This laboratory has previously identified a human gene encoding N-acetylglucosaminyltransferase I (GlcNAc-TI; EC 126.96.36.199) by complementation of the glycosylation defect in the Lec1 Chinese hamster ovary (CHO) cell mutant. A phage A library prepared from genomic DNA of a tertiary Lec1 transfectant (3°T) has now been used to obtain clones encoding an active GlcNAc-TI enzyme. A small genomic DNA fragment [≈4.6 kilobases (kb)], isolated from an Alu-positive λ clone, conferred human GlcNAc-TI activity upon transfection into Lec1 cells. An ≈1.3-kb probe generated from this DNA fragment detected unique but distinct DNA fragments in human and CHO genomic DNA. The probe also hybridized to a poly(A)+ RNA of ≈2.7 kb in human and CHO cells and allowed the isolation of a full-length cDNA encoding human GlcNAc-TI activity. The overall features of the cDNA and deduced protein sequence (445 amino acids) are typical of other Golgi transferases that are type II transmembrane proteins. Northern blot analysis with the same probe showed that Lec1 mutant cells also possessed an ≈2.7-kb poly(A)+ RNA, indicating that the lec1 mutation is a point mutation. (.
|Number of pages
|Proceedings of the National Academy of Sciences of the United States of America
|Published - 1990
- Cloning Golgi glycosyltransferase
- Gene rescue
- Genomic DNA transfection
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