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Identification of Rhythmically Expressed LncRNAs in the Zebrafish Pineal Gland and Testis

Noncoding RNAs have been known to contribute to a variety of fundamental life processes, such as development, metabolism, and circadian rhythms. However, much remains unrevealed in the huge noncoding RNA datasets, which require further bioinformatic analysis and experimental investigation—and in par...

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Autores principales: Mishra, Shital Kumar, Liu, Taole, Wang, Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346003/
https://www.ncbi.nlm.nih.gov/pubmed/34360576
http://dx.doi.org/10.3390/ijms22157810
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author Mishra, Shital Kumar
Liu, Taole
Wang, Han
author_facet Mishra, Shital Kumar
Liu, Taole
Wang, Han
author_sort Mishra, Shital Kumar
collection PubMed
description Noncoding RNAs have been known to contribute to a variety of fundamental life processes, such as development, metabolism, and circadian rhythms. However, much remains unrevealed in the huge noncoding RNA datasets, which require further bioinformatic analysis and experimental investigation—and in particular, the coding potential of lncRNAs and the functions of lncRNA-encoded peptides have not been comprehensively studied to date. Through integrating the time-course experimentation with state-of-the-art computational techniques, we studied tens of thousands of zebrafish lncRNAs from our own experiments and from a published study including time-series transcriptome analyses of the testis and the pineal gland. Rhythmicity analysis of these data revealed approximately 700 rhythmically expressed lncRNAs from the pineal gland and the testis, and their GO, COG, and KEGG pathway functions were analyzed. Comparative and conservative analyses determined 14 rhythmically expressed lncRNAs shared between both the pineal gland and the testis, and 15 pineal gland lncRNAs as well as 3 testis lncRNAs conserved among zebrafish, mice, and humans. Further, we computationally analyzed the conserved lncRNA-encoded peptides, and revealed three pineal gland and one testis lncRNA-encoded peptides conserved among these three species, which were further investigated for their three-dimensional (3D) structures and potential functions. Our computational findings provided novel annotations and regulatory mechanisms for hundreds of rhythmically expressed pineal gland and testis lncRNAs in zebrafish, and set the stage for their experimental studies in the near future.
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spelling pubmed-83460032021-08-07 Identification of Rhythmically Expressed LncRNAs in the Zebrafish Pineal Gland and Testis Mishra, Shital Kumar Liu, Taole Wang, Han Int J Mol Sci Article Noncoding RNAs have been known to contribute to a variety of fundamental life processes, such as development, metabolism, and circadian rhythms. However, much remains unrevealed in the huge noncoding RNA datasets, which require further bioinformatic analysis and experimental investigation—and in particular, the coding potential of lncRNAs and the functions of lncRNA-encoded peptides have not been comprehensively studied to date. Through integrating the time-course experimentation with state-of-the-art computational techniques, we studied tens of thousands of zebrafish lncRNAs from our own experiments and from a published study including time-series transcriptome analyses of the testis and the pineal gland. Rhythmicity analysis of these data revealed approximately 700 rhythmically expressed lncRNAs from the pineal gland and the testis, and their GO, COG, and KEGG pathway functions were analyzed. Comparative and conservative analyses determined 14 rhythmically expressed lncRNAs shared between both the pineal gland and the testis, and 15 pineal gland lncRNAs as well as 3 testis lncRNAs conserved among zebrafish, mice, and humans. Further, we computationally analyzed the conserved lncRNA-encoded peptides, and revealed three pineal gland and one testis lncRNA-encoded peptides conserved among these three species, which were further investigated for their three-dimensional (3D) structures and potential functions. Our computational findings provided novel annotations and regulatory mechanisms for hundreds of rhythmically expressed pineal gland and testis lncRNAs in zebrafish, and set the stage for their experimental studies in the near future. MDPI 2021-07-22 /pmc/articles/PMC8346003/ /pubmed/34360576 http://dx.doi.org/10.3390/ijms22157810 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mishra, Shital Kumar
Liu, Taole
Wang, Han
Identification of Rhythmically Expressed LncRNAs in the Zebrafish Pineal Gland and Testis
title Identification of Rhythmically Expressed LncRNAs in the Zebrafish Pineal Gland and Testis
title_full Identification of Rhythmically Expressed LncRNAs in the Zebrafish Pineal Gland and Testis
title_fullStr Identification of Rhythmically Expressed LncRNAs in the Zebrafish Pineal Gland and Testis
title_full_unstemmed Identification of Rhythmically Expressed LncRNAs in the Zebrafish Pineal Gland and Testis
title_short Identification of Rhythmically Expressed LncRNAs in the Zebrafish Pineal Gland and Testis
title_sort identification of rhythmically expressed lncrnas in the zebrafish pineal gland and testis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346003/
https://www.ncbi.nlm.nih.gov/pubmed/34360576
http://dx.doi.org/10.3390/ijms22157810
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