(Q44455772)

English

Immediate early and functional AP-1 cis-response elements are involved in the transcriptional regulation of the large subunit of herpes simplex virus type 2 ribonucleotide reductase (ICP10)

scientific article published on May 1, 1992

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scholarly article

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Europe PubMed Central

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3 December 2017

Immediate early and functional AP-1 cis-response elements are involved in the transcriptional regulation of the large subunit of herpes simplex virus type 2 ribonucleotide reductase (ICP10) (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1320796

13 September 2022

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13 September 2022

cancer research

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10.1016/0168-1702(92)90112-M

https://api.crossref.org/works/10.1016/0168-1702(92)90112-M

6 December 2023

author name string

J. P. Wymer

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13 September 2022

C. M. Aprhys

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1320796

13 September 2022

T. D. Chung

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13 September 2022

C. P. Feng

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13 September 2022

M. Kulka

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13 September 2022

L. Aurelian

6

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13 September 2022

language of work or name

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National Center for Biotechnology Information

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1320796

13 September 2022

publication date

1 May 1992

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Europe PubMed Central

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3 December 2017

full work available at URL

https://api.elsevier.com/content/article/PII:016817029290112M?httpAccept=text/xml

1 reference

10.1016/0168-1702(92)90112-M

https://api.crossref.org/works/10.1016/0168-1702(92)90112-M

6 December 2023

https://api.elsevier.com/content/article/PII:016817029290112M?httpAccept=text/plain

1 reference

10.1016/0168-1702(92)90112-M

https://api.crossref.org/works/10.1016/0168-1702(92)90112-M

6 December 2023

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

23

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Europe PubMed Central

PubMed publication ID

3 December 2017

3

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Europe PubMed Central

PubMed publication ID

3 December 2017

253-270

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Characterization of Herpes Simplex Virus Type 1 RNA Present in the Absence of De Novo Protein Synthesis

1

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Oncogene jun encodes a sequence-specific trans-activator similar to AP-1.

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Overlapping octamer and TAATGARAT motifs in the VF65-response elements in herpes simplex virus immediate-early promoters represent independent binding sites for cellular nuclear factor III

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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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Myristylation and polylysine-mediated activation of the protein kinase domain of the large subunit of herpes simplex virus type 2 ribonucleotide reductase (ICP10).

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Leucine repeats in the large subunit of herpes simplex virus type 2 ribonucleotide reductase (RR; ICP10) are involved in RR activity and subunit complex formation

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Temperature-sensitive mutants in herpes simplex virus type 1 ICP4 permissive for early gene expression

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Expression of a truncated viral trans-activator selectively impedes lytic infection by its cognate virus

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Herpes simplex virus immediate-early promoters are responsive to virus and cell trans-acting factors

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A herpesvirus trans-activating protein interacts with transcription factor OTF-1 and other cellular proteins

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Factor(s) present in herpes simplex virus type 1-infected cells can compensate for the loss of the large subunit of the viral ribonucleotide reductase: characterization of an ICP6 deletion mutant

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The herpes simplex virus type 1 ribonucleotide reductase is a tight complex of the type alpha 2 beta 2 composed of 40K and 140K proteins, of which the latter shows multiple forms due to proteolysis

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A herpes simplex virus ribonucleotide reductase deletion mutant is defective for productive acute and reactivatable latent infections of mice and for replication in mouse cells

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The minimal transforming fragment of HSV-2 mtrIII can function as a complex promoter element

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Interactions of the Oct-1 POU subdomains with specific DNA sequences and with the HSV alpha-trans-activator protein

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Herpes simplex virus-infected cells contain a function(s) that destabilizes both host and viral mRNAs

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The Oct-2 protein binds cooperatively to adjacent octamer sites

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The 65,000-Mr DNA-binding and virion trans-inducing proteins of herpes simplex virus type 1.

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Expression of cloned herpesvirus genes. I. Detection of nuclear antigens from herpes simplex virus type 2 inverted repeat regions in transfected mouse cells

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Expression of recombinant genes containing herpes simplex virus delayed-early and immediate-early regulatory regions and trans activation by herpesvirus infection

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Three trans-acting regulatory proteins of herpes simplex virus modulate immediate-early gene expression in a pathway involving positive and negative feedback regulation

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Octamer transcription factors 1 and 2 each bind to two different functional elements in the immunoglobulin heavy-chain promoter

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10.1016/0168-1702(92)90112-M

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

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