Kukuruzinska M A, Robbins P W
Proc Natl Acad Sci U S A. 1987 Apr;84(8):2145-9. doi: 10.1073/pnas.84.8.2145.
The first enzyme in the lipid-linked oligosaccharide biosynthetic pathway, UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (UDP-N-acetyl-D-glucosamine:dolichyl-phosphate-N-acetyl- D-glucosaminephosphotransferase, EC 2.7.8.15), is encoded by the ALG7 gene. We show that this gene is essential for cell growth, since a null mutation constructed with standard gene disruption techniques results in cell lethality. The ALG7 gene is transcribed into two major messages, approximately 1.38 and 1.56 kilobase pairs (kbp) in size, and this heterogeneity has been mapped to the 3' untranslated region. Two sets of tripartite sequences implicated in transcription termination begin 15 bp and 256 bp past the translation stop codon, TGA. The ratios of the two major transcripts change with gene dosage, with the longer mRNA becoming more abundant in cells containing higher levels of the ALG7 gene. Changes in transcript ratios are also observed in mutants defective in lipid-linked sugar-donor biosynthesis. In addition, there is 5' heterogeneity in the ALG7 mRNAs. The transcripts start at four initiation sites located within a 20-bp region. Two potentially functional TATA elements have been identified at positions -157 and -139, which may be involved in initiation from multiple sites. These features point to numerous factors that may be involved in the regulation of the expression of the ALG7 gene.
脂质连接寡糖生物合成途径中的第一个酶,UDP-N-乙酰葡糖胺-多萜醇磷酸-N-乙酰葡糖胺磷酸转移酶(UDP-N-乙酰-D-葡糖胺:多萜醇磷酸-N-乙酰-D-葡糖胺磷酸转移酶,EC 2.7.8.15),由ALG7基因编码。我们发现该基因对细胞生长至关重要,因为用标准基因破坏技术构建的无效突变会导致细胞死亡。ALG7基因转录为两条主要的mRNA,大小约为1.38和1.56千碱基对(kbp),这种异质性已定位到3'非翻译区。两组与转录终止有关的三联体序列在翻译终止密码子TGA下游15 bp和256 bp处开始。两种主要转录本的比例随基因剂量而变化,在含有较高水平ALG7基因的细胞中,较长的mRNA更为丰富。在脂质连接糖供体生物合成缺陷的突变体中也观察到转录本比例的变化。此外,ALG7 mRNA存在5'端异质性。转录本从位于20 bp区域内的四个起始位点开始。在-157和-139位置已鉴定出两个潜在的功能性TATA元件,它们可能参与多个位点的起始。这些特征表明可能有许多因素参与ALG7基因表达的调控。