首页> 外文期刊>The Biochemical Journal >Molecular cloning, gene organization and expression of the human UDP-GalNAc : Neu5Ac alpha 2-3Gal beta-R beta l,4-N-acetylgalactosaminyltransferase responsible for the biosynthesis of the blood group Sd(a)/Cad antigen: evidence for an unusual extende
【24h】

Molecular cloning, gene organization and expression of the human UDP-GalNAc : Neu5Ac alpha 2-3Gal beta-R beta l,4-N-acetylgalactosaminyltransferase responsible for the biosynthesis of the blood group Sd(a)/Cad antigen: evidence for an unusual extende

机译:人UDP-GalNAc的分子克隆,基因组织和表达:负责血型Sd(a)/ Cad抗原生物合成的Neu5Ac alpha 2-3Gal beta-R beta 1,4-N-乙酰半乳糖胺基转移酶:证据表明存在异常延伸

获取原文
获取原文并翻译 | 示例
           

摘要

The human Sd(a) antigen is formed through the addition of an N-acetylgalactosamine residue via a beta1,4-linkage to a sub-terminal galactose residue substituted with an alpha2,3-linked sialic acid residue. We have taken advantage of the previously cloned mouse cDNA sequence of the UDP-GalNAc:Neu5Acalpha2-3Galbeta-R beta1,4-N-acetylgalactosaminyltransferase (Sd(a) beta1,4GalNAc transferase) to screen the human EST and genomic databases and to identify the corresponding human gene. The sequence spans over 35 kb of genomic DNA on chromosome 17 and comprises at least 12 exons. As judged by reverse transcription PCR, the human gene is expressed widely since it is detected in various amounts in almost all cell types studied. Northern blot analysis indicated that five Sd(a) beta1,4GalNAc transferase transcripts of 8.8, 6.1, 4.7, 3.8 and 1.65 kb were highly expressed in colon and to a lesser extent in kidney, stomach, ileum and rectum. The complete coding nucleotide sequence was amplified from Caco-2 cells. Interestingly, the alternative use of two first exons, named El(s) and El, leads to the production of two transcripts. These nucleotide sequences give rise potentially to two proteins of 506 and 566 amino acid residues, identical in their sequence with the exception of their cytoplasmic tail. The short form is highly similar (74 % identity) to the mouse enzyme whereas the long form shows an unusual long cytoplasmic tail of 66 amino acid residues that is as yet not described for any other mammalian glycosyltransferase. Upon transient transfection in Cos-7 cells of the common catalytic domain, a soluble form of the protein was obtained, which catalysed the transfer of GalNAc residues to alpha2,3-sialylated acceptor substrates, to form the GalNAcbeta1-4[Neu5Acalpha2-3]Gal 1-R trisaccharide common to both Sd(a) and Cad antigens. [References: 54]
机译:人的Sd(a)抗原是通过将β-,4-键的N-乙酰半乳糖胺残基添加到被α2,3-连接的唾液酸残基取代的亚末端半乳糖残基上而形成的。我们利用了先前克隆的UDP-GalNAc:Neu5Acalpha2-3Galbeta-R beta1,4-N-乙酰半乳糖胺基转移酶(Sd(a)beta1,4GalNAc转移酶)的小鼠cDNA序列来筛选人类EST和基因组数据库并进行鉴定相应的人类基因。该序列跨越17号染色​​体上超过35 kb的基因组DNA,并包含至少12个外显子。通过逆转录PCR判断,人基因广泛表达,因为在几乎所有研究的细胞类型中都以各种量检测到它。 Northern印迹分析表明,五个8.8、6.1、4.7、3.8和1.65 kb的Sd(a)beta1,4GalNAc转移酶转录本在结肠中高表达,而在肾脏,胃,回肠和直肠中表达程度较低。从Caco-2细胞扩增完整的编码核苷酸序列。有趣的是,两个第一个外显子,分别称为El(s)和El,的使用导致产生两个转录本。这些核苷酸序列潜在地产生两个506和566个氨基酸残基的蛋白质,除了其细胞质尾巴以外,它们的序列相同。短形式与小鼠酶高度相似(74%同一性),而长形式显示具有66个氨基酸残基的异常长的细胞质尾,这尚未针对任何其他哺乳动物糖基转移酶进行描述。在共同催化结构域的Cos-7细胞中进行瞬时转染后,获得了一种可溶形式的蛋白质,该蛋白质催化了GalNAc残基向alpha2,3-唾液酸化受体底物的转移,从而形成GalNAcbeta1-4 [Neu5Acalpha2-3] Sd(a)和Cad抗原共有的Gal 1-R三糖。 [参考:54]

著录项

相似文献

  • 外文文献
  • 专利
获取原文

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