Evidence map›Paper›PMID 24315104›Full record

ArticleCell2013

Genome-wide map of nuclear protein degradation shows NCoR1 turnover as a key to mitochondrial gene regulation.

André Catic, Carol Y Suh, Cedric T Hill, Laurence Daheron, Theresa Henkel, Keith W Orford, David M Dombkowski, Tao Liu, X Shirley Liu, David T Scadden

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

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  15. Cellular Metabolism and Aging.Progress in molecular biology and translational science · 2018
    Review
  16. Article
  17. Nuclear Receptor Corepressor 1 Expression and Output Declines with Prostate Cancer Progression.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Article
  18. Review
  19. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 2 countries.

André CaticCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Stem Cell Institute, Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA. Electronic address: catic@post.harvard.edu.
Carol Y Suh
Cedric T Hill
Laurence Daheron
Theresa Henkel
Keith W Orford
David M Dombkowski
Tao Liu
X Shirley Liu
David T Scadden
Massachusetts General Hospital · USDana-Farber Cancer Institute · USHarvard Stem Cell Institute · USAustrian Academy of Sciences · ATHarvard University · US

Funding

FUNCTIONAL ISOLATION OF HUMAN HEMATOPOIETIC STEM CELLSR01DK050234 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI SCADDEN, DAVID T · 1995 to 2012
$3.7M
Computational Models for Mechanisms of Global Transcription RegulationR01HG004069 · NHGRI · DANA-FARBER CANCER INST · PI LIU, XIAOLE SHIRLEY · 2006 to 2013
$3.6M
Regulation of stem cell fate by protein degradationK01AG036744 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI CATIC, ANDRE · 2010 to 2014
$658k
NHGRI NIH HHS R01 HG004069NIA NIH HHS K01 AG036744NIA NIH HHS K01-AG036744NIDDK NIH HHS DK050234NIDDK NIH HHS R01 DK050234
6 · The paper itself

Abstract

Transcription factor activity and turnover are functionally linked, but the global patterns by which DNA-bound regulators are eliminated remain poorly understood. We established an assay to define the chromosomal location of DNA-associated proteins that are slated for degradation by the ubiquitin-proteasome system. The genome-wide map described here ties proteolysis in mammalian cells to active enhancers and to promoters of specific gene families. Nuclear-encoded mitochondrial genes in particular correlate with protein elimination, which positively affects their transcription. We show that the nuclear receptor corepressor NCoR1 is a key target of proteolysis and physically interacts with the transcription factor CREB. Proteasome inhibition stabilizes NCoR1 in a site-specific manner and restrains mitochondrial activity by repressing CREB-sensitive genes. In conclusion, this functional map of nuclear proteolysis links chromatin architecture with local protein stability and identifies proteolytic derepression as highly dynamic in regulating the transcription of genes involved in energy metabolism.

Indexed as

Gene Expression RegulationProteolysisRegulatory Elements, TranscriptionalAnimalsCyclic AMP Response Element-Binding ProteinGenome-Wide Association StudyHumansMiceMitochondriaNuclear Receptor Co-Repressor 1UbiquitinationCyclic AMP Response Element-Binding ProteinNCOR1 protein, humanNcor1 protein, mouseNuclear Receptor Co-Repressor 1

Identifiers

PMID24315104
PMCPMC4068507
OpenAlexW2073651235

What OpenQuestion holds

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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.