TY - JOUR
T1 - Localization and responsiveness of a cowpea apyrase VsNTPase1 to phytopathogenic microorganisms
AU - Takahashi, Hirotaka
AU - Toyoda, Kazuhiro
AU - Hirakawa, Yuzo
AU - Morishita, Kunihiko
AU - Kato, Toshiaki
AU - Inagaki, Yoshishige
AU - Ichinose, Yuki
AU - Shiraishi, Tomonori
N1 - Funding Information:
Acknowledgments We are grateful to Professor Yasuo Niwa, University of Shizuoka, Japan, for providing the sGFP (S65T) vector. This research was supported in part by grants from the Japan Society of the Promotion of Science (nos. 15108001 and 12052219) and by special coordination funds for the promotion of science and technology from the Japanese Ministry of Education, Culture, Sports, Science, and Technology. Financial support from Nippon Steel Co. Ltd., Chiba, Japan, and Sankyo Agro. Co. Ltd., Tokyo, Japan, is also acknowledged.
PY - 2006/6
Y1 - 2006/6
N2 - Apyrases (NTPases) are associated with both compatible and incompatible interactions between plants and microorganisms. Previously we reported that the ATPase activities of cell-wall-bound apyrases of several leguminous plants, such as pea, cowpea, soybean, and kidney bean, were enhanced by a glycoprotein elicitor and were inhibited in a species-specific manner by mucin-type glycopeptide suppressors secreted from a pea pathogenic fungus, Mycosphaerella pinodes. In this study, we isolated two apyrase genes, VsNTPase1 and VsNTPase2, from a cDNA library of Vigna sinensis Endl. cv. Sanjakusasage. Based on phylogenetic analysis, VsNTPase1 may belong to a group that responds to environmental stimuli. In a transient assay using DNA bombardment, a fusion protein of green fluorescent protein (GFP) and the N-terminal putative signal sequence of VsNTPase1 was distributed in the nucleus, cytoplasm (cytoskeletal structure), and cell wall. On the other hand, a fusion protein of GFP and the N-terminal putative VsNTPase2-signal sequence was localized in the cytoplasm, especially in small particles (perhaps mitochondria). A recombinant VsNTPase1 expressed in Spodoptera frugiperda 21 cells responded directly to signal molecules from several phytopathogenic microorganisms. Here, we discuss the role of apyrases in recognizing and responding to exogenous signals.
AB - Apyrases (NTPases) are associated with both compatible and incompatible interactions between plants and microorganisms. Previously we reported that the ATPase activities of cell-wall-bound apyrases of several leguminous plants, such as pea, cowpea, soybean, and kidney bean, were enhanced by a glycoprotein elicitor and were inhibited in a species-specific manner by mucin-type glycopeptide suppressors secreted from a pea pathogenic fungus, Mycosphaerella pinodes. In this study, we isolated two apyrase genes, VsNTPase1 and VsNTPase2, from a cDNA library of Vigna sinensis Endl. cv. Sanjakusasage. Based on phylogenetic analysis, VsNTPase1 may belong to a group that responds to environmental stimuli. In a transient assay using DNA bombardment, a fusion protein of green fluorescent protein (GFP) and the N-terminal putative signal sequence of VsNTPase1 was distributed in the nucleus, cytoplasm (cytoskeletal structure), and cell wall. On the other hand, a fusion protein of GFP and the N-terminal putative VsNTPase2-signal sequence was localized in the cytoplasm, especially in small particles (perhaps mitochondria). A recombinant VsNTPase1 expressed in Spodoptera frugiperda 21 cells responded directly to signal molecules from several phytopathogenic microorganisms. Here, we discuss the role of apyrases in recognizing and responding to exogenous signals.
KW - Apyrase
KW - Elicitor
KW - Mycosphaerella pinodes
KW - Suppressor
KW - Vigna sinensis Endl., cv. Sanjakusasage
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U2 - 10.1007/s10327-005-0267-3
DO - 10.1007/s10327-005-0267-3
M3 - Article
AN - SCOPUS:33744459210
SN - 1345-2630
VL - 72
SP - 143
EP - 151
JO - Journal of General Plant Pathology
JF - Journal of General Plant Pathology
IS - 3
ER -