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Transcription activation by the adenovirus E1a protein
scientific article (publication date: 2 March 1989)
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scholarly article
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title
Transcription activation by the adenovirus E1a protein
(English)
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PubMed
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30 April 2017
main subject
Adenoviridae
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author name string
Lillie JW
series ordinal
1
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30 April 2017
Green MR
series ordinal
2
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30 April 2017
language of work or name
English
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publication date
2 March 1989
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30 April 2017
published in
Nature
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reference URL
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30 April 2017
volume
338
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issue
6210
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PubMed
reference URL
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page(s)
39-44
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30 April 2017
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A eukaryotic transcriptional activator bearing the DNA specificity of a prokaryotic repressor
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Promoters, activator proteins, and the mechanism of transcriptional initiation in yeast
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How eukaryotic transcriptional activators work
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Fos-associated protein p39 is the product of the jun proto-oncogene
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The c-Fos protein interacts with c-Jun/AP-1 to stimulate transcription of AP-1 responsive genes
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fos-associated cellular p39 is related to nuclear transcription factor AP-1.
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Evidence of DNA: protein interactions that mediate HSV-1 immediate early gene activation by VP16.
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A complex formed between cell components and an HSV structural polypeptide binds to a viral immediate early gene regulatory DNA sequence
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Herpes simplex virus regulatory elements and the immunoglobulin octamer domain bind a common factor and are both targets for virion transactivation
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A herpesvirus trans-activating protein interacts with transcription factor OTF-1 and other cellular proteins
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Deletion analysis of GAL4 defines two transcriptional activating segments
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A new class of yeast transcriptional activators
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Functional dissection of a eukaryotic transcriptional activator protein, GCN4 of yeast
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Structural and functional characterization of the short acidic transcriptional activation region of yeast GCN4 protein
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Pre-early adenovirus 5 gene product regulates synthesis of early viral messenger RNAs
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An adenovirus type 5 early gene function regulates expression of other early viral genes
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Adenovirus promoters and E1A transactivation
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E1A 13S and 12S mRNA products made in Escherichia coli both function as nucleus-localized transcription activators but do not directly bind DNA
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Identification of a cellular transcription factor involved in E1A trans-activation.
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E1A transcription induction: enhanced binding of a factor to upstream promoter sequences
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Activation of a preexisting cellular factor as a basis for adenovirus E1A-mediated transcription control
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Factors responsible for the higher transcriptional activity of extracts of adenovirus-infected cells fractionate with the TATA box transcription factor
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Multiple functional domains in the adenovirus E1A gene
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Identification of separate domains in the adenovirus E1A gene for immortalization activity and the activation of virus early genes
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An adenovirus E1a protein region required for transformation and transcriptional repression
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An adenovirus E1A protein domain activates transcription in vivo and in vitro in the absence of protein synthesis
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Use of deletion and point mutants spanning the coding region of the adenovirus 5 E1A gene to define a domain that is essential for transcriptional activation
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The yeast UASG is a transcriptional enhancer in human HeLa cells in the presence of the GAL4 trans-activator
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GAL4-VP16 is an unusually potent transcriptional activator
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GAL4 activates gene expression in mammalian cells
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Functional dissection of VP16, the trans-activator of herpes simplex virus immediate early gene expression
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Crossref
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Signal transduction and transcriptional regulation by glucocorticoid receptor-LexA fusion proteins
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7 January 2021
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Multiple and cooperative trans-activation domains of the human glucocorticoid receptor
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DNA-bound Fos proteins activate transcription in yeast
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Crossref
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https://api.crossref.org/works/10.1038%2F338039A0
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7 January 2021
based on heuristic
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The 289-amino acid E1A protein of adenovirus binds zinc in a region that is important for trans-activation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F338039A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
A cellular protein, activating transcription factor, activates transcription of multiple E1A-inducible adenovirus early promoters
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2F338039A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Association of adenovirus early-region 1A proteins with cellular polypeptides
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2F338039A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of cellular proteins associated with human adenovirus type 5 early region 1A polypeptides.
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2F338039A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Activation of early adenovirus transcription by the herpesvirus immediate early gene: evidence for a common cellular control factor
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
HTLV-I tax induces cellular proteins that activate the kappa B element in the IL-2 receptor alpha gene
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2F338039A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Splicing of adenovirus 2 early region 1A mRNAs is non-sequential
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2F338039A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Adenovirus E1a proteins repress transcription from the SV40 early promoter
1 reference
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Crossref
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7 January 2021
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Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells
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Crossref
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https://api.crossref.org/works/10.1038%2F338039A0
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7 January 2021
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Identifiers
DOI
10.1038/338039A0
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stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=2521923
retrieved
30 April 2017
Dimensions Publication ID
1021771541
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PubMed ID
2521923
1 reference
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PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=2521923
retrieved
30 April 2017
Springer Nature article ID
10.1038/338039a0
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