Identification of the Sin3-binding site in Ume6 defines a two-step process for conversion of Ume6 from a transcriptional repressor to an activator in yeast.
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Signaling disrupts mSin3A binding to the Mad1-like Sin3-interacting domain of TIEG2, an Sp1-like repressorHigh-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disordersE2F mediates cell cycle-dependent transcriptional repression in vivo by recruitment of an HDAC1/mSin3B corepressor complexThe Sum1/Ndt80 transcriptional switch and commitment to meiosis in Saccharomyces cerevisiaeRegulation of entry into gametogenesisCyclophilin A is localized to the nucleus and controls meiosis in Saccharomyces cerevisiae.Oxidative stress-activated zinc cluster protein Stb5 has dual activator/repressor functions required for pentose phosphate pathway regulation and NADPH production.Raf60, a novel component of the Rpd3 histone deacetylase complex required for Rpd3 activity in Saccharomyces cerevisiae.Ime1 and Ime2 are required for pseudohyphal growth of Saccharomyces cerevisiae on nonfermentable carbon sourcesUme6 transcription factor is part of a signaling cascade that regulates autophagy.Interplay between chromatin and trans-acting factors on the IME2 promoter upon induction of the gene at the onset of meiosisSUB1 Plays a Negative Role during Starvation Induced Sporulation Program in Saccharomyces cerevisiae.Direct role for the Rpd3 complex in transcriptional induction of the anaerobic DAN/TIR genes in yeastMolecular genetic analysis of the yeast repressor Rfx1/Crt1 reveals a novel two-step regulatory mechanism.Genetic evidence for a SPO1-dependent signaling pathway controlling meiotic progression in yeast.Meiosis-specific destruction of the Ume6p repressor by the Cdc20-directed APC/CMultiple histone deacetylases are recruited by corepressor Sin3 and contribute to gene repression mediated by Opi1 regulator of phospholipid biosynthesis in the yeast Saccharomyces cerevisiae.HBP1 and Mad1 repressors bind the Sin3 corepressor PAH2 domain with opposite helical orientationsDSIF and RNA polymerase II CTD phosphorylation coordinate the recruitment of Rpd3S to actively transcribed genesThe Ume6 regulon coordinates metabolic and meiotic gene expression in yeastThe Sin3p PAH domains provide separate functions repressing meiotic gene transcription in Saccharomyces cerevisiae.Sporulation in the budding yeast Saccharomyces cerevisiae.Faithful modeling of transient expression and its application to elucidating negative feedback regulationThe family feud: turning off Sp1 by Sp1-like KLF proteins.The MAPKKKs Ste11 and Bck1 jointly transduce the high oxidative stress signal through the cell wall integrity MAP kinase pathwayThe Zap1 transcriptional activator also acts as a repressor by binding downstream of the TATA box in ZRT2Sin3: master scaffold and transcriptional corepressor.Glucose and nitrogen regulate the switch from histone deacetylation to acetylation for expression of early meiosis-specific genes in budding yeast.Molecular characterization of Sin3 PAH-domain interactor specificity and identification of PAH partners.Ume6 is required for the MATa/MATalpha cellular identity and transcriptional silencing in Kluyveromyces lactis.Functional analysis of the Mad1-mSin3A repressor-corepressor interaction reveals determinants of specificity, affinity, and transcriptional response.Mixed Integer Linear Programming based machine learning approach identifies regulators of telomerase in yeast.Histone Deacetylases with Antagonistic Roles in Saccharomyces cerevisiae Heterochromatin Formation.How the Rgt1 transcription factor of Saccharomyces cerevisiae is regulated by glucose.Kinetochore inactivation by expression of a repressive mRNA.Mechanism for fetal hemoglobin induction by histone deacetylase inhibitors involves gamma-globin activation by CREB1 and ATF-2.Glucose-mediated phosphorylation converts the transcription factor Rgt1 from a repressor to an activator.Ume1p represses meiotic gene transcription in Saccharomyces cerevisiae through interaction with the histone deacetylase Rpd3p.One-two punch mechanism of gene repression: a fresh perspective on gene regulation.Transcriptional and post-transcriptional regulation of autophagy in the yeast Saccharomyces cerevisiae.
P2860
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P2860
Identification of the Sin3-binding site in Ume6 defines a two-step process for conversion of Ume6 from a transcriptional repressor to an activator in yeast.
description
2001 nî lūn-bûn
@nan
2001 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի մարտին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Identification of the Sin3-bin ...... ssor to an activator in yeast.
@ast
Identification of the Sin3-bin ...... ssor to an activator in yeast.
@en
type
label
Identification of the Sin3-bin ...... ssor to an activator in yeast.
@ast
Identification of the Sin3-bin ...... ssor to an activator in yeast.
@en
prefLabel
Identification of the Sin3-bin ...... ssor to an activator in yeast.
@ast
Identification of the Sin3-bin ...... ssor to an activator in yeast.
@en
P2860
P1476
Identification of the Sin3-bin ...... ssor to an activator in yeast.
@en
P2093
B K Washburn
R E Esposito
P2860
P304
P356
10.1128/MCB.21.6.2057-2069.2001
P407
P577
2001-03-01T00:00:00Z