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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...

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Autores principales: Hou, Qiong-Qiong, Xiao, Qi, Sun, Xin-Yao, Ju, Xiang-Chun, Luo, Zhen-Ge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
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.
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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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