Díaz M, Sanchez Y, Bennett T, Sun C R, Godoy C, Tamanoi F, Duran A, Perez P
Instituto de Microbiología Bioquímica, Consejo Superior de Investigaciones Científicas, Salamanca, Spain.
EMBO J. 1993 Dec 15;12(13):5245-54. doi: 10.1002/j.1460-2075.1993.tb06220.x.
The product of the Schizosaccharomyces pombe cwg2+ gene is involved in the biosynthesis of beta-D-glucan. When grown at the non-permissive temperature, cwg2-1 mutant cells lyse in the absence of an osmotic stabilizer and display a reduced (1-3) beta-D-glucan content and (1-3) beta-D-glucan synthase activity. The cwg2+ gene was cloned by the rescue of the cwg2-1 mutant phenotype using an S. pombe genomic library and subsequently verified by integration of the appropriate insert into the S. pombe genome. Determination of the nucleotide sequence of this gene revealed a putative open reading frame of 1065 bp encoding a polypeptide of 355 amino acids with a calculated M(r) of 40,019. The cwg2+ DNA hybridizes to a main transcript, the 5' end of which maps to a position 469 bp upstream of the predicted start of translation. The sequence between the transcription and the translation start sites is unusually long and has several short open reading frames which suggest a translational control of the gene expression. Comparative analysis of the predicted amino acid sequence shows that it possesses significant similarity to three Saccharomyces cerevisiae proteins, encoded by the DPR1/RAM1, CDC43/CAL1 and ORF2/BET2 genes respectively, which are beta subunits of different prenyltransferases. When grown at 37 degrees C, cwg2-1 mutant extracts were specifically deficient in geranylgeranyltransferase type I activity, as measured in vitro. Multiple copies of the CDC43 gene can partially suppress the growth and (1-3) beta-D-glucan synthase defect of the cwg2-1 mutant at the restrictive temperature. In a similar manner, the cwg2+ gene can partially suppress the cdc43-2 growth defect. These results indicate that cwg2+ is the structural gene for the beta subunit of geranylgeranyltransferase type I in S. pombe and that this enzyme is required for (1-3) beta-D-glucan synthase activity. The functional homology of Cwg2 with Cdc43, which has been implicated in the control of cell polarity, suggests a link between two morphogenetic events such as establishment of cell polarity and cell wall biosynthesis.
粟酒裂殖酵母cwg2+基因的产物参与β-D-葡聚糖的生物合成。当在非允许温度下生长时,cwg2-1突变细胞在没有渗透稳定剂的情况下会裂解,并且显示出降低的(1-3)β-D-葡聚糖含量和(1-3)β-D-葡聚糖合酶活性。通过使用粟酒裂殖酵母基因组文库挽救cwg2-1突变体表型来克隆cwg2+基因,随后通过将合适的插入片段整合到粟酒裂殖酵母基因组中进行验证。对该基因核苷酸序列的测定揭示了一个1065 bp的推定开放阅读框,编码一个355个氨基酸的多肽,计算的M(r)为40,019。cwg2+ DNA与一个主要转录本杂交,其5'端定位于预测翻译起始点上游469 bp的位置。转录起始位点和翻译起始位点之间的序列异常长,并且有几个短的开放阅读框,这表明该基因表达存在翻译控制。对预测氨基酸序列的比较分析表明,它与分别由DPR1/RAM1、CDC43/CAL1和ORF2/BET2基因编码的三种酿酒酵母蛋白具有显著相似性,这些蛋白是不同异戊二烯基转移酶的β亚基。当在37℃下生长时,体外测定显示cwg2-1突变提取物在I型香叶基香叶基转移酶活性方面存在特异性缺陷。CDC43基因的多个拷贝可以部分抑制cwg2-1突变体在限制温度下的生长和(1-3)β-D-葡聚糖合酶缺陷。以类似的方式,cwg2+基因可以部分抑制cdc43-2生长缺陷。这些结果表明,cwg2+是粟酒裂殖酵母中I型香叶基香叶基转移酶β亚基的结构基因,并且该酶是(1-3)β-D-葡聚糖合酶活性所必需的。Cwg2与Cdc43的功能同源性,后者与细胞极性的控制有关,表明细胞极性建立和细胞壁生物合成等两个形态发生事件之间存在联系。