The genome-wide localization of Rsc9, a component of the RSC chromatin-remodeling complex, changes in response to stress (Q27935491)

PubMed

1 December 2016

title

The genome-wide localization of Rsc9, a component of the RSC chromatin-remodeling complex, changes in response to stress (English)

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PubMed

1 December 2016

1 reference

GOA release 2020-03-11

Rsc8p YFR037C

1 reference

GOA release 2020-03-11

Rsc6p YCR052W

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GOA release 2020-03-11

author

Paul Tempst

6

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Itamar Simon

Itamar Simon

2

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Frederick P. Roth

Frederick P Roth

7

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Pamela Silver

10

Pamela A Silver

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Richard A. Young

8

Richard A Young

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author name string

Marc Damelin

1

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Terence I Moy

3

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Boris Wilson

4

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Suzanne Komili

5

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Bradley R Cairns

9

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publication date

March 2002

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language of work or name

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1 reference

Basic local alignment search tool

1 December 2016

volume

9

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issue

3

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page(s)

563-73

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cites work

1 reference

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A Rsc3/Rsc30 zinc cluster dimer reveals novel roles for the chromatin remodeler RSC in gene expression and cell cycle control

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The TOR signalling pathway controls nuclear localization of nutrient-regulated transcription factors

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RSC, an essential, abundant chromatin-remodeling complex

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7 January 2021

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7 January 2021

Two functionally distinct forms of the RSC nucleosome-remodeling complex, containing essential AT hook, BAH, and bromodomains

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Sfh1p, a component of a novel chromatin-remodeling complex, is required for cell cycle progression

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The TOR signaling cascade regulates gene expression in response to nutrients

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Remodeling of yeast genome expression in response to environmental changes

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A chemical genomics approach toward understanding the global functions of the target of rapamycin protein (TOR).

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

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YPD, PombePD and WormPD: model organism volumes of the BioKnowledge library, an integrated resource for protein information

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Cluster analysis and display of genome-wide expression patterns

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Genome-wide responses to mitochondrial dysfunction

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Genomic expression programs in the response of yeast cells to environmental changes

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Characterization of the dead ringer gene identifies a novel, highly conserved family of sequence-specific DNA-binding proteins

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Rapamycin-modulated transcription defines the subset of nutrient-sensitive signaling pathways directly controlled by the Tor proteins

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The immunoglobulin heavy-chain matrix-associating regions are bound by Bright: a B cell-specific trans-activator that describes a new DNA-binding protein family

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Solution structure of the DNA binding domain from Dead ringer, a sequence-specific AT-rich interaction domain (ARID)

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Genomic binding sites of the yeast cell-cycle transcription factors SBF and MBF

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Eukaryotic Transcription: An Interlaced Network of Transcription Factors and Chromatin-Modifying Machines

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ATP-dependent remodeling and acetylation as regulators of chromatin fluidity

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An essential Saccharomyces cerevisiae gene homologous to SNF2 encodes a helicase-related protein in a new family

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Transcriptional repression of the yeast CHA1 gene requires the chromatin-remodeling complex RSC.

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Two microtubule-associated proteins required for anaphase spindle movement in Saccharomyces cerevisiae

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Regulation of ribosome biogenesis by the rapamycin-sensitive TOR-signaling pathway in Saccharomyces cerevisiae

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Genome-wide location and function of DNA binding proteins

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Signaling and circuitry of multiple MAPK pathways revealed by a matrix of global gene expression profiles

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The TOR kinases link nutrient sensing to cell growth

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A Saccharomyces cerevisiae genomic plasmid bank based on a centromere-containing shuttle vector

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TOR, a central controller of cell growth

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Interactions between a nuclear transporter and a subset of nuclear pore complex proteins depend on Ran GTPase

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Partitioning the transcriptional program induced by rapamycin among the effectors of the Tor proteins

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Factors affecting nuclear export of the 60S ribosomal subunit in vivo

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Interaction of a Swi3 homolog with Sth1 provides evidence for a Swi/Snf-related complex with an essential function in Saccharomyces cerevisiae

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Nps1/Sth1p, a component of an essential chromatin-remodeling complex of Saccharomyces cerevisiae, is required for the maximal expression of early meiotic genes

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7 January 2021

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PubMed