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Binding sites of HeLa cell nuclear proteins on the upstream region of adenovirus type 5 E1A gene
Author(s) -
Koichi Yoshida,
Mitsuo Narita,
Kei Fujinaga
Publication year - 1989
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/17.23.10015
Subject(s) - caat box , biology , tata box , microbiology and biotechnology , binding site , enhancer , hypersensitive site , deoxyribonuclease i , promoter , dna binding site , consensus sequence , regulatory sequence , transcription factor , histone octamer , dna , dna binding protein , gene , gene expression , genetics , peptide sequence , nucleosome , chromatin , base sequence
Twenty one binding sites of HeLa cell nuclear proteins were identified on the upstream region of adenovirus type 5 E1A gene using DNase I footprint assay. The proximal promoter region contained five binding sites that overlapped the cap site, TATA box, TATA-like sequence, CCAAT box, and -100 region relative to the E1A cap site(+1). The -190 region was a potential site for octamer-motif binding proteins, such as NFIII and OBP100. An upstream copy of the E1A enhancer element 1 was the site for a factor (E1A-F) with the binding specificity of XGGAYGT (X = A, C; Y = A, T). E1A-F factor also bound to three other sites, one of which coincided with the distal E1A enhancer element. The distal element also contained a potential site for ATF factor. The adenovirus minimal origin of DNA replication competed for DNA-protein complex formation on the CCAAT and TATA box region and the -190 region, suggesting that these regions interacted with a common or related factor.

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