Molecules, mechanisms, and disorders of self-domestication: Keys for understanding emotional and social communication from an evolutionary perspective

Goran Šimić, Vana Vukić, Janja Kopić, Željka Krsnik, Patrick R. Hof

Research output: Contribution to journalReview articlepeer-review

15 Scopus citations

Abstract

The neural crest hypothesis states that the phenotypic features of the domestication syndrome are due to a reduced number or disruption of neural crest cells (NCCs) migration, as these cells differentiate at their final destinations and proliferate into different tissues whose activity is reduced by domestication. Comparing the phenotypic characteristics of modern and prehistoric man, it is clear that during their recent evolutionary past, humans also went through a process of self-domestication with a simultaneous prolongation of the period of socialization. This has led to the development of social abilities and skills, especially language, as well as neoteny. Disorders of neural crest cell development and migration lead to many different conditions such as Waardenburg syndrome, Hirschsprung disease, fetal alcohol syndrome, DiGeorge and Treacher-Collins syndrome, for which the mechanisms are already relatively well-known. However, for others, such as WilliamsBeuren syndrome and schizophrenia that have the characteristics of hyperdomestication, and autism spectrum disorders, and 7dupASD syndrome that have the characteristics of hypodomestication, much less is known. Thus, deciphering the biological determinants of disordered self-domestication has great potential for elucidating the normal and disturbed ontogenesis of humans, as well as for the understanding of evolution of mammals in general.

Original languageEnglish
Article number2
Pages (from-to)1-39
Number of pages39
JournalBiomolecules
Volume11
Issue number1
DOIs
StatePublished - Jan 2021

Keywords

  • Chemoattractants
  • Chemorepellents
  • Epithelial-mesenchymal transition (EMT)
  • Extracellular matrix molecules
  • Fibroblast growth factor (FGF)
  • Methyl-CpG-binding protein 2 (MeCP2)
  • Neural crest cells (NCCs)
  • Self-domestication
  • Thyroid hormones
  • Vascular endothelial growth factor (VEGF)

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