SINEUP long non-coding RNA acts via PTBP1 and HNRNPK to promote translational initiation assemblies.


Journal

Nucleic acids research
ISSN: 1362-4962
Titre abrégé: Nucleic Acids Res
Pays: England
ID NLM: 0411011

Informations de publication

Date de publication:
18 11 2020
Historique:
accepted: 23 09 2020
revised: 26 08 2020
received: 04 02 2020
pubmed: 2 11 2020
medline: 4 2 2021
entrez: 1 11 2020
Statut: ppublish

Résumé

SINEUPs are long non-coding RNAs (lncRNAs) that contain a SINE element, and which up-regulate the translation of target mRNA. They have been studied in a wide range of applications, as both biological and therapeutic tools, although the underpinning molecular mechanism is unclear. Here, we focused on the sub-cellular distribution of target mRNAs and SINEUP RNAs, performing co-transfection of expression vectors for these transcripts into human embryonic kidney cells (HEK293T/17), to investigate the network of translational regulation. The results showed that co-localization of target mRNAs and SINEUP RNAs in the cytoplasm was a key phenomenon. We identified PTBP1 and HNRNPK as essential RNA binding proteins. These proteins contributed to SINEUP RNA sub-cellular distribution and to assembly of translational initiation complexes, leading to enhanced target mRNA translation. These findings will promote a better understanding of the mechanisms employed by regulatory RNAs implicated in efficient protein translation.

Identifiants

pubmed: 33130894
pii: 5936032
doi: 10.1093/nar/gkaa814
pmc: PMC7672464
doi:

Substances chimiques

Heterogeneous-Nuclear Ribonucleoprotein K 0
Heterogeneous-Nuclear Ribonucleoproteins 0
PTBP1 protein, human 0
RNA, Long Noncoding 0
RNA-Binding Proteins 0
enhanced green fluorescent protein 0
Polypyrimidine Tract-Binding Protein 139076-35-0
HNRNPK protein, human 146410-60-8
Green Fluorescent Proteins 147336-22-9

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

11626-11644

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research.

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Auteurs

Naoko Toki (N)

Laboratory for Transcriptome Technology, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa 230-0045 Japan.
Functional Genomics Laboratory, Graduate School of Medical Life Science, Yokohama City University, Yokohama, Japan.

Hazuki Takahashi (H)

Laboratory for Transcriptome Technology, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa 230-0045 Japan.
Functional Genomics Laboratory, Graduate School of Medical Life Science, Yokohama City University, Yokohama, Japan.

Harshita Sharma (H)

Laboratory for Transcriptome Technology, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa 230-0045 Japan.

Matthew N Z Valentine (MNZ)

Laboratory for Transcriptome Technology, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa 230-0045 Japan.

Ferdous-Ur M Rahman (FM)

Laboratory for Transcriptome Technology, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa 230-0045 Japan.

Silvia Zucchelli (S)

Department of Health Sciences, Center for Autoimmune and Allergic Diseases (CAAD) and Interdisciplinary Research Center of Autoimmune Diseases (IRCAD), University of Piemonte Orientale, Novara, Italy.

Stefano Gustincich (S)

Department of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, Genova, Italy.

Piero Carninci (P)

Laboratory for Transcriptome Technology, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa 230-0045 Japan.
Functional Genomics Laboratory, Graduate School of Medical Life Science, Yokohama City University, Yokohama, Japan.

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Classifications MeSH