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首页> 外文期刊>Glycoconjugate Journal >Molecular characterization of pig α2,3-Gal-β1,3-GalNAc-α2,6-sialyltransferase (pST6GalNAc IV) gene specific for Neu5Acα2-3Galβ1-3GalNAc trisaccharide structure
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Molecular characterization of pig α2,3-Gal-β1,3-GalNAc-α2,6-sialyltransferase (pST6GalNAc IV) gene specific for Neu5Acα2-3Galβ1-3GalNAc trisaccharide structure

机译:Neu5Acα2-3Galβ1-3GalNAc三糖结构特异的猪α2,3-Gal-β1,3-GalNAc-α2,6-唾液酸转移酶(pST6GalNAc IV)基因的分子特征

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摘要

Sialic acids of glycoconjugates play crucial roles in various biological processes, such as cell-cell communication and cell-substrate interaction. A sisalyltransferase, ST6GalNAc IV (Neu5Ac-α2,3-Gal-β1,3-GalNAc-α2,6-sialyltransferase), catalyzes the formation of α2-6-linkages onto GalNAc residues of O-glycosidically linked Ser/Thr of proteins. In this study, we cloned the pig ST6GalNAc IV (pST6GalNAc IV) and investigated its functional characterization. pST6GalNAc IV cDNA has been isolated from pig liver tissues and it contains an entire open reading frame (ORF, 906 bp) coding for 302 amino acid residues. Entire ORF of pST6GalNAc IV containing sialylmotif ‘L’—(Large), ‘S’—(Small) and ‘—VS’ (Very small) has a high degree of sequence similarity with Homo sapiens (90%), Pan troglodytes (91%) and Mus musculus (87%). Expression of pST6GalNAc IV mRNA in various pig tissues was identified by reverse transcription polymerase chain reaction (RT-PCR) analysis. pST6GalNAc IV mRNA was highly expressed in tongue, muscle and heart, whereas it was not expressed in pancreas. For functional characterization of pST6GalNAc IV gene in pig kidney PK15 cells, we have also established pST6GalNAc IV-transfected PK15 cells, which are stably expressing the pST6GalNAc IV gene. The glycosylation pattern of pST6GalNAc IV-transfected PK15 cells was detected by flow cytometry and immunofluorescence analysis with Maackia amurensis agglutinin (MAA), Maackia amurensis hemagglutinin (MAL II), Sambucus nigra agglutinin (SNA) and peanut agglutinin (PNA) lectins. The specific carbohydrate structures of Neu5Acα2-3Galβ1-3(Neu5Acα2-6)GalNAc tetrasaccharide or Neu5Acα2-6GalNAc disaccharide recognized by MAL-II and SNA were revealed to be newly synthesized by pST6GalNAc IV. From the results, it was suggested that the pig pST6GalNAc IV gene is capable of synthesizing Neu5Acα2-3Galβ1-3(Neu5Acα2-6)GalNAc tetrasaccharide structures on O-glycoproteins.
机译:糖缀合物的唾液酸在各种生物学过程中起着至关重要的作用,例如细胞间的通讯和细胞与底物的相互作用。剑麻酰转移酶ST6GalNAc IV(Neu5Ac-α2,3-Gal-β1,3-GalNAc-α2,6-唾液酸转移酶)催化α2-键连接到O-糖苷键连接的蛋白质Ser / Thr的GalNAc残基上。在这项研究中,我们克隆了猪ST6GalNAc IV(pST6GalNAc IV),并研究了其功能特性。从猪肝组织中分离出pST6GalNAc IV cDNA,它包含一个完整的开放阅读框(ORF,906 bp),编码302个氨基酸残基。包含唾液酸基序'L'-(大),'S'-(小)和'-VS'(非常小)的pST6GalNAc IV的整个ORF与智人(90%),泛虫(91)具有高度的序列相似性%)和小家鼠(87%)。通过逆转录聚合酶链反应(RT-PCR)分析鉴定了pST6GalNAc IV mRNA在各种猪组织中的表达。 pST6GalNAc IV mRNA在舌,肌肉和心脏中高表达,而在胰腺中不表达。为了在猪肾PK15细胞中鉴定pST6GalNAc IV基因的功能,我们还建立了pST6GalNAc IV转染的PK15细胞,该细胞稳定表达pST6GalNAc IV基因。通过流式细胞术和免疫荧光分析,用黑莓黑胶凝集素(MAA),黑莓黑血球凝集素(MAL II),黑接骨木素凝集素(SNA)和花生凝集素(PNA)凝集素检测pST6GalNAc IV转染的PK15细胞的糖基化模式。通过pST6GalNAc IV新发现了被MAL-II和SNA识别的Neu5Acα2-3Galβ1-3(Neu5Acα2-6)GalNAc四糖或Neu5Acα2-6GalNAc二糖的特定碳水化合物结构。从结果表明,猪pST6GalNAc IV基因能够在O-糖蛋白上合成Neu5Acα2-3Galβ1-3(Neu5Acα2-6)GalNAc四糖结构。

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