Abeijon C, Robbins P W, Hirschberg C B
Department of Biochemistry and Molecular Biology, University of Massachusetts Medical Center, Worcester, 01655, USA.
Proc Natl Acad Sci U S A. 1996 Jun 11;93(12):5963-8. doi: 10.1073/pnas.93.12.5963.
The mannan chains of Kluyveromyces lactis mannoproteins are similar to those of Saccharomyces cerevisiae except that they lack mannose phosphate and have terminal alpha1-->2-linked N-acetylglucosamine. The biosynthesis of these chains probably occurs in the lumen of the Golgi apparatus, by analogy to S. cerevisiae. The sugar donors, GDP-mannose and UDP-GlcNAc, must first be transported from the cytosol, their site of synthesis, via specific Golgi membrane transporters into the lumen where they are substrates in the biosynthesis of these mannoproteins. A mutant of K. lactis, mnn2-2, that lacks terminal N-acetylglucosamine in its mannan chains in vivo, has recently been characterized and shown to have a specific defect in transport of UDP-GlcNAc into the lumen of Golgi vesicles in vitro. We have now cloned the gene encoding the K. lactis Golgi membrane UDP-GlcNAc transporter by complementation of the mnn2-2 mutation. The mnn2-2 mutant was transformed with a genomic library from wild-type K. lactis in a pKD1-derived vector; transformants were isolated and phenotypic correction was monitored following cell surface labeling with fluorescein isothiocyanate conjugated to Griffonia simplicifolia II lectin, which binds terminal N-acetylglucosamine, and a fluorescent activated cell sorter. A 2.4-kb DNA fragment was found to restore the wild-type lectin binding phenotype. Upon loss of the plasmid containing this fragment, reversion to the mutant phenotype occurred. The above fragment contained an open reading frame for a multitransmembrane spanning protein of 328 amino acids. The protein contains a leucine zipper motif and has high homology to predicted proteins from S. cerevisiae and C. elegans. In an assay in vitro, Golgi vesicles isolated from the transformant had regained their ability to transport UDP-GlcNAc. Taken together, the above results strongly suggest that the cloned gene encodes the Golgi UDP-GlcNAc transporter of K. lactis.
乳酸克鲁维酵母甘露糖蛋白的甘露聚糖链与酿酒酵母的相似,只是它们缺乏磷酸甘露糖且具有末端α1→2连接的N - 乙酰葡糖胺。类似于酿酒酵母,这些链的生物合成可能发生在高尔基体腔中。糖供体GDP - 甘露糖和UDP - GlcNAc必须首先从其合成部位胞质溶胶通过特定的高尔基体膜转运蛋白转运到腔内,在那里它们是这些甘露糖蛋白生物合成的底物。乳酸克鲁维酵母的一个突变体mnn2 - 2,其体内甘露聚糖链中缺乏末端N - 乙酰葡糖胺,最近已被鉴定,并显示在体外将UDP - GlcNAc转运到高尔基体小泡腔内存在特定缺陷。我们现在通过mnn2 - 2突变的互补克隆了编码乳酸克鲁维酵母高尔基体膜UDP - GlcNAc转运蛋白的基因。用来自野生型乳酸克鲁维酵母的基因组文库在pKD1衍生载体中转化mnn2 - 2突变体;分离转化体,并用与简单豆科凝集素II结合的异硫氰酸荧光素进行细胞表面标记,然后用荧光激活细胞分选仪监测表型校正。发现一个2.4kb的DNA片段恢复了野生型凝集素结合表型。当含有该片段的质粒丢失时,又恢复为突变体表型。上述片段包含一个328个氨基酸的多跨膜蛋白的开放阅读框。该蛋白含有亮氨酸拉链基序,与酿酒酵母和秀丽隐杆线虫预测的蛋白具有高度同源性。在体外试验中,从转化体分离得到的高尔基体小泡恢复了转运UDP - GlcNAc的能力。综上所述,上述结果强烈表明克隆的基因编码乳酸克鲁维酵母的高尔基体UDP - GlcNAc转运蛋白。