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Functional analysis of RNA motifs essential for BC200 RNA-mediated translational regulation

Brain cytoplasmic 200 RNA (BC200 RNA) is proposed to act as a local translational modulator by inhibiting translation after being targeted to neuronal dendrites. However, the mechanism by which BC200 RNA inhibits translation is not fully understood. Although a detailed functional analysis of RNA mot...

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Detalles Bibliográficos
Autores principales: Jang, Seonghui, Shin, Heegwon, Lee, Younghoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061212/
https://www.ncbi.nlm.nih.gov/pubmed/31234958
http://dx.doi.org/10.5483/BMBRep.2020.53.2.153
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author Jang, Seonghui
Shin, Heegwon
Lee, Younghoon
author_facet Jang, Seonghui
Shin, Heegwon
Lee, Younghoon
author_sort Jang, Seonghui
collection PubMed
description Brain cytoplasmic 200 RNA (BC200 RNA) is proposed to act as a local translational modulator by inhibiting translation after being targeted to neuronal dendrites. However, the mechanism by which BC200 RNA inhibits translation is not fully understood. Although a detailed functional analysis of RNA motifs is essential for understanding the BC200 RNA-mediated translation-inhibition mechanism, there is little relevant research on the subject. Here, we performed a systematic domain-dissection analysis of BC200 RNA to identify functional RNA motifs responsible for its translational-inhibition activity. Various RNA variants were assayed for their ability to inhibit translation of luciferase mRNA in vitro. We found that the 111–200-nucleotide region consisting of part of the Alu domain as well as the A/C-rich domain (consisting of both the A-rich and C-rich domains) is most effective for translation inhibition. Surprisingly, we also found that individual A-rich, A/C-rich, and Alu domains can enhance translation but at different levels for each domain, and that these enhancing effects manifest as cap-dependent translation.
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spelling pubmed-70612122020-03-19 Functional analysis of RNA motifs essential for BC200 RNA-mediated translational regulation Jang, Seonghui Shin, Heegwon Lee, Younghoon BMB Rep Article Brain cytoplasmic 200 RNA (BC200 RNA) is proposed to act as a local translational modulator by inhibiting translation after being targeted to neuronal dendrites. However, the mechanism by which BC200 RNA inhibits translation is not fully understood. Although a detailed functional analysis of RNA motifs is essential for understanding the BC200 RNA-mediated translation-inhibition mechanism, there is little relevant research on the subject. Here, we performed a systematic domain-dissection analysis of BC200 RNA to identify functional RNA motifs responsible for its translational-inhibition activity. Various RNA variants were assayed for their ability to inhibit translation of luciferase mRNA in vitro. We found that the 111–200-nucleotide region consisting of part of the Alu domain as well as the A/C-rich domain (consisting of both the A-rich and C-rich domains) is most effective for translation inhibition. Surprisingly, we also found that individual A-rich, A/C-rich, and Alu domains can enhance translation but at different levels for each domain, and that these enhancing effects manifest as cap-dependent translation. Korean Society for Biochemistry and Molecular Biology 2020-02-29 2020-02-29 /pmc/articles/PMC7061212/ /pubmed/31234958 http://dx.doi.org/10.5483/BMBRep.2020.53.2.153 Text en Copyright © 2020 by the The Korean Society for Biochemistry and Molecular Biology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Jang, Seonghui
Shin, Heegwon
Lee, Younghoon
Functional analysis of RNA motifs essential for BC200 RNA-mediated translational regulation
title Functional analysis of RNA motifs essential for BC200 RNA-mediated translational regulation
title_full Functional analysis of RNA motifs essential for BC200 RNA-mediated translational regulation
title_fullStr Functional analysis of RNA motifs essential for BC200 RNA-mediated translational regulation
title_full_unstemmed Functional analysis of RNA motifs essential for BC200 RNA-mediated translational regulation
title_short Functional analysis of RNA motifs essential for BC200 RNA-mediated translational regulation
title_sort functional analysis of rna motifs essential for bc200 rna-mediated translational regulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061212/
https://www.ncbi.nlm.nih.gov/pubmed/31234958
http://dx.doi.org/10.5483/BMBRep.2020.53.2.153
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