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Originally published In Press as doi:10.1074/jbc.M204183200 on May 20, 2002

J. Biol. Chem., Vol. 277, Issue 31, 27772-27781, August 2, 2002
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Purple Acid Phosphatases of Arabidopsis thaliana
COMPARATIVE ANALYSIS AND DIFFERENTIAL REGULATION BY PHOSPHATE DEPRIVATION*

Dongping LiDagger , Huifen ZhuDagger , Kunfan LiuDagger , Xin LiuDagger , Georg Leggewie§, Michael Udvardi§, and Daowen WangDagger

From the Dagger  Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China and the § Max Planck Institute of Molecular Plant Physiology, 14424 Potsdam, Germany

Purple acid phosphatases (PAPs) are members of the metallo-phosphoesterase family. They are characterized by the presence of seven conserved amino acid residues involved in coordinating the dimetal nuclear center in their reactive site. We compared the 29 PAPs predicted for Arabidopsis thaliana in their varieties of potential metal-ligating residues. Although 24 members possessed sets of metal-ligating residues typical of known PAPs, 1 member lacked four of the seven residues. For the remaining four members, potential metal-ligating residues were generally more similar to those in metal-dependent exonucleases and related proteins. Evidence was obtained for the expression of the majority of the 29 PAPs. To facilitate future investigations, a scheme for naming Arabidopsis PAPs and a system for classifying the 29 PAPs are proposed. The cDNA sequences and the responses to phosphate deprivation of seven Arabidopsis PAPs (AtPAP7-AtPAP13) were characterized. For some AtPAPs analyzed, there were fully processed transcripts as well as splice variants. The splice variants of AtPAP10 were found to associate with polyribosomes and may be translated into a NH2-terminal truncated protein. Phylogenetic investigations showed that AtPAPs 7 and 8, together with similar enzymes from other plant species, formed the low molecular weight plant PAP group. Members of this group were more closely related to PAPs from mammalian cells. AtPAPs 9-13, together with kidney bean PAP, formed the high molecular weight PAP group. In phosphate deprivation experiments, gene transcription of AtPAP11 and AtPAP12 was induced and increased, respectively, whereas that of the remaining five AtPAPs was not affected by phosphate deprivation. The present work demonstrates that structure variation and expression regulation of plant PAPs are more complex than previously described and provides a framework for comprehensive molecular genetic and biochemical studies of all Arabidopsis PAPs in the future.


* This work was supported by Grant J99-A-035 from the Ministry of Science and Technology of China and in part by a grant from the Max Planck Society of Germany.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EBI Data Bank with accession number(s) AF492659 (AtPAP7), AF492660 (AtPAP8), AF492661 (AtPAP9), AF492662 (AtPAP10), AF492663 (AtPAP11), AF492664 (AtPAP12), AF492665 (AtPAP13), AY090893 (AtPAP10 splice variant), and AY090894 (AtPAP13 splice variant).

To whom correspondence should be addressed. Tel.: 8610-64889380; Fax: 8610-64854467; E-mail: dwwang@genetics.ac.cn or daowenwang{at}hotmail.com.


Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.
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