Evidence map›Paper›PMID 27515817›Full record

ArticleFree radical biology & medicine2016

Novel RNA-binding activity of NQO1 promotes SERPINA1 mRNA translation.

Andrea Di Francesco, Clara Di Germanio, Amaresh C Panda, Phu Huynh, Robert Peaden, Ignacio Navas-Enamorado, Paul Bastian, Elin Lehrmann, Alberto Diaz-Ruiz, David Ross and 6 more

Open access · greenAbstract read
In one paragraph

Article in Free radical biology & medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  5. Article
  6. Impact of NQO1 dysregulation in CNS disorders.Journal of translational medicine · 2024
    Review
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  18. Zeta-crystallin: a moonlighting player in cancer.Cellular and molecular life sciences : CMLS · 2020
    Review
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  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

16 authors at 3 institutions in 1 country.

Andrea Di FrancescoExperimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA.
Clara Di GermanioExperimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA.
Amaresh C PandaRNA Regulation Section, Laboratory of Genetics and Genomics, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA.
Phu HuynhExperimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA.
Robert PeadenExperimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA.
Ignacio Navas-EnamoradoExperimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA.
Paul BastianRNA Regulation Section, Laboratory of Genetics and Genomics, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA.
Elin LehrmannRNA Regulation Section, Laboratory of Genetics and Genomics, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA.
Alberto Diaz-RuizExperimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA.
David RossDepartment of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado, Anschutz Medical Campus, 12858 East Montview Blvd., Aurora, CO 80045, USA.
David SiegelDepartment of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado, Anschutz Medical Campus, 12858 East Montview Blvd., Aurora, CO 80045, USA.
Jennifer L MartindaleRNA Regulation Section, Laboratory of Genetics and Genomics, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA.
Michel BernierExperimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA.
Myriam GorospeRNA Regulation Section, Laboratory of Genetics and Genomics, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA.
Kotb AbdelmohsenRNA Regulation Section, Laboratory of Genetics and Genomics, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA. Electronic address: abdelmohsenk@grc.nia.nih.gov.
Rafael de CaboExperimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, 251 Bayview Blvd., Suite 100, Baltimore, MD 21224, USA. Electronic address: deCaboRa@grc.nia.nih.gov.
National Institute on Aging · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Montana · US

Funding

Post-transcriptional regulation of energy usage: glucose and lipid metabolismZIAAG000394 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2025
$18.7M
NRF2 interactions with SIRT1 and its role on caloric restrictionZIAAG000361 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2009 to 2024
$5.3M
Aging and CR effects on the Plasma Membrane Redox SystemZIAAG000362 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2009 to 2025
$5.0M
Aging and CR effects on the Plasma Membrane Redox SystemZ01AG000362 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2008 to 2008
$422k
Intramural NIH HHS Z01 AG000362Intramural NIH HHS Z99 AG999999
6 · The paper itself

Abstract

NAD(P)H: quinone oxidoreductase (NQO1) is essential for cell defense against reactive oxidative species, cancer, and metabolic stress. Recently, NQO1 was found in ribonucleoprotein (RNP) complexes, but NQO1-interacting mRNAs and the functional impact of such interactions are not known. Here, we used ribonucleoprotein immunoprecipitation (RIP) and microarray analysis to identify comprehensively the subset of NQO1 target mRNAs in human hepatoma HepG2 cells. One of its main targets, SERPINA1 mRNA, encodes the serine protease inhibitor α-1-antitrypsin, A1AT, which is associated with disorders including obesity-related metabolic inflammation, chronic obstructive pulmonary disease (COPD), liver cirrhosis and hepatocellular carcinoma. Biotin pulldown analysis indicated that NQO1 can bind the 3' untranslated region (UTR) and the coding region (CR) of SERPINA1 mRNA. NQO1 did not affect SERPINA1 mRNA levels; instead, it enhanced the translation of SERPINA1 mRNA, as NQO1 silencing decreased the size of polysomes forming on SERPINA1 mRNA and lowered the abundance of A1AT. Luciferase reporter analysis further indicated that NQO1 regulates SERPINA1 mRNA translation through the SERPINA1 3'UTR. Accordingly, NQO1-KO mice had reduced hepatic and serum levels of A1AT and increased activity of neutrophil elastase (NE), one of the main targets of A1AT. We propose that this novel mechanism of action of NQO1 as an RNA-binding protein may help to explain its pleiotropic biological effects.

Indexed as

Protein Biosynthesisalpha 1-AntitrypsinAnimalsBinding SitesGene Expression RegulationGenes, ReporterHep G2 CellsHumansLeukocyte ElastaseLuciferasesMiceMice, Inbred C57BLMice, KnockoutMicroarray AnalysisNAD(P)H Dehydrogenase (Quinone)Protein Bindingalpha 1-AntitrypsinLeukocyte ElastaseLuciferasesNAD(P)H Dehydrogenase (Quinone)NQO1 protein, humanRibonucleoproteinsRNA, MessengerRNA, Small InterferingSERPINA1 protein, humanA1ATmRNA translationNeutrophil elastaseNQO1RNA binding proteinSERPINA1

Identifiers

PMID27515817
PMCPMC5107118
OpenAlexW2518264493

What OpenQuestion holds

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Registered trials

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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.