Klenova E M, Fagerlie S, Filippova G N, Kretzner L, Goodwin G H, Loring G, Neiman P E, Lobanenkov V V
Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom.
J Biol Chem. 1998 Oct 9;273(41):26571-9. doi: 10.1074/jbc.273.41.26571.
CTCF is a multifunctional transcription factor encoded by a novel candidate tumor suppressor gene (Filippova, G. N., Lindblom, A., Meinke, L. J., Klenova, E. M., Neiman, P. E., Collins, S. J., Doggett, N. D., and Lobanenkov, V. V. (1998) Genes Chromosomes Cancer 22, 26-36). We characterized genomic organization of the chicken CTCF (chCTCF) gene, and studied the chCTCF promoter. Genomic locus of chCTCF contains a GC-rich untranslated exon separated from seven coding exons by a long intron. The 2-kilobase pair region upstream of the major transcription start site contains a CpG island marked by a "Not-knot" that includes sequence motifs characteristic of a TATA-less promoter of housekeeping genes. When fused upstream of a reporter chloramphenicol acetyltransferase gene, it acts as a strong transcriptional promoter in transient transfection experiments. The minimal 180-base pair chCTCF promoter region that is fully sufficient to confer high level transcriptional activity to the reporter contains high affinity binding element for the transcription factor YY1. This element is strictly conserved in chicken, mouse, and human CTCF genes. Mutations in the core nucleotides of the YY1 element reduce transcriptional activity of the minimal chCTCF promoter, indicating that the conserved YY1-binding sequence is critical for transcriptional regulation of vertebrate CTCF genes. We also noted in the chCTCF promoter several elements previously characterized in cell cycle-regulated genes, including the "cell cycle-dependent element" and "cell cycle gene homology region" motifs shown to be important for S/G2-specific up-regulation of cdc25C, cdc2, cyclin A, and Plk (polo-like kinase) gene promoters. Presence of the cell cycle-dependent element/cell cycle gene homology region element suggested that chCTCF expression may be cell cycle-regulated. We show that both levels of the endogenous chCTCF mRNA, and the activity of the stably transfected chCTCF promoter constructs, increase in S/G2 cells.
CTCF是一种多功能转录因子,由一个新的候选肿瘤抑制基因编码(菲利波娃,G.N.,林德布洛姆,A.,梅因克,L.J.,克莱诺娃,E.M.,内曼,P.E.,柯林斯,S.J.,多格特,N.D.,和洛巴年科夫,V.V.(1998年)《基因、染色体与癌症》22卷,26 - 36页)。我们对鸡CTCF(chCTCF)基因的基因组结构进行了表征,并研究了chCTCF启动子。chCTCF的基因组位点包含一个富含GC的非编码外显子,与七个编码外显子被一个长内含子隔开。主要转录起始位点上游的2千碱基对区域包含一个以“Not - knot”标记的CpG岛,其中包括管家基因无TATA启动子的特征性序列基序。当与报告氯霉素乙酰转移酶基因上游融合时,它在瞬时转染实验中作为一个强转录启动子起作用。完全足以赋予报告基因高水平转录活性的最小180碱基对chCTCF启动子区域包含转录因子YY1的高亲和力结合元件。该元件在鸡、小鼠和人类CTCF基因中严格保守。YY1元件核心核苷酸的突变降低了最小chCTCF启动子的转录活性,表明保守的YY1结合序列对脊椎动物CTCF基因的转录调控至关重要。我们还在chCTCF启动子中注意到了一些先前在细胞周期调控基因中表征的元件,包括“细胞周期依赖性元件”和“细胞周期基因同源区域”基序,这些基序已被证明对cdc25C、cdc2、细胞周期蛋白A和Plk(类polo激酶)基因启动子的S/G2特异性上调很重要。细胞周期依赖性元件/细胞周期基因同源区域元件的存在表明chCTCF表达可能受细胞周期调控。我们表明,内源性chCTCF mRNA水平以及稳定转染的chCTCF启动子构建体的活性在S/G2期细胞中均增加。