Remmers E F, Yang J Q, Marcu K B
EMBO J. 1986 May;5(5):899-904. doi: 10.1002/j.1460-2075.1986.tb04301.x.
We have investigated the nature of regulatory sequences within the vicinity of the murine c-myc locus by analyzing the expression of myc-chloramphenicol acetyl transferase (CAT) vectors transfected into a human lymphoblastoid cell line (BJAB) and a monkey fibroblast line (COS). CAT enzymatic assays and S1 nuclease protection experiments reveal that a negative element resides 428-1188 bp 5' of the first c-myc promoter, P1. This 760-bp segment of 5'-flanking c-myc DNA dramatically inhibits CAT gene expression in the pSV2CAT vector when placed in either orientation approximately 1.7 kb 3' (and approximately 3.2 kb 5' on the circular plasmid) from the SV40 promoter region. By employing this strategy, we were unable to identify an analogous DNA segment that is closer to or within the first c-myc exon. We propose that this 5' c-myc region be termed a 'dehancer' since this negative element has the opposite properties of a transcriptional enhancer.
我们通过分析转染入人淋巴母细胞系(BJAB)和猴成纤维细胞系(COS)的myc-氯霉素乙酰转移酶(CAT)载体的表达,研究了小鼠c-myc基因座附近调控序列的性质。CAT酶活性测定和S1核酸酶保护实验表明,在第一个c-myc启动子P1的5'端428 - 1188 bp处存在一个负调控元件。当c-myc基因5'侧翼DNA的这个760 bp片段以任何方向置于距SV40启动子区域约1.7 kb下游(在环状质粒上约3.2 kb上游)时,它会显著抑制pSV2CAT载体中CAT基因的表达。通过采用这种策略,我们未能鉴定出更靠近第一个c-myc外显子或位于其内部的类似DNA片段。我们建议将这个c-myc基因5'区域称为“去增强子”,因为这个负调控元件具有与转录增强子相反的特性。