Transcriptional activation and repression by Fos are independent functions: the C terminus represses immediate-early gene expression via CArG elements (Q36720751)

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scientific article published on August 1990

Language	Label	Description	Also known as
English	Transcriptional activation and repression by Fos are independent functions: the C terminus represses immediate-early gene expression via CArG elements	scientific article published on August 1990

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Transcriptional activation and repression by Fos are independent functions: the C terminus represses immediate-early gene expression via CArG elements (English)

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

immediate early gene

1 reference

based on heuristic

inferred from title

1 reference

ORCID Public Data File 2021

author name string

D Gius

1

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

X M Cao

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

F J Rauscher

3

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

D R Cohen

4

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

T Curran

5

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

V P Sukhatme

6

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

language of work or name

0 references

publication date

1 August 1990

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Molecular and Cellular Biology

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

10

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

8

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

4243-4255

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells

1 reference

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Molecular cloning of gene sequences regulated by platelet-derived growth factor.

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

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The biology and mechanism of action of nerve growth factor

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Stimulation of 3T3 cells induces transcription of the c-fos proto-oncogene

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Identification of a set of genes expressed during the G0/G1 transition of cultured mouse cells

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Mutation of the c-fos gene dyad symmetry element inhibits serum inducibility of transcription in vivo and the nuclear regulatory factor binding in vitro

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Cloning of tetradecanoyl phorbol ester-induced 'primary response' sequences and their expression in density-arrested Swiss 3T3 cells and a TPA non-proliferative variant

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Isolation and properties of cDNA clones encoding SRF, a transcription factor that binds to the c-fos serum response element

1 reference

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Induction of protooncogene c-jun by serum growth factors

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A gene inducible by serum growth factors encodes a member of the steroid and thyroid hormone receptor superfamily

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Activation of the transforming potential of the human fos proto-oncogene requires message stabilization and results in increased amounts of partially modified fos protein

1 reference

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Fos C-terminal mutations block down-regulation of c-fos transcription following serum stimulation.

1 reference

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c-Jun dimerizes with itself and with c-Fos, forming complexes of different DNA binding affinities

1 reference

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DNA binding activities of three murine Jun proteins: stimulation by Fos.

1 reference

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30 September 2017

The jun proto-oncogene is positively autoregulated by its product, Jun/AP-1

1 reference

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A gene activated in mouse 3T3 cells by serum growth factors encodes a protein with "zinc finger" sequences

1 reference

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1 reference

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5' flanking sequence and genomic structure of Egr-1, a murine mitogen inducible zinc finger encoding gene

1 reference

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The c-Fos protein interacts with c-Jun/AP-1 to stimulate transcription of AP-1 responsive genes

1 reference

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Two mouse genes encoding potential transcription factors with identical DNA-binding domains are activated by growth factors in cultured cells

1 reference

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30 September 2017

fra-1: a serum-inducible, cellular immediate-early gene that encodes a fos-related antigen.

1 reference

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Fos-associated protein p39 is the product of the jun proto-oncogene

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A gene encoding a protein with zinc fingers is activated during G0/G1 transition in cultured cells

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A zinc finger-encoding gene coregulated with c-fos during growth and differentiation, and after cellular depolarization

1 reference

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30 September 2017

Memories of fos.

1 reference

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Modification of fos proteins: phosphorylation of c-fos, but not v-fos, is stimulated by 12-tetradecanoyl-phorbol-13-acetate and serum

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CAT constructions with multiple unique restriction sites for the functional analysis of eukaryotic promoters and regulatory elements

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Avian sarcoma virus 17 carries the jun oncogene

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Multiple protein-binding sites in the 5'-flanking region regulate c-fos expression

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Induction of the proto-oncogene fos by nerve growth factor

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The role of the leucine zipper in the fos-jun interaction

1 reference

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Phosphorylation of serum response factor, a factor that binds to the serum response element of the c-FOS enhancer

1 reference

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1 reference

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Duplicated CArG box domains have positive and mutually dependent regulatory roles in expression of the human alpha-cardiac actin gene

1 reference

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The sarcomeric actin CArG-binding factor is indistinguishable from the c-fos serum response factor

1 reference

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Functional serum response elements upstream of the growth factor-inducible gene zif268

1 reference

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trans-repression of the mouse c-fos promoter: a novel mechanism of Fos-mediated trans-regulation.

1 reference

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30 September 2017

Autoregulation of fos: the dyad symmetry element as the major target of repression.

1 reference

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DNA binding site of the growth factor-inducible protein Zif268

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Two distinct cellular phosphoproteins bind to the c-fos serum response element

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The product of a novel growth factor activated gene, fos B, interacts with JUN proteins enhancing their DNA binding activity

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Transcriptional autoregulation of the proto-oncogene fos.

1 reference

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Induction of proto-oncogene JUN/AP-1 by serum and TPA.

1 reference

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The inner core of the serum response element mediates both the rapid induction and subsequent repression of c-fos transcription following serum stimulation

1 reference

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Induction of c-fos gene and protein by growth factors precedes activation of c-myc

1 reference

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Occupation of the c-fos serum response element in vivo by a multi-protein complex is unaltered by growth factor induction

1 reference

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1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcriptional activation of c-jun during the G0/G1 transition in mouse fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2115122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Negative regulation of serum-responsive enhancer elements

1 reference

https://pubmed.ncbi.nlm.nih.gov/2115122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid increase of an immediate early gene messenger RNA in hippocampal neurons by synaptic NMDA receptor activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2115122

12 December 2020

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Platelet-derived growth factor induces rapid but transient expression of the c-fos gene and protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/2115122

12 December 2020

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Nerve growth factor and epidermal growth factor induce rapid transient changes in proto-oncogene transcription in PC12 cells

1 reference

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12 December 2020

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1 reference

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inferred from PubMed ID database lookup

The Fos complex and Fos-related antigens recognize sequence elements that contain AP-1 binding sites

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Common DNA binding site for Fos protein complexesand transcription factor AP-1

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A novel early growth response gene rapidly induced by fibroblast, epithelial cell and lymphocyte mitogens

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Dynamic alterations occur in the levels and composition of transcription factor AP-1 complexes after seizure

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12 December 2020

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Structure-function analysis of fos protein: A single amino acid change activates the immortalizing potential of v-fos

1 reference

https://pubmed.ncbi.nlm.nih.gov/2115122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ability of a ternary complex to form over the serum response element correlates with serum inducibility of the human c-fos promoter

1 reference

https://pubmed.ncbi.nlm.nih.gov/2115122

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based on heuristic

inferred from PubMed ID database lookup

Parallel association of Fos and Jun leucine zippers juxtaposes DNA binding domains

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https://pubmed.ncbi.nlm.nih.gov/2115122

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based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/MCB.10.8.4243

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

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