Evidence map›Paper›PMID 19641020›Full record

ArticleMolecular biology of the cell2009

Heterogeneous nuclear ribonucleoprotein A2 is a common transcriptional coactivator in the nuclear transcription response to mitochondrial respiratory stress.

Manti Guha, Hua Pan, Ji-Kang Fang, Narayan G Avadhani

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

37 citing papers in PubMed, 55 citations in OpenAlex.

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  10. Revisiting the role of mitochondria in spinal muscular atrophy.Cellular and molecular life sciences : CMLS · 2021
    Review
  11. Article
  12. Article
  13. Esophageal 3D organoids ofOncotarget · 2019
    Article
  14. Review
  15. Article
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  17. Article
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  19. Mitochondrial dysfunction and mitochondrial dynamics-The cancer connection.Biochimica et biophysica acta. Bioenergetics · 2017
    Review
  20. Article
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

4 authors at 1 institution in 1 country.

Manti GuhaDepartment of Animal Biology and Marie Lowe Center for Comparative Oncology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Hua Pan
Ji-Kang Fang
Narayan G Avadhani
University of Pennsylvania · US

Funding

Role of Mitochondrial Respiratory Stress Signaling in Cancer ProgressionR01CA022762 · NCI · UNIVERSITY OF PENNSYLVANIA · PI AVADHANI, NARAYAN G · 1985 to 2013
$3.3M
MITOCHONDRIAL D-LOOP DNA MUTATIONS AND GENE EXPRESSIONR37CA022762 · NCI · UNIVERSITY OF PENNSYLVANIA · PI AVADHANI, NARAYAN G · 1994 to 2002
$299k
NCI NIH HHS CA-22762NCI NIH HHS R01 CA022762NCI NIH HHS R37 CA022762
6 · The paper itself

Abstract

Mitochondrial dysfunction and altered transmembrane potential initiate a mitochondrial respiratory stress response, also known as mitochondrial retrograde response, in a wide spectrum of cells. The mitochondrial stress response activates calcineurin, which regulates transcription factors, including a new nuclear factor-kappaB (NF-kappaB) pathway, different from the canonical and noncanonical pathways. In this study using a combination of small interfering RNA-mediated mRNA knock down, transcriptional analysis, and chromatin immunoprecipitation, we report a common mechanism for the regulation of previously established stress response genes Cathepsin L, RyR1, and Glut4. Stress-regulated transcription involves the cooperative interplay between NF-kappaB (cRel: p50), C/EBPdelta, cAMP response element-binding protein, and nuclear factor of activated T cells. We show that the functional synergy of these factors requires the stress-activated heterogeneous nuclear ribonucleoprotein (hnRNP) A2 as a coactivator. HnRNP A2 associates with the enhanceosome, mostly through protein-protein interactions with DNA-bound factors. Silencing of hnRNP A2 as well as other DNA binding signature factors prevents stress-induced transcriptional activation and reverses the invasiveness of mitochondrial DNA-depleted C2C12 cells. Induction of mitochondrial stress signaling by electron transfer chain inhibitors also involved hnRNPA2 activation. We describe a common mechanism of mitochondrial respiratory stress-induced activation of nuclear target genes that involves hnRNP A2 as a transcription coactivator.

Indexed as

Transcription, GeneticAnimalsCathepsin LCell NucleusCell RespirationGene SilencingGlucose Transporter Type 4Heterogeneous-Nuclear Ribonucleoprotein Group A-BHumansMiceMitochondriaModels, GeneticPromoter Regions, GeneticProtein BindingProtein Interaction MappingProtein Structure, TertiaryCathepsin LGlucose Transporter Type 4Heterogeneous-Nuclear Ribonucleoprotein Group A-BhnRNP A2Ryanodine Receptor Calcium Release ChannelTrans-Activators

Identifiers

PMID19641020
PMCPMC2743628
OpenAlexW2148123246

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.