Swendeman S L, Spielholz C, Jenkins N A, Gilbert D J, Copeland N G, Sheffery M
Molecular Biology Program, Cornell University, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.
J Biol Chem. 1994 Apr 15;269(15):11663-71.
We recently cloned murine and human cDNAs that encode CP2, a cellular transcription factor that interacts with the alpha-globin promoter as well as with additional cellular and viral promoter elements. We have now characterized the genomic structure, chromosome location, promoter, and expression pattern of the factor. Genes for the murine and human mRNAs contained 16 and 15 exons, respectively. Both genes spanned approximately 30 kilobases of chromosomal DNA, and among coding exons, all exon/intron boundaries were conserved. The human gene for CP2 was found to reside on chromosome 12 while the murine gene mapped to the distal end of chromosome 15, near Gdc-1, Wnt-1, and Rarg, a region syntenic with human chromosome 12. The murine and human promoters initiated mRNAs at multiple start sites in a conserved region that spanned more than 450 nucleotides. Lastly, a study of the pattern of CP2 gene expression showed that the factor was expressed in all adult and fetal murine tissues examined from at least day 9.5 of development.
我们最近克隆了编码CP2的小鼠和人类cDNA,CP2是一种细胞转录因子,它与α-珠蛋白启动子以及其他细胞和病毒启动子元件相互作用。我们现在已经对该因子的基因组结构、染色体定位、启动子和表达模式进行了表征。小鼠和人类mRNA的基因分别包含16个和15个外显子。两个基因都跨越了大约30千碱基的染色体DNA,并且在编码外显子中,所有外显子/内含子边界都是保守的。发现人类CP2基因位于12号染色体上,而小鼠基因定位于15号染色体的远端,靠近Gdc-1、Wnt-1和Rarg,该区域与人类12号染色体同线。小鼠和人类启动子在跨越超过450个核苷酸的保守区域中的多个起始位点起始mRNA。最后,对CP2基因表达模式的研究表明,该因子在至少从发育第9.5天开始检查的所有成年和胎儿小鼠组织中均有表达。