Transposable element expression and sub-cellular dynamics during hPSC differentiation to endoderm, mesoderm, and ectoderm lineages

Transposable elements (TEs) are genomic elements present in multiple copies in mammalian genomes. TEs were thought to have little functional relevance but recent studies report roles in biological processes, including embryonic development. To investigate the expression dynamics of TEs during human early development, we generated long-read sequence data from human pluripotent stem cells (hPSCs) in vitro differentiated to endoderm, mesoderm, and ectoderm lineages to construct lineage-specific transcriptome assemblies and accurately place TE sequences. Our analysis reveals that specific TE superfamilies exhibit distinct expression patterns. Notably, we observed TE switching, where the same family of TE is expressed in multiple cell types, but originates from different transcripts. Interestingly, TE-containing transcripts exhibit distinct levels of transcript stability and subcellular localization. Moreover, TE-containing transcripts increasingly associate with chromatin in germ layer cells compared to hPSCs. This study suggests that TEs contribute to human embryonic development through dynamic chromatin interactions.

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Publication Details

Journal
Nature Communications
Published
2025-08-18
DOI
https://doi.org/10.1038/s41467-025-63080-3
Citations
1
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
0.81

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article

Transposable element expression and sub-cellular dynamics during hPSC differentiation to endoderm, mesoderm, and ectoderm lineages

Mobolaji T. Akinwole, Alexey Ruzov, Gang Ma, Lin Zheng et al.
1 citations
Nature Communications
RNA Research and Splicing
0.81
article

Transposable element expression and sub-cellular dynamics during hPSC differentiation to endoderm, mesoderm, and ectoderm lineages

Mobolaji T. Akinwole, Alexey Ruzov, Gang Ma, Lin Zheng, Isaac A. Babarinde, Xuemeng Zhou, Andrew P. Hutchins, Zhen Xiao, Katerina Oleynikova, Yuhao Li, Yu Qiao, Jianfei Xu, Xiuling Fu, Zhendong Liang
article en
1 citations

Abstract

Transposable elements (TEs) are genomic elements present in multiple copies in mammalian genomes. TEs were thought to have little functional relevance but recent studies report roles in biological processes, including embryonic development. To investigate the expression dynamics of TEs during human early development, we generated long-read sequence data from human pluripotent stem cells (hPSCs) in vitro differentiated to endoderm, mesoderm, and ectoderm lineages to construct lineage-specific transcriptome assemblies and accurately place TE sequences. Our analysis reveals that specific TE superfamilies exhibit distinct expression patterns. Notably, we observed TE switching, where the same family of TE is expressed in multiple cell types, but originates from different transcripts. Interestingly, TE-containing transcripts exhibit distinct levels of transcript stability and subcellular localization. Moreover, TE-containing transcripts increasingly associate with chromatin in germ layer cells compared to hPSCs. This study suggests that TEs contribute to human embryonic development through dynamic chromatin interactions.

Nature CommunicationsVol. 16(1)
Russian Academy of Sciences (RU), The University of Queensland (AU), ITMO University (RU), University of Ibadan (NG), Chinese Academy of Sciences (CN), Columbia University Irving Medical Center (US), Southern University of Science and Technology (CN), Shenzhen Institutes of Advanced Technology (CN), Southern Medical University (CN)
National Natural Science Foundation of China, Russian Science Foundation, Southern University of Science and Technology, Basic and Applied Basic Research Foundation of Guangdong Province
Openalex Percentile: Top 25%
RNA Research and Splicing
0.81
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