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

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Florio,  Marta
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Heide,  Michael
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Pinson,  Anneline
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Brandl,  Holger
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Albert,  Mareike
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Winkler,  Sylke
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Huttner,  Wieland B.
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

/persons/resource/persons184581

Hiller,  Michael
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Citation

Florio, M., Heide, M., Pinson, A., Brandl, H., Albert, M., Winkler, S., et al. (2018). Evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex. eLife, 7: e32332. doi:10.7554/eLife.32332.


Cite as: https://hdl.handle.net/21.11116/0000-0003-F5E5-6
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 fifteen 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.