Evidence map›Paper›PMID 16503985›Full record

ArticleBMC neuroscience2006

Genomic regulation of natural variation in cortical and noncortical brain volume.

Jackson Beatty, Rick E Laughlin

Open access · goldAbstract read
In one paragraph

Article in BMC neuroscience, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Quantitative Trait Loci and a Novel Genetic Candidate for Fear Learning.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  5. Article
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  8. Teaching neuroinformatics with an emphasis on quantitative locus analysis.Journal of undergraduate neuroscience education : JUNE : a publication of FUN, Faculty for Undergraduate Neuroscience · 2012
    Article
  9. Expression of the homeobox genes OTX2 and OTX1 in the early developing human brain.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2010
    Article
  10. Article
  11. Article
  12. Article
  13. Article
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  15. The Neuroterrain 3D Mouse Brain Atlas.Frontiers in neuroinformatics · 2008
    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

2 authors at 1 institution in 1 country.

Jackson BeattyDepartment of Psychology, University of California, Los Angeles, California, USA. beatty@ucla.edu
Rick E Laughlin
University of California, Los Angeles · US

Funding

SCALABLE INSTRUCTION IN NEUROINFORMATICS AT UCLAK07MH001953 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BEATTY, JACKSON T · 2000 to 2004
$316k
NIDCD NIH HHS DC/8424559NIMH NIH HHS 1K07MH01953NIMH NIH HHS K07 MH001953
6 · The paper itself

Abstract

backgroundThe relative growth of the neocortex parallels the emergence of complex cognitive functions across species. To determine the regions of the mammalian genome responsible for natural variations in cortical volume, we conducted a complex trait analysis using 34 strains of recombinant inbred (Rl) strains of mice (BXD), as well as their two parental strains (C57BL/6J and DBA/2J). We measured both neocortical volume and total brain volume in 155 coronally sectioned mouse brains that were Nissl stained and embedded in celloidin. After correction for shrinkage, the measured cortical and noncortical brain volumes were entered into a multiple regression analysis, which removed the effects of body size and age from the measurements. Marker regression and interval mapping were computed using WebQTL.

resultsAn ANOVA revealed that more than half of the variance of these regressed phenotypes is genetically determined. We then identified the regions of the genome regulating this heritability. We located genomic regions in which a linkage disequilibrium was present using WebQTL as both a mapping engine and genomic database. For neocortex, we found a genome-wide significant quantitative trait locus (QTL) on chromosome 11 (marker D11Mit19), as well as a suggestive QTL on chromosome 16 (marker D16Mit100). In contrast, for noncortex the effect of chromosome 11 was markedly reduced, and a significant QTL appeared on chromosome 19 (D19Mit22).

conclusionThis classic pattern of double dissociation argues strongly for different genetic factors regulating relative cortical size, as opposed to brain volume more generally. It is likely, however, that the effects of proximal chromosome 11 extend beyond the neocortex strictly defined. An analysis of single nucleotide polymorphisms in these regions indicated that ciliary neurotrophic factor (Cntf) is quite possibly the gene underlying the noncortical QTL. Evidence for a candidate gene modulating neocortical volume was much weaker, but Otx1 deserves further consideration.

Indexed as

Quantitative Trait LociAnimalsBody SizeBrainCerebral CortexChromosome MappingCrosses, GeneticFemaleGenetic VariationLinkage DisequilibriumMaleMiceMice, Inbred C57BLMice, Inbred DBAMultifactorial InheritanceOrgan Size

Identifiers

PMID16503985
PMCPMC1402304
OpenAlexW1491417747

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.