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Inducible Control of mRNA Transport Using Reprogrammable RNA-Binding Proteins

[Image: see text] Localization of mRNA is important in a number of cellular processes such as embryogenesis, cellular motility, polarity, and a variety of neurological processes. A synthetic device that controls cellular mRNA localization would facilitate investigations on the significance of mRNA l...

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Autores principales: Abil, Zhanar, Gumy, Laura F., Zhao, Huimin, Hoogenraad, Casper C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477001/
https://www.ncbi.nlm.nih.gov/pubmed/28260376
http://dx.doi.org/10.1021/acssynbio.7b00025
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author Abil, Zhanar
Gumy, Laura F.
Zhao, Huimin
Hoogenraad, Casper C.
author_facet Abil, Zhanar
Gumy, Laura F.
Zhao, Huimin
Hoogenraad, Casper C.
author_sort Abil, Zhanar
collection PubMed
description [Image: see text] Localization of mRNA is important in a number of cellular processes such as embryogenesis, cellular motility, polarity, and a variety of neurological processes. A synthetic device that controls cellular mRNA localization would facilitate investigations on the significance of mRNA localization in cellular function and allow an additional level of controlling gene expression. In this work, we developed the PUF (Pumilio and FBF homology domain)-assisted localization of RNA (PULR) system, which utilizes a eukaryotic cell’s cytoskeletal transport machinery to reposition mRNA within a cell. Depending on the cellular motor used, we show ligand-dependent transport of mRNA toward either pole of the microtubular network of cultured cells. In addition, implementation of the reprogrammable PUF domain allowed the transport of untagged endogenous mRNA in primary neurons.
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spelling pubmed-54770012017-06-21 Inducible Control of mRNA Transport Using Reprogrammable RNA-Binding Proteins Abil, Zhanar Gumy, Laura F. Zhao, Huimin Hoogenraad, Casper C. ACS Synth Biol [Image: see text] Localization of mRNA is important in a number of cellular processes such as embryogenesis, cellular motility, polarity, and a variety of neurological processes. A synthetic device that controls cellular mRNA localization would facilitate investigations on the significance of mRNA localization in cellular function and allow an additional level of controlling gene expression. In this work, we developed the PUF (Pumilio and FBF homology domain)-assisted localization of RNA (PULR) system, which utilizes a eukaryotic cell’s cytoskeletal transport machinery to reposition mRNA within a cell. Depending on the cellular motor used, we show ligand-dependent transport of mRNA toward either pole of the microtubular network of cultured cells. In addition, implementation of the reprogrammable PUF domain allowed the transport of untagged endogenous mRNA in primary neurons. American Chemical Society 2017-03-06 2017-06-16 /pmc/articles/PMC5477001/ /pubmed/28260376 http://dx.doi.org/10.1021/acssynbio.7b00025 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Abil, Zhanar
Gumy, Laura F.
Zhao, Huimin
Hoogenraad, Casper C.
Inducible Control of mRNA Transport Using Reprogrammable RNA-Binding Proteins
title Inducible Control of mRNA Transport Using Reprogrammable RNA-Binding Proteins
title_full Inducible Control of mRNA Transport Using Reprogrammable RNA-Binding Proteins
title_fullStr Inducible Control of mRNA Transport Using Reprogrammable RNA-Binding Proteins
title_full_unstemmed Inducible Control of mRNA Transport Using Reprogrammable RNA-Binding Proteins
title_short Inducible Control of mRNA Transport Using Reprogrammable RNA-Binding Proteins
title_sort inducible control of mrna transport using reprogrammable rna-binding proteins
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477001/
https://www.ncbi.nlm.nih.gov/pubmed/28260376
http://dx.doi.org/10.1021/acssynbio.7b00025
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