| Literature DB >> 16584612 |
Xue-Chun Lu1, Fang-Ding Lou, Wei-Dong Han, Xu-Dong Zhu, Yim-Ming Mu, Zhou-Min Xu, Li Yu.
Abstract
The study was aimed to analyze the characteristics of LRP16 gene promoter and its activity in order to explore the possible regulation mechanism of LRP16 gene expression. A 2.6 kb genomic DNA sequence of LRP16 5'-end was obtained from NCBI by BLAST software. The 7 target sequences between 0.2 - 2.6 kb from a healthy blood donor DNA sample were amplified by PCR, then identified by DNA sequencing and semi-nest PCR. The verified sequences were analyzed on-line. The results showed that the 7 target sequences were about 400 bp different from each other. All 7 sequences were the same to these GenBank described. At last, all 7 promoter sequences were ligated with luciferase vector, and then the luciferase activity was analyzed in HeLa cells. A known gene promoter sequence can be freely obtained from NCBI database. It is concluded that LRP16 promoter is a standard type II promoter and its activity is strongest in the region from -200 to -600 bp.Entities:
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Year: 2006 PMID: 16584612
Source DB: PubMed Journal: Zhongguo Shi Yan Xue Ye Xue Za Zhi ISSN: 1009-2137