Genetics of human handedness: microtubules and beyond

生物 外显子组测序 基因 遗传学 外显子组 全基因组关联研究 轴突引导 神经科学 纤毛 基因组 多效性 进化生物学 表型 轴突 单核苷酸多态性 基因型
作者
Sebastian Ocklenburg,Annakarina Mundorf,Jutta Peterburs,Silvia Paracchini
出处
期刊:Trends in Genetics [Elsevier]
标识
DOI:10.1016/j.tig.2025.01.006
摘要

HighlightsHuman handedness is a moderately heritable trait.Large-scale genome-wide association and exome sequencing studies have identified multiple genes associated with handedness and highlighted a role of tubulin genes.Axon guidance, axon growth, and forming the inner structure of motile cilia are key processes regulated by tubulin genes that may also be relevant for handedness,Tubulin genes are associated with several psychiatric disorders which may offer insights into biological pathways mediating the link between handedness, brain asymmetries, and psychiatric disorders.AbstractHandedness (i.e., the preference to use either the left or the right hand for fine motor tasks) is a widely investigated trait. Handedness heritability is consistently estimated to be 25%. After decades of research, recent large-scale genome-wide association and exome sequencing studies have identified multiple genes associated with handedness and highlighted tubulin genes. Tubulin genes play a role in several processes during brain development that may be relevant for handedness ontogenesis, including axon guidance, axon growth, and forming the inner structure of motile cilia. Moreover, tubulin genes are associated with several psychiatric disorders. This finding therefore may offer insights into biological pathways mediating the link between handedness, brain asymmetries, and psychiatric traits.

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