1989
DOI: 10.1016/0167-4781(89)90037-7
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Cis- and trans-acting factors for transcription of the adenovirus 12 E1A gene

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Cited by 9 publications
(6 citation statements)
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“…The nucleotide sequences of all fragments were t Present address: Diagen, Hilden, Germany. determined in an Applied Biosystems 373A sequencer by using appropriate 19to 24-nucleotide-pair primers and the chain termination method (37). The nucleotide sequence of both DNA strands was determined over the entire molecule (see the primer locations in Fig.…”
Section: Methodsmentioning
confidence: 99%
“…The nucleotide sequences of all fragments were t Present address: Diagen, Hilden, Germany. determined in an Applied Biosystems 373A sequencer by using appropriate 19to 24-nucleotide-pair primers and the chain termination method (37). The nucleotide sequence of both DNA strands was determined over the entire molecule (see the primer locations in Fig.…”
Section: Methodsmentioning
confidence: 99%
“…Thus, for Ad12 it was shown by in vitro transcription assays that the promoters of both TS1 and TS2 are individually stimulated by cellular factors Nakanishi et al, 1987). Previous reports have indicated that the binding of nuclear factor-I (NF-I) to a region located near the left end of the Ad12 genome is involved in stimulation of TS1 (Koikeda et al, 1990 ;Shibata et al, 1989) and that the DNA-binding activity of NF-I might be inhibited by the E1A protein (Koikeda et al, 1990 ;Shibata-Sakurai et al, 1991). In addition, the E1A-stimulating factor 1 (ESF-1) was found to activate basal transcription from TS2 by interacting with a palindromic DNA sequence immediately upstream of the TATA box (Shibata-Sakurai et al, 1991, 1993.…”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, Ad12 possesses two functional transcriptional start sites located at nt 306 (TS1) and 445 (TS2). Both initiation sites are active at an early stage after infection with virus (Saito et al, 1981 ;Sawada & Fujinaga, 1980), resulting in a long and a short 13S-and 12S-primary transcript (Fujinaga et al, 1984 ;Nakanishi et al, 1987 ;Shibata et al, 1989).…”
Section: Introductionmentioning
confidence: 99%
“…Nuclear extracts were prepared from Ehrlich ascites tumor cells essentially by the procedure of Dignam et al (12). Cell-free transcription was done in a 25-,ul reaction mixture with 0.1 pmol of DNA templates and 10 ,ul of nuclear extracts, and transcripts were analyzed by primer extension as previously described (50,51). In primer extension, the CAT primer, 5'-CAACGGTGGTATATCCAGTG, was used for the Ad2 E3 gene, the human ,3-actin gene, and the proximal transcription of the Adl2 Ela gene, whereas the distal transcription of the Adl2 Ela gene was analyzed with the specific D primer (50).…”
Section: Methodsmentioning
confidence: 99%