Evidence map›Paper›PMID 16044173›Full record

ArticleMolecular psychiatry2005

Alternative transcripts and evidence of imprinting of GNAL on 18p11.2.

J P Corradi, V Ravyn, A K Robbins, K W Hagan, M F Peters, R Bostwick, R J Buono, W H Berrettini, S T Furlong

Abstract read
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In one paragraph

Article in Molecular psychiatry, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-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

19 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Identification of genomic locus responsible for experimentally induced testicular teratoma 1 (ett1) on mouse Chr 18.Mammalian genome : official journal of the International Mammalian Genome Society · 2014
    Article
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  8. Article
  9. Article
  10. Association between polymorphisms in the metallophosphoesterase (MPPE1) gene and bipolar disorder.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2010
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Monosomy 18p.Orphanet journal of rare diseases · 2008
    Review
  17. Epigenetics in mood disorders.Environmental health and preventive medicine · 2008
    Article
  18. Article
  19. 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

9 authors at 4 institutions in 2 countries.

J P CorradiDepartment of Target Biology, AstraZeneca Pharmaceuticals, Wilmington, DE, USA.
V Ravyn
A K Robbins
K W Hagan
M F Peters
R Bostwick
R J Buono
W H Berrettini
S T Furlong
AstraZeneca (United States) · USAstraZeneca (United Kingdom) · GBTarget (United States) · USUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic studies implicating the region of human chromosome 18p11.2 in susceptibility to bipolar disorder and schizophrenia have observed parent-of-origin effects that may be explained by genomic imprinting. We have identified a transcriptional variant of the GNAL gene in this region, employing an alternative first exon that is 5' to the originally identified start site. This alternative GNAL transcript encodes a longer functional variant of the stimulatory G-protein alpha subunit, Golf. The isoforms of Golf display different expression patterns in the CNS and functionally couple to the dopamine D1 receptor when heterologously expressed in Sf9 cells. In addition, there are CpG islands in the vicinity of both first exons that are differentially methylated, a hallmark of genomic imprinting. These results suggest that GNAL, and possibly other genes in the region, is subject to epigenetic regulation and strengthen the case for a susceptibility gene in this region.

Indexed as

Alternative SplicingGenomic ImprintingAmino Acid SequenceAnimalsBase SequenceBipolar DisorderCell LineCentral Nervous SystemChromosomes, Human, Pair 18CpG IslandsDNA, ComplementaryDNA MethylationEpigenesis, GeneticExonsFemaleGTP-Binding Protein alpha SubunitsDNA, ComplementaryGTP-Binding Protein alpha Subunitsolfactory G protein subunit alpha olfRecombinant Proteins

Identifiers

PMID16044173
OpenAlexW2065686978

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.