Principaud E, Spohr G
Université de Genève, Département de Biologie Cellulaire, Switzerland.
Nucleic Acids Res. 1991 Jun 11;19(11):3081-8. doi: 10.1093/nar/19.11.3081.
The structure of the two Xenopus laevis c-myc I and c-myc II genes has been investigated by isolating and sequencing genomic and cDNAs clones. In oocytes, c-myc I mRNAs represent 80-90% of the overall amount of c-myc transcripts. The c-myc I expression is controlled primarily by two differentially regulated tandem promoters P1 and P2 which are separated by 50 bases. During oogenesis, maternal c-myc I mRNAs, are transcribed from both promoters whereas zygotic transcripts seem to initiate only from the P2 promoter. Sequence comparison between the promoter regions of c-myc I and II genes reveals the insertion in the c-myc I promoter region, between positions -831 and -389 relative to the P1 start site of a repetitive element. Comparison of X.laevis and mammalian c-myc promoter sequences reveals furthermore the conservation of cis-regulatory elements, including a motif known to be a negative regulator of the human c-myc transcription, a purine rich region, a binding site for the E2-F transcription factor and three SP1 binding sites. Finally, we report characterization of a new c-myc I mRNA which differ at the 5' end. Transcripts are possibly initiated at a putative alternative promoter located further upstream in the genome, and undergoes alternative splicing.
通过分离和测序基因组及cDNA克隆,对非洲爪蟾的两个c-myc I和c-myc II基因的结构进行了研究。在卵母细胞中,c-myc I mRNA占c-myc转录本总量的80%-90%。c-myc I的表达主要受两个调控方式不同的串联启动子P1和P2控制,它们相隔50个碱基。在卵子发生过程中,母源c-myc I mRNA由两个启动子转录,而合子转录本似乎仅从P2启动子起始。c-myc I和II基因启动子区域的序列比较显示,在c-myc I启动子区域相对于P1起始位点的-831至-389位之间插入了一个重复元件。此外,非洲爪蟾与哺乳动物c-myc启动子序列的比较揭示了顺式调控元件的保守性,包括一个已知为人类c-myc转录负调控因子的基序、一个富含嘌呤的区域、一个E2-F转录因子结合位点和三个SP1结合位点。最后,我们报道了一种在5'端存在差异的新c-myc I mRNA的特征。转录本可能起始于基因组中更上游的一个假定的替代启动子,并经历可变剪接。