD acyl-coenzyme A-binding proteins (ACBPs) are highly conserved proteins that are prevalent in eukaryotes. In Arabidopsis (Arabidopsis thaliana), other than the 10-kD ACBP homolog (designated Arabidopsis ACBP6), there are five larger forms of ACBPs ranging from 37.5 to 73.1 kD. In this study, the cytosolic subcellular localization of Arabidopsis ACBP6 was confirmed by analyses of transgenic Arabidopsis expressing autofluorescence-tagged ACBP6 and western-blot analysis of subcellular fractions using ACBP6-specific antibodies. The expression of Arabidopsis ACBP6 was noticeably induced at 48 h after 4°C treatment by northern-blot analysis and western-blot analysis. Furthermore, an acbp6 T-DNA insertional mutant that lacked ACBP6 mRNA and protein displayed increased sensitivity to freezing temperature (–8°C), while ACBP6-overexpressing transgenic Arabidopsis plants were conferred enhanced freezing tolerance. Northern-blot analysis indicated that ACBP6-associated freezing tolerance was not dependent on the induction of cold-regulated COLD-RESPONSIVE gene expression. Instead, ACBP6 overexpressors showed increased expression of mRNA encoding phospholipase D{delta}. Lipid profiling analyses of rosettes from cold-acclimated, freezing-treated (–8°C) transgenic Arabidopsis plants overexpressing ACBP6 showed a decline in phosphatidylcholine (–36% and –46%) and an elevation of phosphatidic acid (73% and 67%) in comparison with wild-type plants. From our comparison, the gain in freezing tolerance in ACBP6 overexpressors that was accompanied by decreases in phosphatidylcholine and an accumulation of phosphatidic acid is consistent with previous findings on phospholipase D{delta}-overexpressing transgenic Arabidopsis. In vitro filter-binding assays indicating that histidine-tagged ACBP6 binds phosphatidylcholine, but not phosphatidic acid or lysophosphatidylcholine, further imply a role for ACBP6 in phospholipid metabolism in Arabidopsis, including the possibility of ACBP6 in the cytosolic trafficking of phosphatidylcholine.


1 This work was supported by a Croucher Senior Research Fellowship awarded to M.-L.C. and by the University of Hong Kong (grant no. 10208034). Q.-F.C. and S.X. were supported by University of Hong Kong postgraduate studentships. The Kansas Lipidomics Research Center was supported by the National Science Foundation (grant nos. EPS 0236913, MCB 0455318, and DBI 0521587), the Kansas Technology Enterprise Corporation, the Kansas IDeA Network of Biomedical Research Excellence of the National Institutes of Health (grant no. P20RR16475), and Kansas State University.

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Mee-Len Chye (mlchye{at}hkucc.hku.hk).

[OA] Open Access articles can be viewed online without a subscription.

www.plantphysiol.org/cgi/doi/10.1104/pp.108.123331

* Corresponding author; e-mail mlchye{at}hkucc.hku.hk.

Received May 21, 2008; accepted July 6, 2008; published July 11, 2008.







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