Evidence map›Paper›PMID 20685873›Full record

ArticleEndocrinology2010

Nocturnin suppresses igf1 expression in bone by targeting the 3' untranslated region of igf1 mRNA.

Masanobu Kawai, Anne M Delany, Carla B Green, Martin L Adamo, Clifford J Rosen

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  15. Review
  16. Minireview: mechanisms of growth hormone-mediated gene regulation.Molecular endocrinology (Baltimore, Md.) · 2014
    Review
  17. Article
  18. Posttranscriptional regulation of insulin family ligands and receptors.International journal of molecular sciences · 2013
    Review
  19. 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

5 authors at 4 institutions in 1 country.

Masanobu KawaiCenter for Translational Research, Maine Medical Center Research Institute, 81 Research Drive, Scarborough, Maine 04074-7205, USA.
Anne M Delany
Carla B Green
Martin L Adamo
Clifford J Rosen
Maine Medical Center Research Institute · USThe University of Texas Health Science Center at San Antonio · USThe University of Texas Southwestern Medical Center · USUConn Health · US

Funding

Genetics of IGF1 and Bone Density: The Role of NocturninR01AR045433 · NIAMS · MAINEHEALTH · PI ROSEN, CLIFFORD JAMES · 1998 to 2012
$6.8M
Function and Regulation of Osteonectin in BoneR01AR044877 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI DELANY, ANNE M · 2003 to 2013
$2.6M
A Chromosome 10 QTL Associated with IGF-1 and Bone MassR01AR053853 · NIAMS · MAINEHEALTH · PI ROSEN, CLIFFORD JAMES · 2007 to 2010
$2.2M
Circadian post-transcriptional regulatory mechanismsR01GM076626 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI GREEN, CARLA B. · 2006 to 2009
$1.3M
NIAMS NIH HHS AR45433NIAMS NIH HHS AR 53853NIAMS NIH HHS R01 AR044877NIAMS NIH HHS R01 AR045433NIAMS NIH HHS R01 AR053853NIGMS NIH HHS GM076626NIGMS NIH HHS R01 GM076626
6 · The paper itself

Abstract

IGF-I is an anabolic factor that mediates GH and PTH actions in bone. Expression of skeletal Igf1 differs for inbred strains of mice, and Igf expression levels correlate directly with bone mass. Previously we reported that peroxisome proliferator-activated receptor-γ2 activation in bone marrow suppressed Igf1 expression and that peroxisome proliferator-activated receptor-γ2 activation-induced Nocturnin (Noc) expression, a circadian gene with peak expression at light offset, which functions as a deadenylase. In 24-h studies we found that Igf1 mRNA exhibited a circadian rhythm in femur with the lowest Igf1 transcript levels at night when Noc transcripts were highest. Immunoprecipitation/RT-PCR analysis revealed a physical interaction between Noc protein and Igf1 transcripts. To clarify which portions of the Igf1 3' untranslated region (UTR) were necessary for regulation by Noc, we generated luciferase constructs containing various lengths of the Igf1 3'UTR. Noc did not affect the 170-bp short-form 3'UTR, but suppressed luciferase activity in constructs bearing the longer-form 3'UTR, which contains a number of potential regulatory motifs involved in mRNA degradation. C57BL/6J mice have low skeletal Igf1 mRNA compared with C3H/HeJ mice, and the Igf1 3' UTR is polymorphic between these strains. Interestingly, the activity of luciferase constructs bearing the long-form 3'UTR from C57BL/6J mice were repressed by Noc overexpression, whereas those bearing the corresponding region from C3H/HeJ were not. In summary, Noc interacts with Igf1 in a strain- and tissue-specific manner and reduces Igf1 expression by targeting the longer form of the Igf1 3'UTR. Posttranscriptional regulation of Igf1 may be critically important during skeletal acquisition and maintenance.

Indexed as

3' Untranslated RegionsAnimalsAnimals, NewbornBone and BonesCells, CulturedCircadian RhythmDown-RegulationFemaleGene TargetingInsulin-Like Growth Factor IMiceMice, Inbred C3HMice, Inbred C57BLMice, KnockoutNuclear ProteinsOrgan Specificity3' Untranslated RegionsInsulin-Like Growth Factor InocturninNuclear ProteinsRNA, MessengerTranscription Factors

Identifiers

PMID20685873
PMCPMC2946149
OpenAlexW2143335836

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.