Blood group A glycosyltransferase occurring as alleles with high sequence difference is transiently induced during a Nippostrongylus brasiliensis parasite infection

被引:21
作者
Olson, FJ
Johansson, MEV
Klinga-Levan, K
Bouhours, D
Enerbäck, L
Hansson, GC
Karlsson, NG
机构
[1] Univ Gothenburg, Dept Biochem Med, SE-40530 Gothenburg, Sweden
[2] Univ Gothenburg, Dept Mol & Cell Biol, SE-40530 Gothenburg, Sweden
[3] Univ Nantes, Fac Med, INSERM, UMR 539,Unite Rech Biol & Physiopathol, F-44035 Nantes 1, France
[4] Univ Gothenburg, Sahlgrens Hosp, Dept Pathol, S-41345 Gothenburg, Sweden
关键词
D O I
10.1074/jbc.M112287200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neutral mucin oligosaccharides from the small intestine of control rats and rats infected with the parasite Nippostrongylus brasiliensis were released and analyzed by gas chromatography-mass spectrometry. Infected animals expressed seven blood group A-like structures that were all absent in the control animals. The blood group A nature of these epitopes was confirmed by blood group A reactivity of the prepared mucins, of which Muc2 was one. Transferase assays and Northern blotting on small intestines from infected animals showed that an alpha-N-acetylgalactosaminyltransferase similar to the human blood group A glycosyltransferase had been induced. The expression was a transient event, with a maximum at day 6 of the 13-day-long infection. The rat blood group A glycosyltransferase was cloned, revealing two forms with an amino acid similarity of 95%. Both types had blood group A transferase activity and were probably allelic because none of 12 analyzed inbred strains carried both types. The second type was found in outbred rats and in one inbred strain. First generation offspring of inbred rats of each type were heterozygous, further supporting the allelic hypothesis. The transient induction and the large allelic variation could suggest that glycosyltransferases are part of a dynamic system altering mucins and other glycoconjugates as a protecting mechanism against microbial challenges.
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收藏
页码:15044 / 15052
页数:9
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