ATF6 activated by proteolysis binds in the presence of NF-Y (CBF) directly to the cis-acting element responsible for the mammalian unfolded protein response (Q28611502)

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English	ATF6 activated by proteolysis binds in the presence of NF-Y (CBF) directly to the cis-acting element responsible for the mammalian unfolded protein response	scientific journal article

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scholarly article

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3 February 2017

ATF6 activated by proteolysis binds in the presence of NF-Y (CBF) directly to the cis-acting element responsible for the mammalian unfolded protein response (English)

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3 February 2017

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based on heuristic

inferred from title

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ORCID Public Data File 2021

author name string

H. Yoshida

1

1 reference

3 February 2017

T. Okada

2

1 reference

3 February 2017

K. Haze

3

1 reference

3 February 2017

H. Yanagi

4

1 reference

3 February 2017

T. Yura

5

1 reference

3 February 2017

M. Negishi

6

1 reference

3 February 2017

K. Mori

7

1 reference

3 February 2017

language of work or name

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publication date

1 September 2000

1 reference

3 February 2017

Molecular and Cellular Biology

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3 February 2017

20

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3 February 2017

6755–6767

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3 February 2017

18

1 reference

3 February 2017

Perk is essential for translational regulation and cell survival during the unfolded protein response

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=86199

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An essential role in liver development for transcription factor XBP-1

1 reference

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Mammalian transcription factor ATF6 is synthesized as a transmembrane protein and activated by proteolysis in response to endoplasmic reticulum stress

1 reference

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Protein translation and folding are coupled by an endoplasmic-reticulum-resident kinase

1 reference

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CHOP-Dependent stress-inducible expression of a novel form of carbonic anhydrase VI

1 reference

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Identification of the cis-acting endoplasmic reticulum stress response element responsible for transcriptional induction of mammalian glucose-regulated proteins. Involvement of basic leucine zipper transcription factors

1 reference

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Cloning of mammalian Ire1 reveals diversity in the ER stress responses

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Identification of novel stress-induced genes downstream of chop

1 reference

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17 March 2017

A stress response pathway from the endoplasmic reticulum to the nucleus requires a novel bifunctional protein kinase/endoribonuclease (Ire1p) in mammalian cells

1 reference

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CHOP is implicated in programmed cell death in response to impaired function of the endoplasmic reticulum

1 reference

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17 March 2017

The transmembrane kinase Ire1p is a site-specific endonuclease that initiates mRNA splicing in the unfolded protein response

1 reference

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Interaction of ATF6 and serum response factor

1 reference

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Cloning and expression of human NF-YC

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Signalling from endoplasmic reticulum to nucleus: transcription factor with a basic-leucine zipper motif is required for the unfolded protein-response pathway

1 reference

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Homocysteine-respondent genes in vascular endothelial cells identified by differential display analysis. GRP78/BiP and novel genes

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tRNA ligase is required for regulated mRNA splicing in the unfolded protein response

1 reference

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A novel mechanism for regulating activity of a transcription factor that controls the unfolded protein response

1 reference

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The basic domain/leucine zipper protein hXBP-1 preferentially binds to and transactivates CRE-like sequences containing an ACGT core

1 reference

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Stress-induced binding of the transcriptional factor CHOP to a novel DNA control element

1 reference

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Transcriptional induction of genes encoding endoplasmic reticulum resident proteins requires a transmembrane protein kinase

1 reference

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A transmembrane protein with a cdc2+/CDC28-related kinase activity is required for signaling from the ER to the nucleus

1 reference

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A new member of the leucine zipper class of proteins that binds to the HLA DR alpha promoter

1 reference

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Multiple cDNA clones encoding nuclear proteins that bind to the tax-dependent enhancer of HTLV-1: all contain a leucine zipper structure and basic amino acid domain

1 reference

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Isolation of cDNAs for DNA-binding proteins which specifically bind to a tax-responsive enhancer element in the long terminal repeat of human T-cell leukemia virus type I

