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Trans-splicing of mRNAs links gene transcription to translational control regulated by mTOR
GB. Danks, H. Galbiati, M. Raasholm, YN. Torres Cleuren, E. Valen, P. Navratilova, EM. Thompson,
Language English Country Great Britain
Document type Journal Article
Grant support
183690/S10 NFR-FUGE
Norges Forskningsråd
133335/V40
Norges Forskningsråd
NLK
BioMedCentral
from 2000-12-01
BioMedCentral Open Access
from 2000
Directory of Open Access Journals
from 2000
Free Medical Journals
from 2000
PubMed Central
from 2000
Europe PubMed Central
from 2000 to 2020
ProQuest Central
from 2009-01-01
Open Access Digital Library
from 2000-07-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2000-01-01
Medline Complete (EBSCOhost)
from 2000-01-01
Health & Medicine (ProQuest)
from 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
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Springer Nature OA/Free Journals
from 2000-12-01
- MeSH
- Caenorhabditis elegans genetics growth & development MeSH
- Transcription, Genetic * MeSH
- RNA, Messenger chemistry metabolism MeSH
- Nucleotide Motifs MeSH
- Oocytes metabolism MeSH
- Protein Biosynthesis * MeSH
- Gene Expression Regulation * MeSH
- Mammals genetics MeSH
- TOR Serine-Threonine Kinases antagonists & inhibitors metabolism MeSH
- Trans-Splicing * MeSH
- Urochordata genetics MeSH
- Animals MeSH
- Check Tag
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
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.
References provided by Crossref.org
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