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大鼠AJ18基因5'侧翼区的特征分析

Characterization of the 5'-flanking region of the rat AJ18 gene.

作者信息

Jheon Andrew H, Suzuki Naoto, Nishiyama Takehisa, Cheifetz Sela, Sodek Jaro, Ganss Bernhard

机构信息

Department of Biochemistry, University of Toronto, Room 239 Fitzgerald Building, 150 College Street, Toronto, Ont. M5S 3E2, Canada.

出版信息

Gene. 2003 May 22;310:203-13. doi: 10.1016/s0378-1119(03)00553-5.

DOI:10.1016/s0378-1119(03)00553-5
PMID:12801648
Abstract

Krüppel-associated box (KRAB) domains are present in one-third of all C(2)H(2) zinc finger containing proteins, making the KRAB/C(2)H(2) proteins one of the largest known families of putative transcription repressors. AJ18 has been identified as a novel KRAB/C(2)H(2) gene that is involved in the differentiation of osteogenic cells. To study the regulation of expression of the AJ18 gene, the 5'-flanking region of the AJ18 gene was obtained by screening a rat genomic library. This region was sequenced, and the transcription start site mapped by primer extension. The AJ18 gene consists of at least four exons, the first exon coding for an unusually long 2.3 kb 5'-UTR region. A putative internal ribosome entry site, immediately upstream of the translation initiation site, is indicated from the complementarity of a 12 nucleotide sequence with a region in the rat 18S rRNA. Chimeric constructs encompassing the region surrounding the transcription start site (-77-+171), as well as constructs with additional 1.9 kb upstream from this region revealed strong transcriptional activity when ligated to a luciferase reporter gene and tested in transient transfection assays. This activity was lost on deletion of the 5'-flanking region to -77. In addition, transcriptional activity was progressively lost with the inclusion of downstream sequences extending into the 5'-UTR. Several known response elements for proteins such as Runx2, NFkappaB, Smads, Sp1, and Ets1 are retained within the conserved sequences of rat and mouse AJ18, which was retrieved from mouse genomic libraries. Interestingly, the transcriptional activity was approximately 100-fold higher in the osteocarcinoma cell line ROS 2.8/17 compared to the fibroblast-like C3H10T1/2. Notably, this is the first gene promoter from the large KRAB/C(2)H(2) zinc finger family of proteins to be identified and characterized.

摘要

克勒ppel相关盒(KRAB)结构域存在于所有含C(2)H(2)锌指蛋白的三分之一中,使得KRAB/C(2)H(2)蛋白成为已知最大的假定转录抑制因子家族之一。AJ18已被鉴定为一种参与成骨细胞分化的新型KRAB/C(2)H(2)基因。为了研究AJ18基因的表达调控,通过筛选大鼠基因组文库获得了AJ18基因的5'侧翼区域。对该区域进行了测序,并通过引物延伸确定了转录起始位点。AJ18基因至少由四个外显子组成,第一个外显子编码一个异常长的2.3 kb 5'-UTR区域。从一个12核苷酸序列与大鼠18S rRNA中的一个区域的互补性表明,在翻译起始位点上游紧邻处存在一个假定的内部核糖体进入位点。包含转录起始位点周围区域(-77-+171)的嵌合构建体,以及该区域上游额外1.9 kb的构建体,当与荧光素酶报告基因连接并在瞬时转染实验中测试时,显示出强大的转录活性。当5'侧翼区域缺失至-77时,这种活性丧失。此外,随着包含延伸到5'-UTR的下游序列,转录活性逐渐丧失。在从小鼠基因组文库中检索到的大鼠和小鼠AJ18的保守序列中保留了几种已知的蛋白质反应元件,如Runx2、NFkappaB、Smads、Sp1和Ets1。有趣的是,与成纤维细胞样的C3H10T1/2相比,骨肉瘤细胞系ROS 2.8/17中的转录活性大约高100倍。值得注意的是,这是第一个从大型KRAB/C(2)H(2)锌指蛋白家族中鉴定和表征的基因启动子。

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