Evidence map›Paper›PMID 26572639›Full record

ArticleMolecular neurobiology2016

Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy Adults.

Sebastian Ocklenburg, Larissa Arning, Wanda M Gerding, Jan G Hengstler, Jörg T Epplen, Onur Güntürkün, Christian Beste, Denis A Akkad

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In one paragraph

Article in Molecular neurobiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

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

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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

8 authors at 4 institutions in 1 country.

Sebastian OcklenburgInstitute of Cognitive Neuroscience, Biopsychology, Department of Psychology, Ruhr-University, 44780, Bochum, Germany. sebastian.ocklenburg@rub.de.
Larissa ArningDepartment of Human Genetics, Ruhr-University, 44780, Bochum, Germany.
Wanda M GerdingDepartment of Human Genetics, Ruhr-University, 44780, Bochum, Germany.
Jan G HengstlerLeibniz Research Centre for Working Environment and Human Factors (IfADo), 44139, Dortmund, Germany.
Jörg T EpplenDepartment of Human Genetics, Ruhr-University, 44780, Bochum, Germany.
Onur GüntürkünInstitute of Cognitive Neuroscience, Biopsychology, Department of Psychology, Ruhr-University, 44780, Bochum, Germany.
Christian BesteCognitive Neurophysiology, Department of Child and Adolescent Psychiatry, Faculty of Medicine of the TU Dresden, 01309, Dresden, Germany.
Denis A AkkadDepartment of Human Genetics, Ruhr-University, 44780, Bochum, Germany.
Ruhr University Bochum · DETU Dortmund University · DETU Dresden · DEWitten/Herdecke University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Handedness is a multifactorial trait, and genes contributing to the differentiation of the left-right axis during embryogenesis have been identified as a major gene group associated with this trait. The methyltransferase SETDB2 (SET domain, bifurcated 2) has been shown to regulate structural left-right asymmetry in the vertebrate central nervous system by suppressing fgf8 expression. Here, we investigated the relation of genetic variation in SETDB2-and its paralogue SETDB1-with different handedness phenotypes in 950 healthy adult participants. We identified a haplotype on SETDB2 for which homozygous individuals showed a significantly lower lateralization quotient for handedness than the rest of the cohort after correction for multiple comparisons. Moreover, direction of handedness was significantly associated with genetic variation in this haplotype. This effect was mainly, but not exclusively, driven by the sequence variation rs4942830, as individuals homozygous for the A allele of this single nucleotide polymorphism had a significantly lower lateralization quotient than individuals with at least one T allele. These findings further confirm a role of genetic pathways relevant for structural left-right axis differentiation for functional lateralization. Moreover, as the protein encoded by SETDB2 regulates gene expression epigenetically by histone H3 methylation, our findings highlight the importance of investigating the role of epigenetic modulations of gene expression in relation to handedness.

Indexed as

AdultAnalysis of VarianceBody PatterningFemaleFunctional LateralityHaplotypesHistone-Lysine N-MethyltransferaseHumansMalePhenotypePolymorphism, Single NucleotideHistone-Lysine N-MethyltransferaseSETDB2 protein, humanCerebral asymmetriesDirection of lateralizationGenetic association studyLateralityLateralizationOntogenesisSNP

Identifiers

PMID26572639
OpenAlexW2200379746

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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.