Evidence map›Paper›PMID 25753659›Full record

ArticleNucleic acids research2015

Hypoxia-induced gene expression results from selective mRNA partitioning to the endoplasmic reticulum.

Jonas J Staudacher, Isabel S Naarmann-de Vries, Stefanie J Ujvari, Bertram Klinger, Mumtaz Kasim, Edgar Benko, Antje Ostareck-Lederer, Dirk H Ostareck, Anja Bondke Persson, Stephan Lorenzen and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

28 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Chronic gestational hypoxia accelerates ovarian aging and lowers ovarian reserve in next-generation adult rats.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    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 7 institutions in 2 countries.

Jonas J StaudacherCharité - Universitätsmedizin Berlin, Institut für Vegetative Physiologie, Charitéplatz 1, D-10117 Berlin, Germany.
Isabel S Naarmann-de VriesUniversity Hospital Aachen, RWTH Aachen University, Department of Intensive and Intermediate Care, Experimental Research Unit, D-52074 Aachen, Germany.
Stefanie J UjvariCharité - Universitätsmedizin Berlin, Institut für Vegetative Physiologie, Charitéplatz 1, D-10117 Berlin, Germany.
Bertram KlingerHumboldt Universität zu Berlin, Institut für Theoretische Biologie, D-10115 Berlin, Germany Charité - Universitätsmedizin Berlin, Institut für Pathologie, D-10117 Berlin, Germany.
Mumtaz KasimCharité - Universitätsmedizin Berlin, Institut für Vegetative Physiologie, Charitéplatz 1, D-10117 Berlin, Germany.
Edgar BenkoCharité - Universitätsmedizin Berlin, Institut für Vegetative Physiologie, Charitéplatz 1, D-10117 Berlin, Germany.
Antje Ostareck-LedererUniversity Hospital Aachen, RWTH Aachen University, Department of Intensive and Intermediate Care, Experimental Research Unit, D-52074 Aachen, Germany.
Dirk H OstareckUniversity Hospital Aachen, RWTH Aachen University, Department of Intensive and Intermediate Care, Experimental Research Unit, D-52074 Aachen, Germany.
Anja Bondke PerssonCharité - Universitätsmedizin Berlin, Institut für Vegetative Physiologie, Charitéplatz 1, D-10117 Berlin, Germany.
Stephan LorenzenUniversitätsklinikum Jena, Klinik für Innere Medizin III, AG Experimentelle Nephrologie, D-07743 Jena, Germany.
Jochen C MeierMax Delbrück Center for Molecular Medicine, RNA Editing and Hyperexcitability Disorders Helmholtz Group, D-13125 Berlin, Germany TU Braunschweig, Zoological Institute, Division of Cell Physiology, D-38106 Braunschweig, Germany.
Nils BlüthgenHumboldt Universität zu Berlin, Institut für Theoretische Biologie, D-10115 Berlin, Germany Charité - Universitätsmedizin Berlin, Institut für Pathologie, D-10117 Berlin, Germany.
Pontus B PerssonCharité - Universitätsmedizin Berlin, Institut für Vegetative Physiologie, Charitéplatz 1, D-10117 Berlin, Germany.
Alexandra Henrion-CaudeHôpital Necker-Enfants Malades, Université Paris Descartes, Institut National de la Santé et de la Recherche Médicale (INSERM) UMR1163 and Imagine Foundation, 75015 Paris, France.
Ralf MrowkaUniversitätsklinikum Jena, Klinik für Innere Medizin III, AG Experimentelle Nephrologie, D-07743 Jena, Germany.
Michael FählingCharité - Universitätsmedizin Berlin, Institut für Vegetative Physiologie, Charitéplatz 1, D-10117 Berlin, Germany michael.faehling@charite.de.
Charité - Universitätsmedizin Berlin · DEJena University Hospital · DEUniversitätsklinikum Aachen · DEHôpital Necker-Enfants Malades · FRHumboldt-Universität zu Berlin · DERWTH Aachen University · DETechnische Universität Braunschweig · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein synthesis is a primary energy-consuming process in the cell. Therefore, under hypoxic conditions, rapid inhibition of global mRNA translation represents a major protective strategy to maintain energy metabolism. How some mRNAs, especially those that encode crucial survival factors, continue to be efficiently translated in hypoxia is not completely understood. By comparing specific transcript levels in ribonucleoprotein complexes, cytoplasmic polysomes and endoplasmic reticulum (ER)-bound ribosomes, we show that the synthesis of proteins encoded by hypoxia marker genes is favoured at the ER in hypoxia. Gene expression profiling revealed that transcripts particularly increased by the HIF-1 transcription factor network show hypoxia-induced enrichment at the ER. We found that mRNAs favourably translated at the ER have higher conservation scores for both the 5'- and 3'-untranslated regions (UTRs) and contain less upstream initiation codons (uAUGs), indicating the significance of these sequence elements for sustained mRNA translation under hypoxic conditions. Furthermore, we found enrichment of specific cis-elements in mRNA 5'- as well as 3'-UTRs that mediate transcript localization to the ER in hypoxia. We conclude that transcriptome partitioning between the cytoplasm and the ER permits selective mRNA translation under conditions of energy shortage.

Indexed as

Cell HypoxiaCell LineCodon, InitiatorCytoplasmEndoplasmic ReticulumGene ExpressionGenetic MarkersHumansHypoxia-Inducible Factor 1, alpha SubunitProcollagen-Proline DioxygenaseProtein BiosynthesisProtein Disulfide-IsomerasesRibosomesRNA, MessengerTranscriptomeCodon, InitiatorGenetic MarkersHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitP4HA1 protein, humanP4HB protein, humanProcollagen-Proline DioxygenaseProtein Disulfide-IsomerasesRNA, Messenger

Identifiers

PMID25753659
PMCPMC4381074
OpenAlexW1986500735

What OpenQuestion holds

Textmetadata
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.