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T-REX17 is a transiently expressed non-coding RNA essential for human endoderm formation
Long non-coding RNAs (lncRNAs) have emerged as fundamental regulators in various biological processes, including embryonic development and cellular differentiation. Despite much progress over the past decade, the genome-wide annotation of lncRNAs remains incomplete and many known non-coding loci are...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889090/ https://www.ncbi.nlm.nih.gov/pubmed/36719724 http://dx.doi.org/10.7554/eLife.83077 |
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author | Landshammer, Alexandro Bolondi, Adriano Kretzmer, Helene Much, Christian Buschow, René Rose, Alina Wu, Hua-Jun Mackowiak, Sebastian D Braendl, Bjoern Giesselmann, Pay Tornisiello, Rosaria Parsi, Krishna Mohan Huey, Jack Mielke, Thorsten Meierhofer, David Maehr, René Hnisz, Denes Michor, Franziska Rinn, John L Meissner, Alexander |
author_facet | Landshammer, Alexandro Bolondi, Adriano Kretzmer, Helene Much, Christian Buschow, René Rose, Alina Wu, Hua-Jun Mackowiak, Sebastian D Braendl, Bjoern Giesselmann, Pay Tornisiello, Rosaria Parsi, Krishna Mohan Huey, Jack Mielke, Thorsten Meierhofer, David Maehr, René Hnisz, Denes Michor, Franziska Rinn, John L Meissner, Alexander |
author_sort | Landshammer, Alexandro |
collection | PubMed |
description | Long non-coding RNAs (lncRNAs) have emerged as fundamental regulators in various biological processes, including embryonic development and cellular differentiation. Despite much progress over the past decade, the genome-wide annotation of lncRNAs remains incomplete and many known non-coding loci are still poorly characterized. Here, we report the discovery of a previously unannotated lncRNA that is transcribed 230 kb upstream of the SOX17 gene and located within the same topologically associating domain. We termed it T-REX17 (Transcript Regulating Endoderm and activated by soX17) and show that it is induced following SOX17 activation but its expression is more tightly restricted to early definitive endoderm. Loss of T-REX17 affects crucial functions independent of SOX17 and leads to an aberrant endodermal transcriptome, signaling pathway deregulation and epithelial to mesenchymal transition defects. Consequently, cells lacking the lncRNA cannot further differentiate into more mature endodermal cell types. Taken together, our study identified and characterized T-REX17 as a transiently expressed and essential non-coding regulator in early human endoderm differentiation. |
format | Online Article Text |
id | pubmed-9889090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-98890902023-02-01 T-REX17 is a transiently expressed non-coding RNA essential for human endoderm formation Landshammer, Alexandro Bolondi, Adriano Kretzmer, Helene Much, Christian Buschow, René Rose, Alina Wu, Hua-Jun Mackowiak, Sebastian D Braendl, Bjoern Giesselmann, Pay Tornisiello, Rosaria Parsi, Krishna Mohan Huey, Jack Mielke, Thorsten Meierhofer, David Maehr, René Hnisz, Denes Michor, Franziska Rinn, John L Meissner, Alexander eLife Cell Biology Long non-coding RNAs (lncRNAs) have emerged as fundamental regulators in various biological processes, including embryonic development and cellular differentiation. Despite much progress over the past decade, the genome-wide annotation of lncRNAs remains incomplete and many known non-coding loci are still poorly characterized. Here, we report the discovery of a previously unannotated lncRNA that is transcribed 230 kb upstream of the SOX17 gene and located within the same topologically associating domain. We termed it T-REX17 (Transcript Regulating Endoderm and activated by soX17) and show that it is induced following SOX17 activation but its expression is more tightly restricted to early definitive endoderm. Loss of T-REX17 affects crucial functions independent of SOX17 and leads to an aberrant endodermal transcriptome, signaling pathway deregulation and epithelial to mesenchymal transition defects. Consequently, cells lacking the lncRNA cannot further differentiate into more mature endodermal cell types. Taken together, our study identified and characterized T-REX17 as a transiently expressed and essential non-coding regulator in early human endoderm differentiation. eLife Sciences Publications, Ltd 2023-01-31 /pmc/articles/PMC9889090/ /pubmed/36719724 http://dx.doi.org/10.7554/eLife.83077 Text en © 2023, Landshammer, Bolondi et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Landshammer, Alexandro Bolondi, Adriano Kretzmer, Helene Much, Christian Buschow, René Rose, Alina Wu, Hua-Jun Mackowiak, Sebastian D Braendl, Bjoern Giesselmann, Pay Tornisiello, Rosaria Parsi, Krishna Mohan Huey, Jack Mielke, Thorsten Meierhofer, David Maehr, René Hnisz, Denes Michor, Franziska Rinn, John L Meissner, Alexander T-REX17 is a transiently expressed non-coding RNA essential for human endoderm formation |
title | T-REX17 is a transiently expressed non-coding RNA essential for human endoderm formation |
title_full | T-REX17 is a transiently expressed non-coding RNA essential for human endoderm formation |
title_fullStr | T-REX17 is a transiently expressed non-coding RNA essential for human endoderm formation |
title_full_unstemmed | T-REX17 is a transiently expressed non-coding RNA essential for human endoderm formation |
title_short | T-REX17 is a transiently expressed non-coding RNA essential for human endoderm formation |
title_sort | t-rex17 is a transiently expressed non-coding rna essential for human endoderm formation |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889090/ https://www.ncbi.nlm.nih.gov/pubmed/36719724 http://dx.doi.org/10.7554/eLife.83077 |
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