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Open AccessJournal ArticleDOI

A cellular protein, activating transcription factor, activates transcription of multiple E1A-inducible adenovirus early promoters

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TLDR
It is demonstrated here that E4F1 and E2A-EF have identical DNA-binding specificity, which indicates a significant role for ATF in E1A-mediated transcriptional activation.
Abstract: 
We have examined the relationship between sequence-specific DNA-binding proteins that activate transcription of E1A-inducible adenovirus early promoters. Factors previously referred to as E4F1 and E2A-EF bind to the E4 and E2A promoters, respectively. We demonstrate here that E4F1 and E2A-EF have identical DNA-binding specificity. Moreover, E4F1 and E2A-EF both activate transcription of the E4 and E2A promoters in vitro. These findings demonstrate that E4F1 and E2A-EF are the same factor, which we have designated activating transcription factor, or ATF. In addition to the E4 and E2A promoters, ATF binds to an important functional element of the E1A-inducible E3 promoter. Interaction of a common activator protein, ATF, with multiple E1A-inducible early viral promoters, suggests a significant role for ATF in E1A-mediated transcriptional activation.

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CREB: a stimulus-induced transcription factor activated by a diverse array of extracellular signals.

TL;DR: The molecular mechanisms by which Ser133-phosphorylated CREB activates transcription, intracellular signaling pathways that lead to phosphorylation ofCREB at Ser133, and features of each signaling pathway that impart specificity at the level of CREB activation are discussed.
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How eukaryotic transcriptional activators work

Mark Ptashne
- 20 Oct 1988 - 
TL;DR: A specific protein, bound to DNA, can activate transcription of a wide array of genes in many eukaryotes and is controlled by the immune system.
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Cross-family dimerization of transcription factors Fos/Jun and ATF/CREB alters DNA binding specificity.

TL;DR: It is suggested that the Fos/Jun and ATF/CREB families of transcription factors, which function in coupling extracellular signals to alterations in expression of specific target genes, can be grouped into a superfamily of transcription factor.
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Phosphorylation-induced binding and transcriptional efficacy of nuclear factor CREB.

TL;DR: Findings demonstrate that cellular signals can modulate gene expression by regulating the covalent modification of pre-existing nuclear factors.
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Cyclic AMP and the induction of eukaryotic gene transcription.

TL;DR: L'AMPc coordonne differentes voies metaboliques allant de la degradation du glycogene dans le foie des mammiferes a la synthese d'enzymes specifiques impliquees dansLe metabolisme energetique d'Escherichia coli.
References
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Journal ArticleDOI

Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

TL;DR: A procedure for preparing extracts from nuclei of human tissue culture cells that directs accurate transcription initiation in vitro from class II promoters, including tRNA and Ad 2 VA, is developed.
Journal ArticleDOI

Identification of a cyclic-AMP-responsive element within the rat somatostatin gene.

TL;DR: The studies indicate that transcriptional regulation of the somatostatin gene by cAMP requires protein kinase 2 activity and may depend upon a highly conserved promoter element.
Book ChapterDOI

Transcription maps of polyoma virus-specific RNA: analysis by two-dimensional nuclease S1 gel mapping.

TL;DR: This chapter describes the analysis of transcription maps of polyoma virus-specific RNA by 2-D nuclease S1 gel mapping and the standard procedures used for the preparation of viral nucleic acids and hybridization probes.
Journal ArticleDOI

Interaction of a gene-specific transcription factor with the adenovirus major late promoter upstream of the TATA box region

TL;DR: Dissociation rate measurements indicate a cooperative interaction between USF and TFIID when simultaneously bound to the promoter DNA.
Journal ArticleDOI

An adenovirus type 5 early gene function regulates expression of other early viral genes

TL;DR: An adenovirus type 5(Ad5) early gene function located in early region 1 which is required for the production of early cytoplasmic mRNAs corresponding to early regions 2, 3, and 4 is identified.
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