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Emerging functions of piwi‐interacting RNAs in diseases

PIWI‐interacting RNAs (piRNAs) are recently discovered small non‐coding RNAs consisting of 24‐35 nucleotides, usually including a characteristic 5‐terminal uridine and an adenosine at position 10. PIWI proteins can specifically bind to the unique structure of the 3′ end of piRNAs. In the past, it wa...

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Detalles Bibliográficos
Autores principales: Wang, Kai, Wang, Tao, Gao, Xiang‐Qian, Chen, Xin‐Zhe, Wang, Fei, Zhou, Lu‐Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178273/
https://www.ncbi.nlm.nih.gov/pubmed/33942984
http://dx.doi.org/10.1111/jcmm.16466
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author Wang, Kai
Wang, Tao
Gao, Xiang‐Qian
Chen, Xin‐Zhe
Wang, Fei
Zhou, Lu‐Yu
author_facet Wang, Kai
Wang, Tao
Gao, Xiang‐Qian
Chen, Xin‐Zhe
Wang, Fei
Zhou, Lu‐Yu
author_sort Wang, Kai
collection PubMed
description PIWI‐interacting RNAs (piRNAs) are recently discovered small non‐coding RNAs consisting of 24‐35 nucleotides, usually including a characteristic 5‐terminal uridine and an adenosine at position 10. PIWI proteins can specifically bind to the unique structure of the 3′ end of piRNAs. In the past, it was thought that piRNAs existed only in the reproductive system, but recently, it was reported that piRNAs are also expressed in several other human tissues with tissue specificity. Growing evidence shows that piRNAs and PIWI proteins are abnormally expressed in various diseases, including cancers, neurodegenerative diseases and ageing, and may be potential biomarkers and therapeutic targets. This review aims to discuss the current research status regarding piRNA biogenetic processes, functions, mechanisms and emerging roles in various diseases.
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spelling pubmed-81782732021-06-15 Emerging functions of piwi‐interacting RNAs in diseases Wang, Kai Wang, Tao Gao, Xiang‐Qian Chen, Xin‐Zhe Wang, Fei Zhou, Lu‐Yu J Cell Mol Med Reviews PIWI‐interacting RNAs (piRNAs) are recently discovered small non‐coding RNAs consisting of 24‐35 nucleotides, usually including a characteristic 5‐terminal uridine and an adenosine at position 10. PIWI proteins can specifically bind to the unique structure of the 3′ end of piRNAs. In the past, it was thought that piRNAs existed only in the reproductive system, but recently, it was reported that piRNAs are also expressed in several other human tissues with tissue specificity. Growing evidence shows that piRNAs and PIWI proteins are abnormally expressed in various diseases, including cancers, neurodegenerative diseases and ageing, and may be potential biomarkers and therapeutic targets. This review aims to discuss the current research status regarding piRNA biogenetic processes, functions, mechanisms and emerging roles in various diseases. John Wiley and Sons Inc. 2021-05-04 2021-06 /pmc/articles/PMC8178273/ /pubmed/33942984 http://dx.doi.org/10.1111/jcmm.16466 Text en © 2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Wang, Kai
Wang, Tao
Gao, Xiang‐Qian
Chen, Xin‐Zhe
Wang, Fei
Zhou, Lu‐Yu
Emerging functions of piwi‐interacting RNAs in diseases
title Emerging functions of piwi‐interacting RNAs in diseases
title_full Emerging functions of piwi‐interacting RNAs in diseases
title_fullStr Emerging functions of piwi‐interacting RNAs in diseases
title_full_unstemmed Emerging functions of piwi‐interacting RNAs in diseases
title_short Emerging functions of piwi‐interacting RNAs in diseases
title_sort emerging functions of piwi‐interacting rnas in diseases
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178273/
https://www.ncbi.nlm.nih.gov/pubmed/33942984
http://dx.doi.org/10.1111/jcmm.16466
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