Evidence map›Paper›PMID 17553827›Full record

ArticleNucleic acids research2007

The selenoproteome exhibits widely varying, tissue-specific dependence on selenoprotein P for selenium supply.

Peter R Hoffmann, Simone C Höge, Ping-An Li, Fukun W Hoffmann, Ann C Hashimoto, Marla J Berry

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

62 citing papers in PubMed, 178 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. The role of selenoproteins in neutrophils during inflammation.Archives of biochemistry and biophysics · 2022
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Selenium at theFrontiers in neuroscience · 2021
    Review

2 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Peter R HoffmannDepartment of Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI 96813, USA. peterh@pbrc.hawaii.edu
Simone C Höge
Ping-An Li
Fukun W Hoffmann
Ann C Hashimoto
Marla J Berry
University of Hawaiʻi at Mānoa · USUniversity of Hawaii System · US

Funding

MECHANISM OF SELENOPROTEIN SYNTHESIS IN EUKARYOTESR01DK047320 · NIDDK · UNIVERSITY OF HAWAII AT MANOA · PI BERRY, MARLA J · 1994 to 2020
$5.8M
SELENOPROTEIN P FUNCTION AND REGULATION OF EXPRESSIONR01NS040302 · NINDS · UNIVERSITY OF HAWAII AT MANOA · PI BERRY, MARLA J · 2000 to 2007
$2.8M
ALTERNATIVE MECHANISMS OF UGA CODON RECOGNITIONR01DK052963 · NIDDK · UNIVERSITY OF HAWAII AT MANOA · PI BERRY, MARLA J · 1997 to 2005
$1.4M
MECHANISM OF SELENOPROTEIN SYNTHESISR56DK047320 · NIDDK · UNIVERSITY OF HAWAII AT MANOA · PI BERRY, MARLA J · 2009 to 2009
$368k
NIDDK NIH HHS DK47320NIDDK NIH HHS DK52963NIDDK NIH HHS R01 DK047320NIDDK NIH HHS R01 DK052963NIDDK NIH HHS R56 DK047320NINDS NIH HHS R01 NS040302NINDS NIH HHS R01 NS40302
6 · The paper itself

Abstract

Selenoprotein P (Sel P) is a selenium-rich glycoprotein believed to play a key role in selenium (Se) transport throughout the body. Development of a Sel P knockout mouse model has supported this notion and initial studies have indicated that selenium supply to various tissues is differentially affected by genetic deletion of Sel P. Se in the form of the amino acid, selenocysteine, is incorporated into selenoproteins at UGA codons. Thus, Se availability affects not only selenoprotein levels, but also the turnover of selenoprotein mRNAs via the nonsense-mediated decay pathway. We investigated how genetic deletion of Sel P in mice affected levels of the mRNAs encoding all known members of the murine selenoprotein family, as well as three non-selenoprotein factors involved in their synthesis, selenophosphate synthetase 1 (SPS1), SECIS-binding protein 2 (SBP2) and SECp43. Our findings present a comprehensive description of selenoprotein mRNA expression in the following murine tissues: brain, heart, intestine, kidney, liver, lung, spleen and testes. We also describe how abundance of selenoproteins and selenoprotein-synthesis factors are affected by genetic deletion of Sel P in some of these tissues, providing insight into how the presence of this selenoprotein influences selenoprotein mRNA levels, and thus, the selenoproteome.

Indexed as

AnimalsBrainLungMaleMiceMice, Inbred C57BLMice, KnockoutMyocardiumProteomeRNA, MessengerSeleniumSelenoprotein PSelenoproteinsTestisTissue DistributionProteomeRNA, MessengerSeleniumSelenoprotein PSelenoproteins

Identifiers

PMID17553827
PMCPMC1919489
OpenAlexW2161771658

What OpenQuestion holds

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LicenceCC BY-NC
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.