The repressing and enhancing functions of the herpes simplex virus regulatory protein ICP27 map to C-terminal regions and are required to modulate viral gene expression very early in infection (Q36810975)

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scientific article published on July 1990

Language	Label	Description	Also known as
English	The repressing and enhancing functions of the herpes simplex virus regulatory protein ICP27 map to C-terminal regions and are required to modulate viral gene expression very early in infection	scientific article published on July 1990

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

The repressing and enhancing functions of the herpes simplex virus regulatory protein ICP27 map to C-terminal regions and are required to modulate viral gene expression very early in infection (English)

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

author name string

L McMahan

1

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

P A Schaffer

2

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

language of work or name

0 references

publication date

1 July 1990

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Journal of Virology

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

64

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

7

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

3471-3485

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells

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Characterization of the herpes simplex virion-associated factor responsible for the induction of alpha genes.

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Fine-structure mapping and functional analysis of temperature-sensitive mutants in the gene encoding the herpes simplex virus type 1 immediate early protein VP175

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

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Regulation of herpesvirus macromolecular synthesis. I. Cascade regulation of the synthesis of three groups of viral proteins

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Activities of herpes simplex virus type 1 (HSV-1) ICP4 genes specifying nonsense peptides

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Regulation of the herpes simplex virus type 1 late (gamma 2) glycoprotein C gene: sequences between base pairs -34 to +29 control transient expression and responsiveness to transactivation by the products of the immediate early (alpha) 4 and 0 genes

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Deletion mutants in the gene encoding the herpes simplex virus type 1 immediate-early protein ICP0 exhibit impaired growth in cell culture

1 reference

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Activation of immediate-early, early, and late promoters by temperature-sensitive and wild-type forms of herpes simplex virus type 1 protein ICP4

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Complete DNA sequence of the short repeat region in the genome of herpes simplex virus type 1.

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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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Isolation and characterization of deletion mutants of herpes simplex virus type 1 in the gene encoding immediate-early regulatory protein ICP4.

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Identification of immediate early genes from herpes simplex virus that transactivate the virus thymidine kinase gene

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Herpes simplex virus type 1 ICP27 is an essential regulatory protein.

1 reference

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Stimulation of expression of a herpes simplex virus DNA-binding protein by two viral functions

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Evidence for a direct role for both the 175,000- and 110,000-molecular-weight immediate-early proteins of herpes simplex virus in the transactivation of delayed-early promoters

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Multiple functional domains in the adenovirus E1A gene

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The herpes simplex virus type 1 alpha protein ICP27 can act as a trans-repressor or a trans-activator in combination with ICP4 and ICP0.

1 reference

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Gene-specific transactivation by herpes simplex virus type 1 alpha protein ICP27.

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The complete DNA sequence of the long unique region in the genome of herpes simplex virus type 1.

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Conservation of gene organization in the lymphotropic herpesviruses herpesvirus Saimiri and Epstein-Barr virus

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Physical and functional domains of the herpes simplex virus transcriptional regulatory protein ICP4.

1 reference

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The regions important for the activator and repressor functions of herpes simplex virus type 1 alpha protein ICP27 map to the C-terminal half of the molecule

1 reference

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Herpes simplex virus type 1 ICP0 plays a critical role in the de novo synthesis of infectious virus following transfection of viral DNA.

1 reference

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Herpes simplex virus alpha protein ICP27 possesses separable positive and negative regulatory activities

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Herpes simplex virus type 1 ICP27 deletion mutants exhibit altered patterns of transcription and are DNA deficient

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

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Regulation of herpesvirus macromolecular synthesis. VIII. The transcription program consists of three phases during which both extent of transcription and accumulation of RNA in the cytoplasm are regulated

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Control of herpes simplex virus type 1 mRNA synthesis in cells infected with wild-type virus or the temperature-sensitive mutant tsK

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Collaborative complementation study of temperature-sensitive mutants of herpes simplex virus types 1 and 2

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Temporal regulation of herpes simplex virus type 1 transcription: location of transcripts on the viral genome

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Regulation of herpesvirus macromolecular synthesis V. Properties of α polypeptides made in HSV-1 and HSV-2 infected cells

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Evidence that herpes simplex virus DNA is transcribed by cellular RNA polymerase B

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Regulation of herpesvirus macromolecular synthesis: sequential transition of polypeptide synthesis requires functional viral polypeptides

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Viral DNA synthesis is required for the efficient expression of specific herpes simplex virus type 1 mRNA species

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Identification of herpes simplex virus DNA sequences which encode a trans-acting polypeptide responsible for stimulation of immediate early transcription

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Genetic relations between varicella-zoster virus and Epstein-Barr virus

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Isolation and characterization of a herpes simplex virus type 1 mutant containing a deletion within the gene encoding the immediate early polypeptide Vmw110.

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The products of herpes simplex virus type 1 (HSV-1) immediate early genes 1, 2 and 3 can activate HSV-1 gene expression in trans

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Regulation of herpes simplex virus 1 genes: alpha gene sequence requirements for transient induction of indicator genes regulated by beta or late (gamma 2) promoters

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Sequence determination and genetic content of the short unique region in the genome of herpes simplex virus type 1.

1 reference

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Promoter sequence and cell type can dramatically affect the efficiency of transcriptional activation induced by herpes simplex virus type 1 and its immediate-early gene products Vmw175 and Vmw110.

1 reference

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The DNA sequences of the long repeat region and adjoining parts of the long unique region in the genome of herpes simplex virus type 1.

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The DNA-binding properties of the major regulatory protein alpha 4 of herpes simplex viruses

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Herpes simplex virus alpha protein ICP27 can inhibit or augment viral gene transactivation

1 reference

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The herpes simplex virus type 1 immediate-early protein ICP27 is obligately required for the accumulation of a cellular protein during viral infection

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An adenovirus E1a protein region required for transformation and transcriptional repression

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Mutational dissection of the HSV-1 immediate-early protein Vmw175 involved in transcriptional transactivation and repression

1 reference

https://pubmed.ncbi.nlm.nih.gov/2161950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcription of herpes simplex type 1 DNA in nuclei isolated from infected HEp-2 and KB cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/2161950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Properties of herpesvirus-induced “immediate early” polypeptides

1 reference

https://pubmed.ncbi.nlm.nih.gov/2161950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/JVI.64.7.3471-3485.1990

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

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