Screening of human gene promoter activities using transfected-cell arrays.

Authors:
Xi Cheng, Anna Guerasimova, Thomas Manke, Philip Rosenstiel, Stefan Haas, Hans-Joerg Warnatz, Robert Querfurth, Wilfried Nietfeld, Dominique Vanhecke, Hans Lehrach, Marie-Laure Yaspo, Michal Janitz
Year of publication:
2010
Volume:
450
Issue:
1-2
Issn:
0378-1119
Journal title abbreviated:
GENE
Journal title long:
Gene : an international journal focusing on gene cloning and gene structure and function
Impact factor:
2.319
Abstract:
Promoters are the best characterized transcriptional regulatory sequences in complex genomes because of their predictable location immediately upstream of transcription start sites. Despite a substantial body of literature describing transcriptional promoters, the identification of true start sites for all human transcripts is far from complete. The same is true of the key structural and functional elements responsible for promoter action in different cell types. In order to identify elements responsible for promoter activity, we applied transfected-cell array technology to functionally evaluate promoters for genes involved in inflammatory bowel disease. Seventy-four promoters were examined by reverse transfection of a promoter-fluorescent reporter constructs into a human embryonic kidney cell line (HEK293T). Sixteen (21.6%) promoters were found to be active in HEK293 T cells. Correlations between promoter activity and endogenous transcript level were calculated, and 75% of active promoters were found to be associated with transcriptional activity of their gene counterparts. These results provide experimental evidence of promoter activity, which may aid in understanding the regulation of gene expression. Moreover, this is the first large-scale functional study of regulatory sequences to use a high-throughput transfected-cell array technique.