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Comprehensive analysis of circRNA expression profiles and circRNA‐associated competing endogenous RNA networks in the development of mouse thymus
The thymus plays an irreplaceable role as a primary lymphoid organ. However, the complicate processes of its development and involution are incompletely understood. Accumulating evidence indicates that non‐coding RNAs play key roles in the regulation of biological development. At present, the studie...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294154/ https://www.ncbi.nlm.nih.gov/pubmed/32307889 http://dx.doi.org/10.1111/jcmm.15276 |
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author | Li, Wenting Ma, Nana Yuwen, Ting Yu, Bo Zhou, Yao Yao, Yufei Li, Qi Chen, Xiaofan Wan, Jun Zhang, Yu Zhang, Wei |
author_facet | Li, Wenting Ma, Nana Yuwen, Ting Yu, Bo Zhou, Yao Yao, Yufei Li, Qi Chen, Xiaofan Wan, Jun Zhang, Yu Zhang, Wei |
author_sort | Li, Wenting |
collection | PubMed |
description | The thymus plays an irreplaceable role as a primary lymphoid organ. However, the complicate processes of its development and involution are incompletely understood. Accumulating evidence indicates that non‐coding RNAs play key roles in the regulation of biological development. At present, the studies of the circRNA profiles and of circRNA‐associated competing endogenous RNAs (ceRNAs) in the thymus are still scarce. Here, deep‐RNA sequencing was used to study the biological mechanisms underlying the development process (from 2‐week‐old to 6‐week‐old) and the recession process (from 6‐week‐old to 3‐month‐old) of the mouse thymus. It was found that 196 circRNAs, 233 miRNAs and 3807 mRNAs were significantly dysregulated. The circRNA‐associated ceRNA networks were constructed in the mouse thymus, which were mainly involved in early embryonic development and the proliferation and division of T cells. Taken together, these results elucidated the regulatory roles of ceRNAs in the development and involution processes of the mouse thymus. |
format | Online Article Text |
id | pubmed-7294154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72941542020-06-15 Comprehensive analysis of circRNA expression profiles and circRNA‐associated competing endogenous RNA networks in the development of mouse thymus Li, Wenting Ma, Nana Yuwen, Ting Yu, Bo Zhou, Yao Yao, Yufei Li, Qi Chen, Xiaofan Wan, Jun Zhang, Yu Zhang, Wei J Cell Mol Med Original Articles The thymus plays an irreplaceable role as a primary lymphoid organ. However, the complicate processes of its development and involution are incompletely understood. Accumulating evidence indicates that non‐coding RNAs play key roles in the regulation of biological development. At present, the studies of the circRNA profiles and of circRNA‐associated competing endogenous RNAs (ceRNAs) in the thymus are still scarce. Here, deep‐RNA sequencing was used to study the biological mechanisms underlying the development process (from 2‐week‐old to 6‐week‐old) and the recession process (from 6‐week‐old to 3‐month‐old) of the mouse thymus. It was found that 196 circRNAs, 233 miRNAs and 3807 mRNAs were significantly dysregulated. The circRNA‐associated ceRNA networks were constructed in the mouse thymus, which were mainly involved in early embryonic development and the proliferation and division of T cells. Taken together, these results elucidated the regulatory roles of ceRNAs in the development and involution processes of the mouse thymus. John Wiley and Sons Inc. 2020-04-19 2020-06 /pmc/articles/PMC7294154/ /pubmed/32307889 http://dx.doi.org/10.1111/jcmm.15276 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Li, Wenting Ma, Nana Yuwen, Ting Yu, Bo Zhou, Yao Yao, Yufei Li, Qi Chen, Xiaofan Wan, Jun Zhang, Yu Zhang, Wei Comprehensive analysis of circRNA expression profiles and circRNA‐associated competing endogenous RNA networks in the development of mouse thymus |
title | Comprehensive analysis of circRNA expression profiles and circRNA‐associated competing endogenous RNA networks in the development of mouse thymus |
title_full | Comprehensive analysis of circRNA expression profiles and circRNA‐associated competing endogenous RNA networks in the development of mouse thymus |
title_fullStr | Comprehensive analysis of circRNA expression profiles and circRNA‐associated competing endogenous RNA networks in the development of mouse thymus |
title_full_unstemmed | Comprehensive analysis of circRNA expression profiles and circRNA‐associated competing endogenous RNA networks in the development of mouse thymus |
title_short | Comprehensive analysis of circRNA expression profiles and circRNA‐associated competing endogenous RNA networks in the development of mouse thymus |
title_sort | comprehensive analysis of circrna expression profiles and circrna‐associated competing endogenous rna networks in the development of mouse thymus |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294154/ https://www.ncbi.nlm.nih.gov/pubmed/32307889 http://dx.doi.org/10.1111/jcmm.15276 |
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