Cargando…

Trans-splicing of mRNAs links gene transcription to translational control regulated by mTOR

BACKGROUND: In phylogenetically diverse organisms, the 5′ ends of a subset of mRNAs are trans-spliced with a spliced leader (SL) RNA. The functions of SL trans-splicing, however, remain largely enigmatic. RESULTS: We quantified translation genome-wide in the marine chordate, Oikopleura dioica, under...

Descripción completa

Detalles Bibliográficos
Autores principales: Danks, Gemma B., Galbiati, Heloisa, Raasholm, Martina, Torres Cleuren, Yamila N., Valen, Eivind, Navratilova, Pavla, Thompson, Eric M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883708/
https://www.ncbi.nlm.nih.gov/pubmed/31783727
http://dx.doi.org/10.1186/s12864-019-6277-x
_version_ 1783474439043678208
author Danks, Gemma B.
Galbiati, Heloisa
Raasholm, Martina
Torres Cleuren, Yamila N.
Valen, Eivind
Navratilova, Pavla
Thompson, Eric M.
author_facet Danks, Gemma B.
Galbiati, Heloisa
Raasholm, Martina
Torres Cleuren, Yamila N.
Valen, Eivind
Navratilova, Pavla
Thompson, Eric M.
author_sort Danks, Gemma B.
collection PubMed
description BACKGROUND: In phylogenetically diverse organisms, the 5′ ends of a subset of mRNAs are trans-spliced with a spliced leader (SL) RNA. The functions of SL trans-splicing, however, remain largely enigmatic. RESULTS: We quantified translation genome-wide in the marine chordate, Oikopleura dioica, under inhibition of mTOR, a central growth regulator. Translation of trans-spliced TOP mRNAs was suppressed, consistent with a role of the SL sequence in nutrient-dependent translational control of growth-related mRNAs. Under crowded, nutrient-limiting conditions, O. dioica continued to filter-feed, but arrested growth until favorable conditions returned. Upon release from unfavorable conditions, initial recovery was independent of nutrient-responsive, trans-spliced genes, suggesting animal density sensing as a first trigger for resumption of development. CONCLUSION: Our results are consistent with a proposed role of trans-splicing in the coordinated translational down-regulation of nutrient-responsive genes under growth-limiting conditions.
format Online
Article
Text
id pubmed-6883708
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-68837082019-12-03 Trans-splicing of mRNAs links gene transcription to translational control regulated by mTOR Danks, Gemma B. Galbiati, Heloisa Raasholm, Martina Torres Cleuren, Yamila N. Valen, Eivind Navratilova, Pavla Thompson, Eric M. BMC Genomics Research Article BACKGROUND: In phylogenetically diverse organisms, the 5′ ends of a subset of mRNAs are trans-spliced with a spliced leader (SL) RNA. The functions of SL trans-splicing, however, remain largely enigmatic. RESULTS: We quantified translation genome-wide in the marine chordate, Oikopleura dioica, under inhibition of mTOR, a central growth regulator. Translation of trans-spliced TOP mRNAs was suppressed, consistent with a role of the SL sequence in nutrient-dependent translational control of growth-related mRNAs. Under crowded, nutrient-limiting conditions, O. dioica continued to filter-feed, but arrested growth until favorable conditions returned. Upon release from unfavorable conditions, initial recovery was independent of nutrient-responsive, trans-spliced genes, suggesting animal density sensing as a first trigger for resumption of development. CONCLUSION: Our results are consistent with a proposed role of trans-splicing in the coordinated translational down-regulation of nutrient-responsive genes under growth-limiting conditions. BioMed Central 2019-11-29 /pmc/articles/PMC6883708/ /pubmed/31783727 http://dx.doi.org/10.1186/s12864-019-6277-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Danks, Gemma B.
Galbiati, Heloisa
Raasholm, Martina
Torres Cleuren, Yamila N.
Valen, Eivind
Navratilova, Pavla
Thompson, Eric M.
Trans-splicing of mRNAs links gene transcription to translational control regulated by mTOR
title Trans-splicing of mRNAs links gene transcription to translational control regulated by mTOR
title_full Trans-splicing of mRNAs links gene transcription to translational control regulated by mTOR
title_fullStr Trans-splicing of mRNAs links gene transcription to translational control regulated by mTOR
title_full_unstemmed Trans-splicing of mRNAs links gene transcription to translational control regulated by mTOR
title_short Trans-splicing of mRNAs links gene transcription to translational control regulated by mTOR
title_sort trans-splicing of mrnas links gene transcription to translational control regulated by mtor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883708/
https://www.ncbi.nlm.nih.gov/pubmed/31783727
http://dx.doi.org/10.1186/s12864-019-6277-x
work_keys_str_mv AT danksgemmab transsplicingofmrnaslinksgenetranscriptiontotranslationalcontrolregulatedbymtor
AT galbiatiheloisa transsplicingofmrnaslinksgenetranscriptiontotranslationalcontrolregulatedbymtor
AT raasholmmartina transsplicingofmrnaslinksgenetranscriptiontotranslationalcontrolregulatedbymtor
AT torrescleurenyamilan transsplicingofmrnaslinksgenetranscriptiontotranslationalcontrolregulatedbymtor
AT valeneivind transsplicingofmrnaslinksgenetranscriptiontotranslationalcontrolregulatedbymtor
AT navratilovapavla transsplicingofmrnaslinksgenetranscriptiontotranslationalcontrolregulatedbymtor
AT thompsonericm transsplicingofmrnaslinksgenetranscriptiontotranslationalcontrolregulatedbymtor