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TBC1D3 promotes neural progenitor proliferation by suppressing the histone methyltransferase G9a
Genomic changes during human linage evolution contribute to the expansion of the cerebral cortex to allow more advanced thought processes. The hominoid-specific gene TBC1D3 displays robust capacity of promoting the generation and proliferation of neural progenitors (NPs), which are thought to contri...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7810367/ https://www.ncbi.nlm.nih.gov/pubmed/33523893 http://dx.doi.org/10.1126/sciadv.aba8053 |
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author | Hou, Qiong-Qiong Xiao, Qi Sun, Xin-Yao Ju, Xiang-Chun Luo, Zhen-Ge |
author_facet | Hou, Qiong-Qiong Xiao, Qi Sun, Xin-Yao Ju, Xiang-Chun Luo, Zhen-Ge |
author_sort | Hou, Qiong-Qiong |
collection | PubMed |
description | Genomic changes during human linage evolution contribute to the expansion of the cerebral cortex to allow more advanced thought processes. The hominoid-specific gene TBC1D3 displays robust capacity of promoting the generation and proliferation of neural progenitors (NPs), which are thought to contribute to cortical expansion. However, the underlying mechanisms remain unclear. Here, we found that TBC1D3 interacts with G9a, a euchromatic histone lysine N-methyltransferase, which mediates dimethylation of histone 3 in lysine 9 (H3K9me2), a suppressive mark for gene expression. TBC1D3 displayed an inhibitory role in G9a’s histone methyltransferase activity. Treatment with G9a inhibitor markedly increased NP proliferation and promoted human cerebral organoid expansion, mimicking the effects caused by TBC1D3 up-regulation. By contrast, blockade of TBC1D3/G9a interaction to disinhibit G9a caused up-regulation of H3K9me2, suppressed NP proliferation, and impaired organoid development. Together, this study has demonstrated a mechanism underlying the role of a hominoid-specific gene in promoting cortical expansion. |
format | Online Article Text |
id | pubmed-7810367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-78103672021-01-22 TBC1D3 promotes neural progenitor proliferation by suppressing the histone methyltransferase G9a Hou, Qiong-Qiong Xiao, Qi Sun, Xin-Yao Ju, Xiang-Chun Luo, Zhen-Ge Sci Adv Research Articles Genomic changes during human linage evolution contribute to the expansion of the cerebral cortex to allow more advanced thought processes. The hominoid-specific gene TBC1D3 displays robust capacity of promoting the generation and proliferation of neural progenitors (NPs), which are thought to contribute to cortical expansion. However, the underlying mechanisms remain unclear. Here, we found that TBC1D3 interacts with G9a, a euchromatic histone lysine N-methyltransferase, which mediates dimethylation of histone 3 in lysine 9 (H3K9me2), a suppressive mark for gene expression. TBC1D3 displayed an inhibitory role in G9a’s histone methyltransferase activity. Treatment with G9a inhibitor markedly increased NP proliferation and promoted human cerebral organoid expansion, mimicking the effects caused by TBC1D3 up-regulation. By contrast, blockade of TBC1D3/G9a interaction to disinhibit G9a caused up-regulation of H3K9me2, suppressed NP proliferation, and impaired organoid development. Together, this study has demonstrated a mechanism underlying the role of a hominoid-specific gene in promoting cortical expansion. American Association for the Advancement of Science 2021-01-15 /pmc/articles/PMC7810367/ /pubmed/33523893 http://dx.doi.org/10.1126/sciadv.aba8053 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Hou, Qiong-Qiong Xiao, Qi Sun, Xin-Yao Ju, Xiang-Chun Luo, Zhen-Ge TBC1D3 promotes neural progenitor proliferation by suppressing the histone methyltransferase G9a |
title | TBC1D3 promotes neural progenitor proliferation by suppressing the histone methyltransferase G9a |
title_full | TBC1D3 promotes neural progenitor proliferation by suppressing the histone methyltransferase G9a |
title_fullStr | TBC1D3 promotes neural progenitor proliferation by suppressing the histone methyltransferase G9a |
title_full_unstemmed | TBC1D3 promotes neural progenitor proliferation by suppressing the histone methyltransferase G9a |
title_short | TBC1D3 promotes neural progenitor proliferation by suppressing the histone methyltransferase G9a |
title_sort | tbc1d3 promotes neural progenitor proliferation by suppressing the histone methyltransferase g9a |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7810367/ https://www.ncbi.nlm.nih.gov/pubmed/33523893 http://dx.doi.org/10.1126/sciadv.aba8053 |
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