Mohamed A H, Chirala S S, Mody N H, Huang W Y, Wakil S J
Verna and Marrs McLean Department of Biochemistry, Baylor College of Medicine, Houston, Texas 77030.
J Biol Chem. 1988 Sep 5;263(25):12315-25.
The yeast fatty acid synthase consists of two multifunctional proteins, alpha and beta, arranged in an alpha 6 beta 6 complex with a molecular weight of 2.4 x 10(6). Five of the seven enzymatic activities reside in the beta subunit, while the remaining two activities, beta-ketoacyl synthase and beta-ketoacyl reductase, and the domain of the acyl carrier protein, with its prosthetic group, 4'-phosphopantetheine, are in the alpha subunit. The genes FAS1 and FAS2 coding for beta and alpha subunits, respectively, have been cloned and the sequence of FAS1 has been reported (Chirala, S. S., Kuziora, M. A., Spector, D. M., and Wakil, S. J. (1987) J. Biol. Chem. 262, 4231-4240). In this study, we present the nucleotide sequence of the FAS2 gene. The sequence has an open reading frame, coding for a protein of 1894 amino acids with a calculated molecular weight of 207,863. The location of the serine site of attachment of the prosthetic group of the acyl carrier protein domain and the active cysteine-SH site of beta-ketoacyl synthase have been identified at residues 180 and 1312, respectively, in the deduced amino acid sequence. A putative NADPH binding site of beta-ketoacyl reductase has been suggested at residue 1038 based on the similarities to the consensus amino acid sequences -Gly-Ser-Ala- of the pyridine nucleotide enzymes. We could not find any sequence homology in the 5' flanking sequence of the FAS1 and FAS2 genes that would suggest common regulatory function. However, in the sequence of these two genes there is an identical eight-base pair sequence TCATTATG at the translational initiation site suggesting that the subunit stoichiometry probably results from equal translational efficiency of the mRNAs of both FAS1 and FAS2 genes. The S1 endonuclease mapping suggests that there is a transcriptional initiation site at about 40 nucleotides upstream of the first ATG codon and a transcriptional termination site about 300 nucleotides downstream of the TAG stop codon. The gene does not contain introns as no intron consensus TACTAAC have been found in the sequence.
酵母脂肪酸合酶由两种多功能蛋白α和β组成,它们以α6β6复合物的形式排列,分子量为2.4×10⁶。七种酶活性中的五种存在于β亚基中,而其余两种活性,即β-酮脂酰合酶和β-酮脂酰还原酶,以及酰基载体蛋白结构域及其辅基4'-磷酸泛酰巯基乙胺,则存在于α亚基中。分别编码β和α亚基的基因FAS1和FAS2已被克隆,并且FAS1的序列已被报道(Chirala, S. S., Kuziora, M. A., Spector, D. M., and Wakil, S. J. (1987) J. Biol. Chem. 262, 4231 - 4240)。在本研究中,我们展示了FAS2基因的核苷酸序列。该序列有一个开放阅读框,编码一个1894个氨基酸的蛋白质,计算分子量为207,863。在推导的氨基酸序列中,分别在第180位和第1312位残基处鉴定出了酰基载体蛋白结构域辅基的丝氨酸连接位点和β-酮脂酰合酶的活性半胱氨酸-SH位点。基于与吡啶核苷酸酶的共有氨基酸序列-Gly-Ser-Ala-的相似性,在第1038位残基处推测了β-酮脂酰还原酶的一个假定的NADPH结合位点。我们在FAS1和FAS2基因的5'侧翼序列中未发现任何表明共同调节功能的序列同源性。然而,在这两个基因的序列中,翻译起始位点有一个相同的八碱基对序列TCATTATG,这表明亚基化学计量可能源于FAS1和FAS2基因mRNA的相等翻译效率。S1核酸酶图谱分析表明,在第一个ATG密码子上游约40个核苷酸处有一个转录起始位点,在TAG终止密码子下游约300个核苷酸处有一个转录终止位点。该基因不包含内含子,因为在序列中未发现内含子共有序列TACTAAC。