Yokoyama Kazuaki, Nakagawa Miyuki, Satoh Masayuki, Saitoh Shigeaki, Dohmae Naoshi, Harada Ayako, Satoh Noriko, Karasawa Ken, Takio Koji, Yanagida Mitsuhiro, Inoue Keizo
Faculty of Pharmaceutical Sciences, Teikyo University, Suarashi, Sagamiko-machi, Sagamihara-shi, Kanagawa, Japan.
J Biochem. 2008 Mar;143(3):369-75. doi: 10.1093/jb/mvm232. Epub 2007 Dec 13.
The fission yeast lsd1/fas2 strain carries a temperature-sensitive mutation of the fatty-acid-synthase alpha-subunit, exhibiting an aberrant mitosis lsd phenotype, with accumulation of very-long-chain fatty-acid-containing phospholipid (VLCFA-PL). A novel 90-kDa protein, Lsd90 (SPBC16E9.16c), was found to be newly expressed in small particle-like structures in lsd1/fas2 cells under restrictive conditions. Two mismatches leading to a double frame shift were found between the sequences of the lsd90(+) gene registered in the genomic database and the sequences determined experimentally at the amino acid, cDNA and genomic DNA levels. Unexpectedly, overexpression and disruption of the lsd90(+) gene in either lsd1/fas2 or wild-type cells did not affect either cell growth or expression of the lsd phenotype. The amounts of VLCFA-PL that accumulated in lsd90-overexpressing lsd1/fas2 cells were significantly lower than those in lsd1/fas2 cells, suggesting the involvement of Lsd90 in the metabolism of VLCFA-PL.
裂殖酵母lsd1/fas2菌株携带脂肪酸合酶α亚基的温度敏感突变,表现出异常的有丝分裂lsd表型,伴有含超长链脂肪酸的磷脂(VLCFA-PL)积累。发现一种新的90 kDa蛋白Lsd90(SPBC16E9.16c)在限制条件下于lsd1/fas2细胞的小颗粒样结构中新生表达。在基因组数据库中登记的lsd90(+)基因序列与在氨基酸、cDNA和基因组DNA水平上通过实验确定的序列之间发现了两个导致双移码的错配。出乎意料的是,在lsd1/fas2或野生型细胞中过表达和破坏lsd90(+)基因均不影响细胞生长或lsd表型的表达。在过表达lsd90的lsd1/fas2细胞中积累的VLCFA-PL量显著低于lsd1/fas2细胞中的量,这表明Lsd90参与VLCFA-PL的代谢。