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用人类DNA转染后小鼠细胞中血型H抗原决定簇和GDP-L-岩藻糖:β-D-半乳糖苷2-α-L-岩藻糖基转移酶的稳定表达。

Stable expression of blood group H determinants and GDP-L-fucose: beta-D-galactoside 2-alpha-L-fucosyltransferase in mouse cells after transfection with human DNA.

作者信息

Ernst L K, Rajan V P, Larsen R D, Ruff M M, Lowe J B

机构信息

Howard Hughes Medical Institute, University of Michigan Medical School, Ann Arbor 48109-0650.

出版信息

J Biol Chem. 1989 Feb 25;264(6):3436-47.

PMID:2464598
Abstract

We report here the application of a genetic approach to identify and isolate human DNA sequences controlling the expression of a GDP-L-fucose: beta-D-galactoside 2-alpha-L-fucosyltransferase [alpha-1,2)fucosyltransferase). Mouse L cells were chosen as host cells for this scheme since they express the necessary substrate and acceptor molecules for surface display of blood group H Fuc alpha 1----2 G al linkages constructed by (alpha-1,2) fucosyltransferases. However, they do not express cell surface blood group H structures nor detectable (alpha-1,2)fucosyltransferase activity. We therefore asked if (alpha-1,2)fucosyltransferase activity could be expressed and detected in these cells after transfection with human DNA sequences. These cells were transfected with genomic DNA isolated from a human cell line (A431) that expresses (alpha-1,2)fucosyltransferase. A panning procedure and fluorescence-activated cell sorting were used to isolate a mouse transfectant cell line that expresses cell surface H Fuc alpha 1----2 Gal linkages and a cognate (alpha-1,2)fucosyltransferase. Southern blot analysis showed that the genome of this cell line contains several hundred kilobase pairs of human DNA. Genomic DNA from this primary transfectant was used to transfect mouse L cells, and several independent, H-expressing secondary transfectants were isolated by immunological selection. Each expresses an (alpha-1,2)fucosyltransferase. Southern blot analysis demonstrated that the genome of each secondary transfectant contains common, characteristic human DNA restriction fragments. These results show that transfected human DNA sequences determine expression of the (alpha-1,2)fucosyltransferases in the mouse transfectants, that these sequences represent a single locus, and that they are within or linked to specific human restriction fragments identifiable in each secondary transfectant. These sequences may represent a human (alpha-1,2)fucosyltransferase gene.

摘要

我们在此报告一种遗传学方法的应用,该方法用于鉴定和分离控制GDP-L-岩藻糖:β-D-半乳糖苷2-α-L-岩藻糖基转移酶([α-1,2]岩藻糖基转移酶)表达的人类DNA序列。选择小鼠L细胞作为该方案的宿主细胞,因为它们表达通过(α-1,2)岩藻糖基转移酶构建的血型H Fucα1----2 Gal连接在表面展示所需的底物和受体分子。然而,它们不表达细胞表面血型H结构,也没有可检测到的(α-1,2)岩藻糖基转移酶活性。因此,我们询问在用人类DNA序列转染这些细胞后,(α-1,2)岩藻糖基转移酶活性是否能在这些细胞中表达并被检测到。用从表达(α-1,2)岩藻糖基转移酶的人类细胞系(A431)分离的基因组DNA转染这些细胞。采用淘选程序和荧光激活细胞分选来分离表达细胞表面H Fucα1----2 Gal连接和同源(α-1,2)岩藻糖基转移酶的小鼠转染细胞系。Southern印迹分析表明,该细胞系的基因组包含数百千碱基对的人类DNA。来自该原代转染细胞的基因组DNA用于转染小鼠L细胞,并通过免疫选择分离出几个独立的、表达H的二代转染细胞。每个细胞都表达一种(α-1,2)岩藻糖基转移酶。Southern印迹分析表明,每个二代转染细胞的基因组都包含共同的、特征性的人类DNA限制性片段。这些结果表明,转染的人类DNA序列决定了小鼠转染细胞中(α-1,2)岩藻糖基转移酶的表达,这些序列代表一个单一基因座,并且它们位于每个二代转染细胞中可识别的特定人类限制性片段内或与之相连。这些序列可能代表一个人类(α-1,2)岩藻糖基转移酶基因。

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