Kaestner K H, Ntambi J M, Kelly T J, Lane M D
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
J Biol Chem. 1989 Sep 5;264(25):14755-61.
Previously we isolated and characterized a differentially expressed gene from mouse 3T3-L1 preadipocytes that encodes stearoyl-CoA desaturase (SCD1; Ntambi, J. M., Buhrow, S. A., Kaestner, K. H., Christy, R. J., Sibley, E., Kelly, T. J., Jr., and Lane, M. D. (1988) J. Biol. Chem. 263, 17291-17300). Genomic Southern blot analysis indicated the existence of another closely related gene. Here we report the isolation and characterization of this gene and the corresponding cDNA which encode a second stearoyl-CoA desaturase, SCD2, 3T3-L1 adipocytes. SCD2 cDNA is 5 kilobase pairs in length and encodes a protein of 358 amino acids with greater than 87% amino acid sequence identity to SCD1. RNase protection analysis reveals a 10-fold increase in the expression of SCD2 mRNA during 3T3-L1 preadipocyte differentiation. SCD2 mRNA is expressed constitutively at a high level in brain, is not expressed in liver, and its expression in kidney, adipose, and lung tissue is increased greatly by shifting mice from a diet containing unsaturated fatty acids to a diet devoid of fat. The tissue distribution and the dietary alteration of SCD1 mRNA expression differs markedly from that of SCD2 mRNA being absent from brain, constitutive in adipose tissue, and subject to negative control in liver by feeding a diet containing unsaturated fatty acids. The SCD2 gene spans approximately 15 kilobase pairs and consists of six exons and five introns, with intron/exon junctions similar to those of SCD1. As determined by primer extension analysis the start site of transcription maps 300 nucleotides upstream of the initiator methionine codon. Unlike the SCD1 gene, SCD2 lacks a typical "TATA" box in the 5'-flanking region, but has two "CCAAT" boxes at positions -90 and -135 relative to the transcription initiation site. The SCD2 promoter contains a 140-base pair sequence (located between nucleotides -54 and -201) which possesses 77% sequence identity to a region (located between nucleotides -472 and -325) in the SCD1 promoter. There is a GC-rich sequence in the SCD2 promoter (at nucleotide -175) similar to the binding site for the nuclear transcription factor Sp1 as well as an element with homology to the core consensus sequence for the glucocorticoid regulatory element position -500 and a potential CCAAT box/enhance binding protein sequence at position -540. The SCD gene family provides a new model system for the study of differentiation-induced as well as tissue-specific metabolite controlled gene expression.
此前,我们从小鼠3T3-L1前脂肪细胞中分离并鉴定了一个差异表达基因,该基因编码硬脂酰辅酶A去饱和酶(SCD1;恩坦比,J.M.,布罗,S.A.,凯斯特纳,K.H.,克里斯蒂,R.J.,西布利,E.,凯利,T.J.,Jr.,和莱恩,M.D.(1988年)《生物化学杂志》263,17291 - 17300)。基因组Southern印迹分析表明存在另一个密切相关的基因。在此,我们报告该基因以及相应cDNA的分离和鉴定,它们编码第二种硬脂酰辅酶A去饱和酶SCD2,存在于3T3-L1脂肪细胞中。SCD2 cDNA长度为5千碱基对,编码一个由358个氨基酸组成的蛋白质,与SCD1的氨基酸序列同一性大于87%。核糖核酸酶保护分析显示,在3T3-L1前脂肪细胞分化过程中,SCD2 mRNA的表达增加了10倍。SCD2 mRNA在脑中持续高水平表达,在肝脏中不表达,并且通过将小鼠从含不饱和脂肪酸的饮食改为无脂肪饮食,其在肾脏、脂肪和肺组织中的表达大幅增加。SCD1 mRNA表达的组织分布和饮食改变与SCD2 mRNA明显不同,SCD1 mRNA在脑中不存在,在脂肪组织中持续存在,并且通过喂食含不饱和脂肪酸的饮食在肝脏中受到负调控。SCD2基因跨度约15千碱基对,由6个外显子和5个内含子组成,内含子/外显子连接与SCD1相似。通过引物延伸分析确定,转录起始位点位于起始甲硫氨酸密码子上游300个核苷酸处。与SCD1基因不同,SCD2在5'侧翼区域缺乏典型的“TATA”框,但在相对于转录起始位点的 - 90和 - 135位置有两个“CCAAT”框。SCD2启动子包含一个140碱基对的序列(位于核苷酸 - 54和 - 201之间),与SCD1启动子中的一个区域(位于核苷酸 - 472和 - 325之间)具有77%的序列同一性。SCD2启动子中有一个富含GC的序列(在核苷酸 - 175处),类似于核转录因子Sp1的结合位点,以及一个与糖皮质激素调节元件核心共有序列在 - 500位置同源的元件和一个在 - 540位置的潜在CCAAT框/增强子结合蛋白序列。SCD基因家族为研究分化诱导以及组织特异性代谢物控制的基因表达提供了一个新的模型系统。