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CHOP, a novel developmentally regulated nuclear protein that dimerizes with transcription factors C/EBP and LAP and functions as a dominant-negative inhibitor of gene transcription

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17 March 2017

Isolation, characterization and chromosomal localization of the human GADD153 gene

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17 March 2017

Dynamic interaction of BiP and ER stress transducers in the unfolded-protein response

1 reference

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7 April 2017

Stress signaling from the lumen of the endoplasmic reticulum: coordination of gene transcriptional and translational controls

1 reference

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7 April 2017

Protein folding in the cell

1 reference

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The presence of malfolded proteins in the endoplasmic reticulum signals the induction of glucose-regulated proteins

1 reference

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Tripartite management of unfolded proteins in the endoplasmic reticulum

1 reference

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mRNA splicing-mediated C-terminal replacement of transcription factor Hac1p is required for efficient activation of the unfolded protein response

1 reference

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Mechanism of non-spliceosomal mRNA splicing in the unfolded protein response pathway

1 reference

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The mammalian endoplasmic reticulum stress response element consists of an evolutionarily conserved tripartite structure and interacts with a novel stress-inducible complex

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Role of the CCAAT-binding protein CBF/NF-Y in transcription

1 reference

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Translational attenuation mediated by an mRNA intron

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Endoplasmic reticulum stress-induced mRNA splicing permits synthesis of transcription factor Hac1p/Ern4p that activates the unfolded protein response

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Saccharomyces cerevisiae IRE2/HAC1 is involved in IRE1-mediated KAR2 expression

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Calcium-sensitive transcriptional activation of the proximal CCAAT regulatory element of the grp78/BiP promoter by the human nuclear factor CBF/NF-Y.

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GADD153/CHOP, a DNA damage-inducible protein, reduced CAAT/enhancer binding protein activities and increased apoptosis in 32D c13 myeloid cells.

1 reference

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Signals from the stressed endoplasmic reticulum induce C/EBP-homologous protein (CHOP/GADD153).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=86199

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Transactivation of the grp78 promoter by Ca2+ depletion. A comparative analysis with A23187 and the endoplasmic reticulum Ca(2+)-ATPase inhibitor thapsigargin

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Regulation of the C/EBP-related gene gadd153 by glucose deprivation

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CHOP (GADD153) and its oncogenic variant, TLS-CHOP, have opposing effects on the induction of G1/S arrest.

1 reference

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Stress induction of the mammalian GRP78/BiP protein gene: in vivo genomic footprinting and identification of p70CORE from human nuclear extract as a DNA-binding component specific to the stress regulatory element

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Mammalian genes coordinately regulated by growth arrest signals and DNA-damaging agents

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Transactivation of the grp78 promoter by malfolded proteins, glycosylation block, and calcium ionophore is mediated through a proximal region containing a CCAAT motif which interacts with CTF/NF-I

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A 22 bp cis-acting element is necessary and sufficient for the induction of the yeast KAR2 (BiP) gene by unfolded proteins

1 reference

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1 reference

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inferred from PubMed ID database lookup

Unconventional splicing of HAC1/ERN4 mRNA required for the unfolded protein response. Sequence-specific and non-sequential cleavage of the splice sites

1 reference

https://pubmed.ncbi.nlm.nih.gov/10958673

12 December 2020

based on heuristic

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Normal fibroblasts induce the C/EBP beta and ATF-4 bZIP transcription factors in response to anoxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/10958673

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based on heuristic

inferred from PubMed ID database lookup

The endoplasmic reticulum as a protein-folding compartment

1 reference

https://pubmed.ncbi.nlm.nih.gov/10958673

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based on heuristic

inferred from PubMed ID database lookup

A high-efficiency HeLa cell nuclear transcription extract

1 reference

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based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/MCB.20.18.6755-6767.2000

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24 November 2022

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

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