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Molecular genetic analysis of the yeast repressor Rfx1/Crt1 reveals a novel two-step regulatory mechanism
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scholarly article
1 reference
stated in
PubMed
PubMed ID
16107689
retrieved
1 December 2016
title
Molecular genetic analysis of the yeast repressor Rfx1/Crt1 reveals a novel two-step regulatory mechanism
(English)
1 reference
stated in
PubMed
PubMed ID
16107689
retrieved
1 December 2016
main subject
cell biology
0 references
Rfx1p YLR176C
1 reference
stated in
GOA release 2020-03-11
author name string
Zhengjian Zhang
series ordinal
1
0 references
Joseph C Reese
series ordinal
2
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language of work or name
English
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publication date
September 2005
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published in
Molecular and Cellular Biology
1 reference
stated in
PubMed
PubMed ID
16107689
retrieved
1 December 2016
volume
25
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issue
17
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page(s)
7399-411
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ImageQuant
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stated in
Europe PubMed Central
retrieved
11 June 2022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/PMC1190298/fullTextXML
based on heuristic
inferred from PubMed Central ID database lookup
cites work
Redundant mechanisms are used by Ssn6-Tup1 in repressing chromosomal gene transcription in Saccharomyces cerevisiae
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PubMed Central
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Ssn6-Tup1 requires the ISW2 complex to position nucleosomes in Saccharomyces cerevisiae
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PubMed Central
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Tup1-Ssn6 interacts with multiple class I histone deacetylases in vivo.
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SWI/SNF-dependent chromatin remodeling of RNR3 requires TAF(II)s and the general transcription machinery
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Hog1 kinase converts the Sko1-Cyc8-Tup1 repressor complex into an activator that recruits SAGA and SWI/SNF in response to osmotic stress
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Cti6, a PHD domain protein, bridges the Cyc8-Tup1 corepressor and the SAGA coactivator to overcome repression at GAL1.
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TUP1 utilizes histone H3/H2B-specific HDA1 deacetylase to repress gene activity in yeast
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Srb7p is a physical and physiological target of Tup1p
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PubMed Central
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Ssn6-Tup1 interacts with class I histone deacetylases required for repression
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PubMed Central
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Tup1p represses Mcm1p transcriptional activation and chromatin remodeling of an a-cell-specific gene
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Hrs1/Med3 is a Cyc8-Tup1 corepressor target in the RNA polymerase II holoenzyme.
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NORF5/HUG1 is a component of the MEC1-mediated checkpoint response to DNA damage and replication arrest in Saccharomyces cerevisiae
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Dimeric RFX proteins contribute to the activity and lineage specificity of the interleukin-5 receptor alpha promoter through activation and repression domains
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The DNA replication and damage checkpoint pathways induce transcription by inhibition of the Crt1 repressor
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Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae
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Repression domain of the yeast global repressor Tup1 interacts directly with histones H3 and H4.
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Induction of meiosis in Saccharomyces cerevisiae depends on conversion of the transcriptional represssor Ume6 to a positive regulator by its regulated association with the transcriptional activator Ime1.
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The DNA damage response: putting checkpoints in perspective
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The coregulator exchange in transcriptional functions of nuclear receptors
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The RFX family interacts at the collagen (COL1A2) start site and represses transcription
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Winged helix proteins
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ATP-dependent mobilization of the glucocorticoid receptor during chromatin remodeling
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The organized chromatin domain of the repressed yeast a cell-specific gene STE6 contains two molecules of the corepressor Tup1p per nucleosome
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29 September 2017
Assays for nucleosome positioning in yeast
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29 September 2017
DNA damage and cell cycle regulation of ribonucleotide reductase
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29 September 2017
Chromatin-mediated transcriptional repression in yeast
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29 September 2017
A eukaryotic transcriptional activator bearing the DNA specificity of a prokaryotic repressor
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29 September 2017
Characterization of TUP1, a mediator of glucose repression in Saccharomyces cerevisiae
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29 September 2017
In vivo footprinting of rat TAT gene: Dynamic interplay between the glucocorticoid receptor and a liver-specific factor
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29 September 2017
Isolation of crt mutants constitutive for transcription of the DNA damage inducible gene RNR3 in Saccharomyces cerevisiae
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29 September 2017
Cell type-specific chromatin organization of the region that governs directionality of yeast mating type switching
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2 June 2018
The global transcriptional regulators, SSN6 and TUP1, play distinct roles in the establishment of a repressive chromatin structure.
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2 June 2018
Cloning and characterization of the CYC8 gene mediating glucose repression in yeast
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2 June 2018
Highly specific antibodies determine histone acetylation site usage in yeast heterochromatin and euchromatin
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27 November 2018
Ssn6-Tup1 regulates RNR3 by positioning nucleosomes and affecting the chromatin structure at the upstream repression sequence.
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27 November 2018
The dimerization/repression domain of RFX1 is related to a conserved region of its yeast homologues Crt1 and Sak1: a new function for an ancient motif.
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27 November 2018
Mapping DNA interaction sites of chromosomal proteins using immunoprecipitation and polymerase chain reaction.
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27 November 2018
Co-activators and co-repressors in the integration of transcriptional responses
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27 November 2018
Transcription activation in cells lacking TAFIIS.
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27 November 2018
Transcriptional repression directed by the yeast alpha 2 protein in vitro
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27 November 2018
Yeast TAFIIS in a multisubunit complex required for activated transcription.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1190298
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27 November 2018
Recruitment of the yeast Tup1p-Ssn6p repressor is associated with localized decreases in histone acetylation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16107689
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1128/MCB.25.17.7399-7411.2005
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1433520
OpenCitations bibliographic resource ID
1433520
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1433520
PMCID
1190298
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1433520
PubMed ID
16107689
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1433520
ResearchGate publication ID
7652372
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