Evidence map›Paper›PMID 34471131›Full record

ArticleNature communications2021

Loss of SNORA73 reprograms cellular metabolism and protects against steatohepatitis.

Arthur C Sletten, Jessica W Davidson, Busra Yagabasan, Samantha Moores, Michaela Schwaiger-Haber, Hideji Fujiwara, Sarah Gale, Xuntian Jiang, Rohini Sidhu, Susan J Gelman and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. LncRNA SNHG3: a potential biomarker for human diseases.Frontiers in cell and developmental biology · 2026
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. LncRNAeLife · 2024
    Article
  15. Article
  16. Review
  17. SnoRNAs: Exploring Their Implication in Human Diseases.International journal of molecular sciences · 2024
    Review
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Arthur C SlettenDepartment of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Jessica W DavidsonJoslin Diabetes Center, Harvard Medical School, Boston, MA, USA.
Busra YagabasanJoslin Diabetes Center, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0003-4351-6165
Samantha MooresJoslin Diabetes Center, Harvard Medical School, Boston, MA, USA.
Michaela Schwaiger-HaberDepartment of Chemistry, Washington University in St. Louis, St. Louis, MO, USA.ORCID http://orcid.org/0000-0002-2715-753X
Hideji FujiwaraDepartment of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Sarah GaleDepartment of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Xuntian JiangDepartment of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Rohini SidhuDepartment of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Susan J GelmanDepartment of Chemistry, Washington University in St. Louis, St. Louis, MO, USA.
Shuang ZhaoDepartment of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Gary J PattiDepartment of Chemistry, Washington University in St. Louis, St. Louis, MO, USA.ORCID http://orcid.org/0000-0002-3748-6193
Daniel S OryDepartment of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Jean E SchafferJoslin Diabetes Center, Harvard Medical School, Boston, MA, USA. jean.schaffer@joslin.harvard.edu.ORCID http://orcid.org/0000-0002-4954-6659
Washington University in St. Louis · USJoslin Diabetes Center · US

Funding

NATIONAL RESEARCH SERVICE AWARD-MEDICAL SCIENTISTT32GM007200 · NIGMS · WASHINGTON UNIVERSITY · PI YOKOYAMA, WAYNE M. · 1985 to 2024
$59.8M
SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI JEAN E. SCHAFFER · 1986 to 2026
$50.5M
Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Brian N Finck · 1999 to 2026
$30.2M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI FUMIHIKO URANO · 2013 to 2026
$27.1M
CARDIOVASCULAR SYSTEM--FUNCTION/REGULATION/PHARMACOLOGYT32HL007275 · NHLBI · WASHINGTON UNIVERSITY · PI NERBONNE, JEANNE M. · 1985 to 2013
$6.0M
Developing Metabolomic Technologies to Advance Environmental Exposure AnalysisR35ES028365 · NIEHS · WASHINGTON UNIVERSITY · PI PATTI, GARY J · 2017 to 2024
$5.9M
CELLULAR MECHANISMS THAT PROMOTE OR PREVENT LIPOTOXICITYR01DK064989 · NIDDK · WASHINGTON UNIVERSITY · PI SCHAFFER, JEAN E. · 2003 to 2021
$5.8M
Tissue Responses to Metabolic StressR01DK108357 · NIDDK · WASHINGTON UNIVERSITY · PI SCHAFFER, JEAN E. · 2016 to 2019
$2.0M
Training in Integrative and Systems Biology of Cardiovascular DiseaseT32HL134635 · NHLBI · WASHINGTON UNIVERSITY · PI NERBONNE, JEANNE M. · 2017 to 2021
$1.8M
Regulation of metabolic stress by the Snhg3 locus.F30DK120141 · NIDDK · WASHINGTON UNIVERSITY · PI SLETTEN, ARTHUR CURTIS · 2018 to 2021
$155k
NHLBI NIH HHS T32 HL007275NHLBI NIH HHS T32 HL134635NIDDK NIH HHS F30 DK120141NIDDK NIH HHS P30 DK020579NIDDK NIH HHS P30 DK036836NIDDK NIH HHS P30 DK056341NIDDK NIH HHS R01 DK064989NIDDK NIH HHS R01 DK108357NIEHS NIH HHS R35 ES028365NIGMS NIH HHS T32 GM007200U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) T32 GM07200
6 · The paper itself

Abstract

Dyslipidemia and resulting lipotoxicity are pathologic signatures of metabolic syndrome and type 2 diabetes. Excess lipid causes cell dysfunction and induces cell death through pleiotropic mechanisms that link to oxidative stress. However, pathways that regulate the response to metabolic stress are not well understood. Herein, we show that disruption of the box H/ACA SNORA73 small nucleolar RNAs encoded within the small nucleolar RNA hosting gene 3 (Snhg3) causes resistance to lipid-induced cell death and general oxidative stress in cultured cells. This protection from metabolic stress is associated with broad reprogramming of oxidative metabolism that is dependent on the mammalian target of rapamycin signaling axis. Furthermore, we show that knockdown of SNORA73 in vivo protects against hepatic steatosis and lipid-induced oxidative stress and inflammation. Our findings demonstrate a role for SNORA73 in the regulation of metabolism and lipotoxicity.

Indexed as

AnimalsCell DeathCHO CellsCricetulusDiabetes Mellitus, Type 2Fatty LiverHomeostasisInflammationLipid MetabolismLipidsMaleMetabolic SyndromeMiceMice, Inbred C57BLOxidative StressProtective AgentsLipidsProtective AgentsRNA, Long NoncodingRNA, Small Nucleolar

Identifiers

PMID34471131
PMCPMC8410784
OpenAlexW3196514628

What OpenQuestion holds

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LicenceCC BY
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.