首页> 外文OA文献 >Molecular cloning of the cDNA encoding a murine sialic acid-specific 9-O-acetylesterase and RNA expression in cells of hematopoietic and non-hematopoietic origin.
【2h】

Molecular cloning of the cDNA encoding a murine sialic acid-specific 9-O-acetylesterase and RNA expression in cells of hematopoietic and non-hematopoietic origin.

机译:编码鼠唾液酸特异性9-O-乙酰酯酶的cDNA的分子克隆以及造血和非造血来源的细胞中的RNA表达。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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.
机译:我们描述了一种编码鼠唾液酸特异性9-O-乙酰酯酶的cDNA的分离及其在造血和非造血来源的细胞中的表达模式。该酶催化从亲本唾液酸N-乙酰神经氨酸的9位上除去O-乙酰酯基。 cDNA的长度为2105 nt,编码一个541个氨基酸的蛋白质,预测分子量为61 kDa,其中不包括与八个潜在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显示出广泛的分布。 B谱系细胞系和原代胎儿肝细胞的表达研究揭示了造血起源细胞中发育调控的表达模式。考虑到唾液酸的9-O-乙酰化的重要性,克隆编码唾液酸特异性9-O-乙酰基酯酶的cDNA将有助于进一步理解这种翻译后修饰的调控及其生物学结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号