Evolutionary Gain of Dbx1 Expression Drives Subplate Identity in the Cerebral Cortex
Author(s) -
Yoko Arai,
Andrzej Cwetsch,
Eva Coppola,
Sara Cipriani,
Hidenori Nishihara,
Hiroaki Kanki,
Yoann Saillour,
Betty Freret-Hodara,
Annie Dutriaux,
Norihiro Okada,
Hideyuki Okano,
Colette Dehay,
Jeannette Nardelli,
Pierre Gressèns,
Tomomi Shimogori,
Giuseppe D’Onofrio,
Alessandra Pierani
Publication year - 2019
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2019.09.007
Subject(s) - subplate , biology , neuroscience , cerebral cortex , ganglionic eminence , ectopic expression , marmoset , cortex (anatomy) , embryonic stem cell , progenitor , progenitor cell , primate , interneuron , microbiology and biotechnology , gene , stem cell , central nervous system , cerebrum , genetics , inhibitory postsynaptic potential , paleontology
Changes in transcriptional regulation through cis-regulatory elements are thought to drive brain evolution. However, how this impacts the identity of primate cortical neurons is still unresolved. Here, we show that primate-specific cis-regulatory sequences upstream of the Dbx1 gene promote human-like expression in the mouse embryonic cerebral cortex, and this imparts cell identity. Indeed, while Dbx1 is expressed in highly restricted cortical progenitors in the mouse ventral pallium, it is maintained in neurons in primates. Phenocopy of the primate-like Dbx1 expression in mouse cortical progenitors induces ectopic Cajal-Retzius and subplate (SP) neurons, which are transient populations playing crucial roles in cortical development. A conditional expression solely in neurons uncouples mitotic and postmitotic activities of Dbx1 and exclusively promotes a SP-like fate. Our results highlight how transcriptional changes of a single fate determinant in postmitotic cells may contribute to the expansion of neuronal diversity during cortical evolution.
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