Yang Y, Martin L, Cuzin F, Mattei M G, Rassoulzadegan M
INSERM U. 273, Université de Nice, Nice, 06108, France.
Genomics. 1996 Jul 1;35(1):24-9. doi: 10.1006/geno.1996.0318.
The genomic structure of the mouse gene encoding the CDEBP protein has been established. The protein was initially identified on the basis of its ability to bind the CDEI motif (GTCACATG). The same locus has been independently described under the name APLP2, on the basis of sequence similarities with the Amyloid Precursor Protein (APP). The exon-intron distribution of Cdebp appears strikingly similar to that of the App gene in the regions encoding the conserved domains, with a divergent structure in the other parts. The transcription start site has been localized, and sequences with promoter activity have been identified immediately upstream of it by their ability to direct the expression of a reporter luciferase gene in transfected cells. This region is devoid of either TATA or CAAT boxes. The gene has been mapped to mouse chromosome 9 by in situ hybridization on metaphase chromosomes.
编码CDEBP蛋白的小鼠基因的基因组结构已被确定。该蛋白最初是根据其结合CDEI基序(GTCACATG)的能力而被鉴定出来的。基于与淀粉样前体蛋白(APP)的序列相似性,同一基因座已被独立地描述为APLP2。在编码保守结构域的区域,Cdebp的外显子-内含子分布与App基因的分布惊人地相似,而在其他部分则具有不同的结构。转录起始位点已被定位,并且通过它们在转染细胞中指导报告荧光素酶基因表达的能力,在其上游紧邻处鉴定出了具有启动子活性的序列。该区域没有TATA盒或CAAT盒。通过中期染色体原位杂交,该基因已被定位到小鼠9号染色体上。