Evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex

Author:

Florio Marta1,Heide Michael1,Pinson Anneline1,Brandl Holger1ORCID,Albert Mareike1,Winkler Sylke1,Wimberger Pauline2,Huttner Wieland B1ORCID,Hiller Michael13

Affiliation:

1. Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany

2. Klinik und Poliklinik für Frauenheilkunde und Geburtshilfe, Universitätsklinikum Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany

3. Max Planck Institute for the Physics of Complex Systems, Dresden, Germany

Abstract

Understanding the molecular basis that underlies the expansion of the neocortex during primate, and notably human, evolution requires the identification of genes that are particularly active in the neural stem and progenitor cells of the developing neocortex. Here, we have used existing transcriptome datasets to carry out a comprehensive screen for protein-coding genes preferentially expressed in progenitors of fetal human neocortex. We show that 15 human-specific genes exhibit such expression, and many of them evolved distinct neural progenitor cell-type expression profiles and levels compared to their ancestral paralogs. Functional studies on one such gene, NOTCH2NL, demonstrate its ability to promote basal progenitor proliferation in mice. An additional 35 human genes with progenitor-enriched expression are shown to have orthologs only in primates. Our study provides a resource of genes that are promising candidates to exert specific, and novel, roles in neocortical development during primate, and notably human, evolution.

Funder

Max-Planck-Gesellschaft

Deutsche Forschungsgemeinschaft

European Research Council

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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