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Activity and tissue distribution of splice variants of alpha6-fucosyltransferase in human embryogenesis.

机译:人胚发生中α6-岩藻糖基转移酶剪接变体的活性和组织分布。

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The product of the FUT8 gene transfers an alpha1-6 fucose on the innermost N-acetylglucosamine of the chitobiose core of N-glycans. Northern blot analysis shows four main transcripts of 3.0, 3.3, 3.9, and 4.2 kb in the embryo. The larger forms around 4-kb decrease in fetus and adult. Fourteen embryo transcripts of FUT8 were cloned. Twelve exons comprising two new 5'untranslated-exons (A and B) and two new 3'UT-ends (L1 and L2) and the complete genomic organization of the FUT8 gene (330 kb) are described. Transcripts starting with the 5'UT-exon A are always associated with exons C and D. Exon B initiates another series of transcripts associated to exon C and D or directly to exon D. A third series of transcripts starts at exon C. The data suggest an expression of FUT8 regulated by three different promoters, starting transcription in exons A, B, or C. The A or C series are better expressed than the B series. After transfection with these cDNA constructs the transcripts with 5'UT-exons A or C have higher expression of FUT8 transcripts and higher alpha6-fucosyltransferase activity, whereas the activity of the B series is about two-thirds lower for both parameters, suggesting that exon B reduces the expression of the transcripts.
机译:FUT8基因的产物将α1-6岩藻糖转移到N-聚糖的壳二糖核心的最里面的N-乙酰氨基葡萄糖上。 Northern印迹分析显示了胚胎中3.0、3.3、3.9和4.2 kb的四个主要转录物。大约4kb的较大形式在胎儿和成人中减少。克隆了14个FUT8的胚胎转录物。描述了十二个外显子,包括两个新的5'非翻译外显子(A和B)和两个新的3'UT末端(L1和L2)以及FUT8基因的完整基因组组织(330 kb)。以5'UT外显子A开头的转录本始终与外显子C和D相关联。外显子B引发与外显子C和D或直接与外显子D相关的另一系列转录本。第三组转录本始于外显子C.数据提示由三个不同启动子调节的FUT8的表达,在外显子A,B或C中开始转录。A或C系列的表达优于B系列。用这些cDNA构建体转染后,具有5'UT外显子A或C的转录本具有较高的FUT8转录本表达和较高的α6-岩藻糖基转移酶活性,而B系列的两个参数的活性均低约三分之二,这表明外显子B减少了转录物的表达。

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