Evidence map›Paper›PMID 27059230›Full record

ArticleJournal of molecular neuroscience : MN2016

LINC00507 Is Specifically Expressed in the Primate Cortex and Has Age-Dependent Expression Patterns.

James D Mills, Melanie Ward, Bei Jun Chen, Anand M Iyer, Eleonora Aronica, Michael Janitz

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In one paragraph

Article in Journal of molecular neuroscience : MN, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Advances in transcriptome analysis of human brain aging.Experimental & molecular medicine · 2020
    Review
  9. Article
  10. Article
  11. Sleep Deprivation and the Epigenome.Frontiers in neural circuits · 2018
    Review
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 3 institutions in 2 countries.

James D MillsSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, NSW, Sydney, 2052, Australia.
Melanie WardSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, NSW, Sydney, 2052, Australia.
Bei Jun ChenSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, NSW, Sydney, 2052, Australia.
Anand M IyerDepartment of (Neuro) Pathology, Academic Medical Center and Swammerdam Institute for Life Sciences, Center for Neuorscience, University of Amsterdam, Amsterdam, The Netherlands.
Eleonora AronicaDepartment of (Neuro) Pathology, Academic Medical Center and Swammerdam Institute for Life Sciences, Center for Neuorscience, University of Amsterdam, Amsterdam, The Netherlands.
Michael JanitzSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, NSW, Sydney, 2052, Australia. m.janitz@unsw.edu.au.
UNSW Sydney · AUAcademic Medical Center · NLUniversity of Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the past decade, there has been an increase in the appreciation of the role of non-coding RNA in the development of organism phenotype. It is possible to divide the non-coding elements of the transcriptome into three categories: short non-coding RNAs, circular RNAs and long non-coding RNAs. Long non-coding RNAs are those transcripts that are greater than 200 nts in length and lack any significant open reading frames that produce proteins greater then 100 amino acids. Long intervening non-coding RNAs (lincRNAs) are a subclass of long non-coding RNAs. In contrast to protein coding RNAs, lincRNAs are expressed in a more tissue- and species-specific manner. In particular, many lincRNAs are only conserved amongst higher primates. This coupled with the propensity of many lincRNAs to be expressed in the brain, suggests that they are in fact one of the major drivers of organism complexity. We analysed 39 lincRNAs that are expressed in the frontal cortex and identified LINC00507 as being expressed in a cortex-specific manner in non-human primates and humans. The expression patterns of LINC00507 appear to be age-dependent, suggesting it may be involved in brain development of higher primates. Moreover, the analysis of LINC00507 potential to bind ribosomes revealed that this previously identified non-coding transcript may harbour a micropeptide.

Indexed as

AnimalsCerebral CortexConserved SequenceGene Expression Regulation, DevelopmentalOrgan SpecificityPrimatesRNA, Long NoncodingRNA, Long NoncodingBrainCerebral cortexLINC00507lincRNAsMicropeptideNon-coding RNARNA-Seq

Identifiers

PMID27059230
OpenAlexW2326521017

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.