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Dosage analysis of the 7q11.23 Williams region identifies BAZ1B as a major human gene patterning the modern human face and underlying self-domestication.


ABSTRACT: We undertook a functional dissection of chromatin remodeler BAZ1B in neural crest (NC) stem cells (NCSCs) from a uniquely informative cohort of typical and atypical patients harboring 7q11.23 copy number variants. Our results reveal a key contribution of BAZ1B to NCSC in vitro induction and migration, coupled with a crucial involvement in NC-specific transcriptional circuits and distal regulation. By intersecting our experimental data with new paleogenetic analyses comparing modern and archaic humans, we found a modern-specific enrichment for regulatory changes both in BAZ1B and its experimentally defined downstream targets, thereby providing the first empirical validation of the human self-domestication hypothesis and positioning BAZ1B as a master regulator of the modern human face. In so doing, we provide experimental evidence that the craniofacial and cognitive/behavioral phenotypes caused by alterations of the Williams-Beuren syndrome critical region can serve as a powerful entry point into the evolution of the modern human face and prosociality.

SUBMITTER: Zanella M 

PROVIDER: S-EPMC6892627 | biostudies-literature | 2019 Dec

REPOSITORIES: biostudies-literature

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Dosage analysis of the 7q11.23 Williams region identifies <i>BAZ1B</i> as a major human gene patterning the modern human face and underlying self-domestication.

Zanella Matteo M   Vitriolo Alessandro A   Andirko Alejandro A   Martins Pedro Tiago PT   Sturm Stefanie S   O'Rourke Thomas T   Laugsch Magdalena M   Malerba Natascia N   Skaros Adrianos A   Trattaro Sebastiano S   Germain Pierre-Luc PL   Mihailovic Marija M   Merla Giuseppe G   Rada-Iglesias Alvaro A   Boeckx Cedric C   Testa Giuseppe G  

Science advances 20191204 12


We undertook a functional dissection of chromatin remodeler BAZ1B in neural crest (NC) stem cells (NCSCs) from a uniquely informative cohort of typical and atypical patients harboring 7q11.23 copy number variants. Our results reveal a key contribution of BAZ1B to NCSC in vitro induction and migration, coupled with a crucial involvement in NC-specific transcriptional circuits and distal regulation. By intersecting our experimental data with new paleogenetic analyses comparing modern and archaic h  ...[more]

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