The E4 promoter of adenovirus type 2 contains an E1A dependent cis-actlng element (original) (raw)
Journal Article
Institut de Recherches Scientiliques sur Ic Cancer, Centre National de la Recherche Scientifique
94800 Villejuif, France
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Institut de Recherches Scientiliques sur Ic Cancer, Centre National de la Recherche Scientifique
94800 Villejuif, France
Search for other works by this author on:
Received:
09 October 1986
Accepted:
28 October 1986
Published:
11 November 1986
Cite
Pascale Gilardi, Michel Perricaudet, The E4 promoter of adenovirus type 2 contains an E1A dependent cis-actlng element, Nucleic Acids Research, Volume 14, Issue 22, 11 November 1986, Pages 9035–9049, https://doi.org/10.1093/nar/14.22.9035
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Abstract
To study how the E1A polypeptides of adenovirus type 2 regulate transcription, we have constructed chimeric plasnids containing the bacterial gene encoding chloranphenicol acetyl transferase (CAT) under the control of either the wild type or the deleted E4 promoter of adenovirus type 2. Our previous results showed that promoter sequences located upstream from position −158, as measured from the cap site, are essential to the transactivation process. From a new set of deletion mutants, we now show that two regions, located between positions −239 and −218 and between positions −179 and −158, are involved in the E1A transactivation process. The deletion of only one of them does not significantly alter the E1A Induction process compared with the wild type. Moreover, we show that these two regions lie within a DNA fragment which possesses the properties of an E1A—inducible “enhancer—like” element. In addition, the DNA fragment which contains this enhancer element is also able to confer the E1A inducibility to a heterologous promoter.
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