Yokoyama K, Saitoh S, Ishida M, Yamakawa Y, Nakamura K, Inoue K, Taguchi R, Tokumura A, Nishijima M, Yanagida M, Setaka M
Faculty of Pharmaceutical Sciences, Teikyo University, Sagamiko, Kanagawa, Japan.
Biochim Biophys Acta. 2001 Jun 29;1532(3):223-33. doi: 10.1016/s1388-1981(01)00134-2.
Fission yeast lsd1 strains show aberrant mitosis with a lsd phenotype, large and small daughter nuclei, and a very thick septum, the phenotypic expression being temperature-sensitive. The lsd1(+) gene is the homologue of the budding yeast FAS2 gene encoding the fatty acid synthase alpha-subunit as reported previously (S. Saitoh, K. Takahashi, K. Nabeshima, Y. Yamashita, Y. Nakaseko, A. Hirata, M. Yanagida, J. Cell Biol. 134 (1996) 949--961). In this paper, lsd1 is considered to represent fas2. Here, three fas2 strains were investigated and found to have missense point mutations at different sites in the gene encoding the alpha-subunit of fatty acid synthase. The mutation affected only slightly the enzymatic activities monitored in vitro. Unexpectedly, abnormal phospholipids, phosphatidylcholine and phosphatidylethanolamine, both of which contain a very-long-chain fatty acyl residue (1-melissoyl-2-oleolyl-sn-glycero-3-phosphocholine and 1-melissoyl-2-oleolyl-sn-glycero-3-phosphoethanolamine), accumulated in fas2 strains in a temperature-sensitive manner. Rescue of the fas2 strains by addition of palmitate to the medium at restrictive temperature was accompanied by disappearance of these abnormal phospholipids. Accumulation of these lipids in membranes may cause alteration of various cellular functions.
裂殖酵母lsd1菌株表现出具有lsd表型的异常有丝分裂,即大小不等的子核以及非常厚的隔膜,其表型表达具有温度敏感性。如先前报道(S. Saitoh、K. Takahashi、K. Nabeshima、Y. Yamashita、Y. Nakaseko、A. Hirata、M. Yanagida,《细胞生物学杂志》134卷(1996年)949 - 961页),lsd1(+)基因是芽殖酵母FAS2基因的同源物,后者编码脂肪酸合酶α亚基。在本文中,lsd1被认为代表fas2。在此,对三个fas2菌株进行了研究,发现它们在脂肪酸合酶α亚基编码基因的不同位点存在错义点突变。该突变对体外监测的酶活性影响轻微。出乎意料的是,异常磷脂,即磷脂酰胆碱和磷脂酰乙醇胺,二者均含有非常长链的脂肪酰基残基(1 - 蜂花酰 - 2 - 油酰 - sn - 甘油 - 3 - 磷酸胆碱和1 - 蜂花酰 - 2 - 油酰 - sn - 甘油 - 3 - 磷酸乙醇胺),以温度敏感的方式在fas2菌株中积累。在限制温度下向培养基中添加棕榈酸可挽救fas2菌株,同时这些异常磷脂消失。这些脂质在膜中的积累可能导致各种细胞功能的改变。