Stoddart A, Zhang Y, Paige C J
The Wellesley Hospital Research Institute, University of Toronto, Ontario, Canada.
Nucleic Acids Res. 1996 Oct 15;24(20):4003-8. doi: 10.1093/nar/24.20.4003.
We describe the isolation of a cDNA encoding a murine sialic acid-specific 9-O-acetylesterase as well as its expression pattern in cells of both hematopoietic and non-hematopoietic origin. This enzyme catalyzes the removal of O-acetyl ester groups from position 9 of the parent sialic acid N-acetylneuraminic acid. The cDNA is 2105 nt in length and encodes a protein of 541 amino acids with a predicted molecular weight of 61 kDa, not including oligosaccharides linked to eight potential N-glycosylation sites. The cDNA encoding the acetylesterase displays a widespread distribution in various cell lines and tissues. Expression studies of B lineage cell lines and primary fetal liver cells revealed a developmentally regulated expression pattern in cells of hematopoietic origin. Given the importance of 9-O-acetylation of sialic acids, the cloning of the cDNA encoding a sialic acid-specific 9-O-acetylesterase will be helpful in understanding further the regulation of this post-translational modification and the biological consequences thereof.
我们描述了一种编码小鼠唾液酸特异性9-O-乙酰酯酶的cDNA的分离及其在造血和非造血来源细胞中的表达模式。这种酶催化从母体唾液酸N-乙酰神经氨酸的9位去除O-乙酰酯基团。该cDNA长度为2105 nt,编码一个由541个氨基酸组成的蛋白质,预测分子量为61 kDa,不包括与八个潜在N-糖基化位点相连的寡糖。编码乙酰酯酶的cDNA在各种细胞系和组织中广泛分布。对B系细胞系和原代胎肝细胞的表达研究揭示了造血来源细胞中受发育调控的表达模式。鉴于唾液酸9-O-乙酰化的重要性,编码唾液酸特异性9-O-乙酰酯酶的cDNA的克隆将有助于进一步理解这种翻译后修饰的调控及其生物学后果。