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Spliced leader RNA trans-splicing discovered in copepods

Copepods are one of the most abundant metazoans in the marine ecosystem, constituting a critical link in aquatic food webs and contributing significantly to the global carbon budget, yet molecular mechanisms of their gene expression are not well understood. Here we report the detection of spliced le...

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Autores principales: Yang, Feifei, Xu, Donghui, Zhuang, Yunyun, Yi, Xiaoyan, Huang, Yousong, Chen, Hongju, Lin, Senjie, Campbell, David A., Sturm, Nancy R., Liu, Guangxing, Zhang, Huan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664967/
https://www.ncbi.nlm.nih.gov/pubmed/26621068
http://dx.doi.org/10.1038/srep17411
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author Yang, Feifei
Xu, Donghui
Zhuang, Yunyun
Yi, Xiaoyan
Huang, Yousong
Chen, Hongju
Lin, Senjie
Campbell, David A.
Sturm, Nancy R.
Liu, Guangxing
Zhang, Huan
author_facet Yang, Feifei
Xu, Donghui
Zhuang, Yunyun
Yi, Xiaoyan
Huang, Yousong
Chen, Hongju
Lin, Senjie
Campbell, David A.
Sturm, Nancy R.
Liu, Guangxing
Zhang, Huan
author_sort Yang, Feifei
collection PubMed
description Copepods are one of the most abundant metazoans in the marine ecosystem, constituting a critical link in aquatic food webs and contributing significantly to the global carbon budget, yet molecular mechanisms of their gene expression are not well understood. Here we report the detection of spliced leader (SL) trans-splicing in calanoid copepods. We have examined nine species of wild-caught copepods from Jiaozhou Bay, China that represent the major families of the calanoids. All these species contained a common 46-nt SL (CopepodSL). We further determined the size of CopepodSL precursor RNA (slRNA; 108-158 nt) through genomic analysis and 3′-RACE technique, which was confirmed by RNA blot analysis. Structure modeling showed that the copepod slRNA folded into typical slRNA secondary structures. Using a CopepodSL-based primer set, we selectively enriched and sequenced copepod full-length cDNAs, which led to the characterization of copepod transcripts and the cataloging of the complete set of 79 eukaryotic cytoplasmic ribosomal proteins (cRPs) for a single copepod species. We uncovered the SL trans-splicing in copepod natural populations, and demonstrated that CopepodSL was a sensitive and specific tool for copepod transcriptomic studies at both the individual and population levels and that it would be useful for metatranscriptomic analysis of copepods.
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spelling pubmed-46649672015-12-03 Spliced leader RNA trans-splicing discovered in copepods Yang, Feifei Xu, Donghui Zhuang, Yunyun Yi, Xiaoyan Huang, Yousong Chen, Hongju Lin, Senjie Campbell, David A. Sturm, Nancy R. Liu, Guangxing Zhang, Huan Sci Rep Article Copepods are one of the most abundant metazoans in the marine ecosystem, constituting a critical link in aquatic food webs and contributing significantly to the global carbon budget, yet molecular mechanisms of their gene expression are not well understood. Here we report the detection of spliced leader (SL) trans-splicing in calanoid copepods. We have examined nine species of wild-caught copepods from Jiaozhou Bay, China that represent the major families of the calanoids. All these species contained a common 46-nt SL (CopepodSL). We further determined the size of CopepodSL precursor RNA (slRNA; 108-158 nt) through genomic analysis and 3′-RACE technique, which was confirmed by RNA blot analysis. Structure modeling showed that the copepod slRNA folded into typical slRNA secondary structures. Using a CopepodSL-based primer set, we selectively enriched and sequenced copepod full-length cDNAs, which led to the characterization of copepod transcripts and the cataloging of the complete set of 79 eukaryotic cytoplasmic ribosomal proteins (cRPs) for a single copepod species. We uncovered the SL trans-splicing in copepod natural populations, and demonstrated that CopepodSL was a sensitive and specific tool for copepod transcriptomic studies at both the individual and population levels and that it would be useful for metatranscriptomic analysis of copepods. Nature Publishing Group 2015-12-01 /pmc/articles/PMC4664967/ /pubmed/26621068 http://dx.doi.org/10.1038/srep17411 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yang, Feifei
Xu, Donghui
Zhuang, Yunyun
Yi, Xiaoyan
Huang, Yousong
Chen, Hongju
Lin, Senjie
Campbell, David A.
Sturm, Nancy R.
Liu, Guangxing
Zhang, Huan
Spliced leader RNA trans-splicing discovered in copepods
title Spliced leader RNA trans-splicing discovered in copepods
title_full Spliced leader RNA trans-splicing discovered in copepods
title_fullStr Spliced leader RNA trans-splicing discovered in copepods
title_full_unstemmed Spliced leader RNA trans-splicing discovered in copepods
title_short Spliced leader RNA trans-splicing discovered in copepods
title_sort spliced leader rna trans-splicing discovered in copepods
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664967/
https://www.ncbi.nlm.nih.gov/pubmed/26621068
http://dx.doi.org/10.1038/srep17411
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