Dvorák M, Urbánek P, Bartůnĕk P, Paces V, Vlach J, Pecenka V, Arnold L, Trávnicek M, Ríman J
Institute of Molecular Genetics, Czechoslovak Academy of Sciences, Prague.
Nucleic Acids Res. 1989 Jul 25;17(14):5651-64. doi: 10.1093/nar/17.14.5651.
The nucleotide sequence of an 8.2-kb DNA fragment from the 5' proximal part of the chicken myb proto-oncogene spanning 1761 nucleotides upstream and 6436 nucleotides downstream from a presumed c-myb initiation codon was determined. A 3.3-kb G + C-rich region found in this sequence had also other features characterizing CpG islands, i.e. no CpG underrepresentation and lack of CpG methylation. In haematopoietic tissues c-myb mRNA synthesis starts in two major regions of the CpG island, namely 98 to 108 and 143 to 145 nucleotides upstream from the c-myb initiation codon. These two regions are in or close to the 124-bp evolutionarily conserved element located in the middle part of the CpG island. No alternative splicing of the 5' end of c-myb mRNA suggested earlier (1,2) was observed. The c-myb promoter contains neither TATA nor CAAT box-like structures at the usual positions. Instead, numerous potential Sp1 factor binding sites were found both upstream and downstream from the transcription initiation sites. Moreover, consensus v-myb protein DNA-binding sites were revealed in the promoter region and in sequences downstream from it.
测定了鸡原癌基因myb 5'近端一个8.2 kb DNA片段的核苷酸序列,该片段跨越推测的c-myb起始密码子上游1761个核苷酸和下游6436个核苷酸。在该序列中发现的一个3.3 kb富含G + C的区域还具有其他表征CpG岛的特征,即不存在CpG低丰度现象且缺乏CpG甲基化。在造血组织中,c-myb mRNA合成起始于CpG岛的两个主要区域,即c-myb起始密码子上游98至108个核苷酸以及143至145个核苷酸处。这两个区域位于CpG岛中部的124 bp进化保守元件内或附近。未观察到先前报道的(1,2)c-myb mRNA 5'端的可变剪接。c-myb启动子在通常位置既不包含TATA盒也不包含CAAT盒样结构。相反,在转录起始位点的上游和下游均发现了许多潜在的Sp1因子结合位点。此外,在启动子区域及其下游序列中发现了共有v-myb蛋白DNA结合位点。