Integrative functional genomic analysis of human brain development and neuropsychiatric risks
Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works..
To broaden our understanding of human neurodevelopment, we profiled transcriptomic and epigenomic landscapes across brain regions and/or cell types for the entire span of prenatal and postnatal development. Integrative analysis revealed temporal, regional, sex, and cell type-specific dynamics. We observed a global transcriptomic cup-shaped pattern, characterized by a late fetal transition associated with sharply decreased regional differences and changes in cellular composition and maturation, followed by a reversal in childhood-adolescence, and accompanied by epigenomic reorganizations. Analysis of gene coexpression modules revealed relationships with epigenomic regulation and neurodevelopmental processes. Genes with genetic associations to brain-based traits and neuropsychiatric disorders (including MEF2C, SATB2, SOX5, TCF4, and TSHZ3) converged in a small number of modules and distinct cell types, revealing insights into neurodevelopment and the genomic basis of neuropsychiatric risks.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2018 |
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Erschienen: |
2018 |
Enthalten in: |
Zur Gesamtaufnahme - volume:362 |
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Enthalten in: |
Science (New York, N.Y.) - 362(2018), 6420 vom: 14. Dez. |
Sprache: |
Englisch |
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Beteiligte Personen: |
Li, Mingfeng [VerfasserIn] |
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Links: |
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Themen: |
Dataset |
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Anmerkungen: |
Date Completed 14.01.2019 Date Revised 14.02.2024 published: Print Citation Status MEDLINE |
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doi: |
10.1126/science.aat7615 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM291758177 |
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520 | |a To broaden our understanding of human neurodevelopment, we profiled transcriptomic and epigenomic landscapes across brain regions and/or cell types for the entire span of prenatal and postnatal development. Integrative analysis revealed temporal, regional, sex, and cell type-specific dynamics. We observed a global transcriptomic cup-shaped pattern, characterized by a late fetal transition associated with sharply decreased regional differences and changes in cellular composition and maturation, followed by a reversal in childhood-adolescence, and accompanied by epigenomic reorganizations. Analysis of gene coexpression modules revealed relationships with epigenomic regulation and neurodevelopmental processes. Genes with genetic associations to brain-based traits and neuropsychiatric disorders (including MEF2C, SATB2, SOX5, TCF4, and TSHZ3) converged in a small number of modules and distinct cell types, revealing insights into neurodevelopment and the genomic basis of neuropsychiatric risks | ||
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650 | 4 | |a Research Support, Non-U.S. Gov't | |
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700 | 1 | |a Imamura Kawasawa, Yuka |e verfasserin |4 aut | |
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700 | 1 | |a Gulden, Forrest O |e verfasserin |4 aut | |
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700 | 1 | |a Li, Zhen |e verfasserin |4 aut | |
700 | 1 | |a Shin, Yurae |e verfasserin |4 aut | |
700 | 1 | |a Zhu, Ying |e verfasserin |4 aut | |
700 | 1 | |a Sousa, André M M |e verfasserin |4 aut | |
700 | 1 | |a Werling, Donna M |e verfasserin |4 aut | |
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700 | 1 | |a Pletikos, Mihovil |e verfasserin |4 aut | |
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