Glucose and nitrogen regulate the switch from histone deacetylation to acetylation for expression of early meiosis-specific genes in budding yeast. - Wikidata - awgldk - TriplyDB

Glucose and nitrogen regulate the switch from histone deacetylation to acetylation for expression of early meiosis-specific genes in budding yeast.

Glucose and nitrogen regulate the switch from histone deacetylation to acetylation for expression of early meiosis-specific genes in budding yeast.

http://www.wikidata.org/entity/Q39380154

about

Gene expression analysis reveals that histone deacetylation sites may serve as partitions of chromatin gene expression domains.Nutritional control of growth and development in yeast Regulation of entry into gametogenesis Control of relative timing and stoichiometry by a master regulator The roles of the catalytic and noncatalytic activities of Rpd3L and Rpd3S in the regulation of gene transcription in yeast Ume6 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 meiosis Meiosis-specific destruction of the Ume6p repressor by the Cdc20-directed APC/C Dissecting the gene network of dietary restriction to identify evolutionarily conserved pathways and new functional genes.Multiple MAPK cascades regulate the transcription of IME1, the master transcriptional activator of meiosis in Saccharomyces cerevisiae The Rim15-endosulfine-PP2ACdc55 signalling module regulates entry into gametogenesis and quiescence via distinct mechanisms in budding yeast.Causal variation in yeast sporulation tends to reside in a pathway bottleneck Faithful modeling of transient expression and its application to elucidating negative feedback regulation Gcn5p-dependent acetylation induces degradation of the meiotic transcriptional repressor Ume6p Nutrient Control of Yeast Gametogenesis Is Mediated by TORC1, PKA and Energy Availability Rim15 and the crossroads of nutrient signalling pathways in Saccharomyces cerevisiae.How to halve ploidy: lessons from budding yeast meiosis.A Computational Approach to Study Gene Expression Networks.The in vivo activity of Ime1, the key transcriptional activator of meiosis-specific genes in Saccharomyces cerevisiae, is inhibited by the cyclic AMP/protein kinase A signal pathway through the glycogen synthase kinase 3-beta homolog Rim11.The chromatin remodeling complex Swi/Snf regulates splicing of meiotic transcripts in Saccharomyces cerevisiae.Functional dissection of IME1 transcription using quantitative promoter-reporter screening.The transcription activity of Gis1 is negatively modulated by proteasome-mediated limited proteolysis.

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Glucose and nitrogen regulate the switch from histone deacetylation to acetylation for expression of early meiosis-specific genes in budding yeast.

http://www.wikidata.org/entity/Q39380154

description

2004 nî lūn-bûn

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2004年の論文

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年學術文章

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2004年學術文章

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2004年學術文章

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name

Glucose and nitrogen regulate ...... ecific genes in budding yeast.

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Glucose and nitrogen regulate ...... ecific genes in budding yeast.

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type

label

Glucose and nitrogen regulate ...... ecific genes in budding yeast.

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Glucose and nitrogen regulate ...... ecific genes in budding yeast.

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prefLabel

Glucose and nitrogen regulate ...... ecific genes in budding yeast.

@en

Glucose and nitrogen regulate ...... ecific genes in budding yeast.

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MCB.24.12.5197-5208.2004

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Molecular and Cellular Biology

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Glucose and nitrogen regulate ...... ecific genes in budding yeast.

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Iris Edry

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Lilach Pnueli

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Miriam Cohen

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Yona Kassir

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P2860

Saccharomyces cerevisiae cAMP-dependent protein kinase controls entry into stationary phase through the Rim15p protein kinase.

Interaction of yeast repressor-activator protein Ume6p with glycogen synthase kinase 3 homolog Rim11p

Genetic evidence for transcriptional activation by the yeast IME1 gene product

UME6, a negative regulator of meiosis in Saccharomyces cerevisiae, contains a C-terminal Zn2Cys6 binuclear cluster that binds the URS1 DNA sequence in a zinc-dependent manner.

Ordered recruitment of transcription and chromatin remodeling factors to a cell cycle- and developmentally regulated promoter.

UME6 is a key regulator of nitrogen repression and meiotic development.

Identification of the Saccharomyces cerevisiae genes STB1-STB5 encoding Sin3p binding proteins.

SIR2 and SIR4 interactions differ in core and extended telomeric heterochromatin in yeast.

Repression by Ume6 involves recruitment of a complex containing Sin3 corepressor and Rpd3 histone deacetylase to target promoters.

Saccharomyces cerevisiae Ras/cAMP pathway controls post-diauxic shift element-dependent transcription through the zinc finger protein Gis1.

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5197-5208

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10.1128/MCB.24.12.5197-5208.2004

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