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Evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex
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 transcriptom...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5898914/ https://www.ncbi.nlm.nih.gov/pubmed/29561261 http://dx.doi.org/10.7554/eLife.32332 |
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author | Florio, Marta Heide, Michael Pinson, Anneline Brandl, Holger Albert, Mareike Winkler, Sylke Wimberger, Pauline Huttner, Wieland B Hiller, Michael |
author_facet | Florio, Marta Heide, Michael Pinson, Anneline Brandl, Holger Albert, Mareike Winkler, Sylke Wimberger, Pauline Huttner, Wieland B Hiller, Michael |
author_sort | Florio, Marta |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5898914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58989142018-04-16 Evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex Florio, Marta Heide, Michael Pinson, Anneline Brandl, Holger Albert, Mareike Winkler, Sylke Wimberger, Pauline Huttner, Wieland B Hiller, Michael eLife Developmental Biology 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. eLife Sciences Publications, Ltd 2018-03-21 /pmc/articles/PMC5898914/ /pubmed/29561261 http://dx.doi.org/10.7554/eLife.32332 Text en © 2018, Florio et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Florio, Marta Heide, Michael Pinson, Anneline Brandl, Holger Albert, Mareike Winkler, Sylke Wimberger, Pauline Huttner, Wieland B Hiller, Michael Evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex |
title | Evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex |
title_full | Evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex |
title_fullStr | Evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex |
title_full_unstemmed | Evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex |
title_short | Evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex |
title_sort | evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5898914/ https://www.ncbi.nlm.nih.gov/pubmed/29561261 http://dx.doi.org/10.7554/eLife.32332 |
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