小鼠忍尿蛋白基因组DNA序列及转录因子结合位点

Ae Ran Moon, G. Oh, Jae Wha Kim, Y. Cho, I. Choe
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引用次数: 4

摘要

通过筛选细菌人工染色体(BAC)小鼠129/SvJ基因组DNA文库,克隆并测序了小鼠忍尿素基因的全基因组DNA序列。小鼠ninjurin基因包括4个外显子,可翻译序列包含在前3个外显子中。小鼠ninjurin基因的推定启动子区域缺乏共识的“CAAT”或“TATA”序列。然而,利用含有小鼠忍者蛋白和报告基因启动子序列的构建体,在瞬时转染实验中证明了启动子的活性。该启动子区域的核苷酸序列与已有报道的人类忍者基因的DNA序列同源性为83%,显示了两者之间的高度保守性。DNA序列分析确定了小鼠忍者蛋白的启动子和多种转录因子的结合位点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genomic DNA Sequence and Transcription Factor Binding Sites of Mouse Ninjurin
The complete genomic DNA sequence of mouse ninjurin gene has been cloned and sequenced by screening a bacterial artificial chromosome (BAC) library of mouse 129/SvJ genomic DNA. The mouse ninjurin gene comprises four exons and the translatable sequences are included in the first three exons. The putative promoter region of the mouse ninjurin gene lacks the consensus “CAAT” or “TATA” sequence. Nonetheless, it has demonstrated the promoter activity in transient transfection experiment using the construct containing putative promoter sequence of mouse ninjurin and reporter gene. The nucleotide sequence of the putative promoter region shows 83% homology with the corresponding DNA sequence of human ninjurin gene that had been previously reported, and reveals a high degree of conservation between the two species. Analysis of the DNA sequence identified the putative promoters and the binding sites for a variety of transcription factors of mouse ninjurin.
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