Romero E E, Deo R, Velazquez-Estades L J, Roth D A
Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Biochem Biophys Res Commun. 1998 Jul 30;248(3):783-8. doi: 10.1006/bbrc.1998.8987.
The vitamin K-dependent gamma-glutamyl carboxylase gene was cloned from a rat liver genomic DNA library and the structural organization of this gene was determined. The carboxylase gene is 16.3 kb in length and contains 15 exons and 14 introns. DNA sequence analysis revealed that all 14 introns were U2-Type GT-AG introns. A 2.8-kb DNA fragment corresponding to the 5'-flanking region of the cloned gene demonstrated transcriptional activity in a rat liver cell line that is known to express the endogenous carboxylase gene. DNA sequence analysis of the proximal 331 bp of this 5'-flanking sequence reveals the absence of an identifiable TATA box. Consensus sequences for several transcription factors that may be important in regulating its tissue specific expression were identified. The isolation and characterization of the rat carboxylase gene provides essential information for the analysis of its regulation in vitro and in transgenic animal models.
从大鼠肝脏基因组DNA文库中克隆出维生素K依赖性γ-谷氨酰羧化酶基因,并确定了该基因的结构组织。羧化酶基因长度为16.3kb,包含15个外显子和14个内含子。DNA序列分析表明,所有14个内含子均为U2型GT-AG内含子。与克隆基因5'侧翼区域相对应的一个2.8kb DNA片段在已知表达内源性羧化酶基因的大鼠肝细胞系中表现出转录活性。对该5'侧翼序列近端331bp进行DNA序列分析,发现没有可识别的TATA框。确定了几个可能对调节其组织特异性表达很重要的转录因子的共有序列。大鼠羧化酶基因的分离和鉴定为体外分析其调控以及转基因动物模型提供了重要信息。