Evidence map›Paper›PMID 26755556›Full record

ArticleMolecular and cellular biology2016

The INO80 Complex Requires the Arp5-Ies6 Subcomplex for Chromatin Remodeling and Metabolic Regulation.

Wei Yao, Devin A King, Sean L Beckwith, Graeme J Gowans, Kuangyu Yen, Coral Zhou, Ashby J Morrison

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.5field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 60 citations in OpenAlex.

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  7. Envisioning a role for nuclear actin in prophase I spermatocytes.Frontiers in cell and developmental biology · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Wei YaoDepartment of Biology, Stanford University, Stanford, California, USA.
Devin A KingDepartment of Biology, Stanford University, Stanford, California, USA.
Sean L BeckwithDepartment of Biology, Stanford University, Stanford, California, USA.
Graeme J GowansDepartment of Biology, Stanford University, Stanford, California, USA.
Kuangyu YenDepartment of Cell Biology, Southern Medical University, Guangzhou, China Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, Pennsylvania, USA.
Coral ZhouDepartment of Biochemistry and Biophysics, University of California at San Francisco, San Francisco, California, USA.
Ashby J MorrisonDepartment of Biology, Stanford University, Stanford, California, USA ashbym@stanford.edu.ORCID http://orcid.org/0000-0003-1228-5093
Stanford University · USPennsylvania State University · USUniversity of California, San Francisco · US

Funding

INSTITUTIONAL TRAINING GRANT IN GENOME SCIENCET32HG000044 · NHGRI · STANFORD UNIVERSITY · PI MICHAEL P. SNYDER · 1995 to 2026
$32.2M
Chromatin-modifying functions of INO80 in the preservation of genomic integrityR00GM085212 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 2009 to 2011
$784k
Chromatin-modifying functions of INO80 in the preservation of genomic integrityK99GM085212 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MORRISON, ASHBY J. · 2008 to 2008
$90k
NHGRI NIH HHS T32 HG000044NIGMS NIH HHS GM085212
6 · The paper itself

Abstract

ATP-dependent chromatin remodeling complexes are essential for transcription regulation, and yet it is unclear how these multisubunit complexes coordinate their activities to facilitate diverse transcriptional responses. In this study, we found that the conserved Arp5 and Ies6 subunits of the Saccharomyces cerevisiae INO80 chromatin-remodeler form an abundant and distinct subcomplex in vivo and stimulate INO80-mediated activity in vitro. Moreover, our genomic studies reveal that the relative occupancy of Arp5-Ies6 correlates with nucleosome positioning at transcriptional start sites and expression levels of >1,000 INO80-regulated genes. Notably, these genes are significantly enriched in energy metabolism pathways. Specifically, arp5Δ, ies6Δ, and ino80Δ mutants demonstrate decreased expression of genes involved in glycolysis and increased expression of genes in the oxidative phosphorylation pathway. Deregulation of these metabolic pathways results in constitutively elevated mitochondrial potential and oxygen consumption. Our results illustrate the dynamic nature of the INO80 complex assembly and demonstrate for the first time that a chromatin remodeler regulates glycolytic and respiratory capacity, thereby maintaining metabolic stability.

Indexed as

Chromatin Assembly and DisassemblyMetabolic Networks and PathwaysChromosomal Proteins, Non-HistoneGene DeletionGene Expression Regulation, FungalGene Regulatory NetworksSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsArp5 protein, S cerevisiaeChromosomal Proteins, Non-HistoneIes6 protein, S cerevisiaeINO80 complex, S cerevisiaeSaccharomyces cerevisiae Proteins

Identifiers

PMID26755556
PMCPMC4810468
OpenAlexW2238278349

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.