The DC2.3 Gene in Caenorhabditis elegans Encodes a Galectin That Recognizes the Galactoseβ1→4Fucose Disaccharide Unit
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概要
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Galectins comprise a large family of β-galactoside-binding proteins in animals and fungi. We previously isolated cDNAs of 10 galectin and galectin-like genes (lec-1 to lec-6 and lec-8 to lec-11) from Caenorhabditis elegans and characterized the carbohydrate-binding properties of their recombinant proteins. In the present study, we isolated cDNA corresponding to an open reading frame of the DC2.3a gene from C. elegans total RNA; this cDNA encodes another potential galectin. A recombinant DC2.3a protein was expressed in Escherichia coli and used for analysis. The protein displayed hemagglutinating activity against rabbit erythrocytes, bound to an asialofetuin-Sepharose column, and was eluted with lactose. Furthermore, frontal affinity chromatography (FAC) analysis confirmed that DC2.3a recognized oligosaccharides with a non-reducing terminal galactose. According to these results, we designated DC2.3 as lec-12. The carbohydrate-binding property of the recombinant DC2.3a/LEC-12a was essentially similar to that of LEC-6. Additionally, DC2.3a/LEC-12a and LEC-6 showed higher affinities for the galactoseβ1→4fucose (Galβ1→4Fuc) disaccharide than for N-acetyllactosamine. This suggests that the principal recognition unit is the Galβ1→4Fuc disaccharide as in the case of the C. elegans galectins. However, the recombinant DC2.3a/LEC-12a showed weak affinity for N-glycan E3, which was previously shown to be a preferential endogenous ligand for LEC-6. The DC2.3a/LEC-12a endogenous ligand structures appear to be somewhat different but contain the same galactose-fucose recognition motif.
著者
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Kasai Ken-ichi
Department Of Biological Chemistry Faculty Of Pharmaceutical Sciences Teikyo University
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Nemoto-Sasaki Yoko
Department of Biological Chemistry, Teikyo University School of Pharmaceutical Sciences
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Arata Yoichiro
Department Of Biological Chemistry Faculty Of Pharmaceutical Sciences Teikyo University
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Nishiyama Kazusa
Laboratory of Synthetic Organic and Medicinal Chemistry, School of Pharmaceutical Sciences, Teikyo U
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Takahashi Hideyo
Laboratory of Synthetic Organic and Medicinal Chemistry, School of Pharmaceutical Sciences, Teikyo U
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Natsugari Hideaki
Laboratory of Synthetic Organic and Medicinal Chemistry, School of Pharmaceutical Sciences, Teikyo U
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Takeuchi Tomoharu
Department Of Biochemistry Graduate School Of Pharmaceutical Sciences Hokkaido University
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Takai Shunsuke
Department of Biological Chemistry, School of Pharmaceutical Sciences, Teikyo University
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Yamada Atsushi
Laboratory of Synthetic Organic and Medicinal Chemistry, School of Pharmaceutical Sciences, Teikyo U
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Yamada Atsushi
Laboratory of Synthetic Organic and Medicinal Chemistry, School of Pharmaceutical Sciences, Teikyo University
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Nemoto-Sasaki Yoko
Department of Biological Chemistry, School of Pharmaceutical Sciences, Teikyo University
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Arata Yoichiro
Department of Biological Chemistry, School of Pharmaceutical Sciences, Teikyo University
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Takeuchi Tomoharu
Department of Biological Chemistry, School of Pharmaceutical Sciences, Teikyo University
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