Tunable self-cleaving ribozymes for modulating gene expression in eukaryotic systems.

Advancements in the field of synthetic biology have been possible due to the development of genetic tools that are able to regulate gene expression. However, the current toolbox of gene regulatory tools for eukaryotic systems have been outpaced by those developed for simple, single-celled systems. H...

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Main Authors: Thomas Jacobsen, Gloria Yi, Hadel Al Asafen, Ashley A Jermusyk, Chase L Beisel, Gregory T Reeves
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0232046
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spelling doaj-189166a4f6f946448f7a817bc12079132021-03-04T11:18:18ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01154e023204610.1371/journal.pone.0232046Tunable self-cleaving ribozymes for modulating gene expression in eukaryotic systems.Thomas JacobsenGloria YiHadel Al AsafenAshley A JermusykChase L BeiselGregory T ReevesAdvancements in the field of synthetic biology have been possible due to the development of genetic tools that are able to regulate gene expression. However, the current toolbox of gene regulatory tools for eukaryotic systems have been outpaced by those developed for simple, single-celled systems. Here, we engineered a set of gene regulatory tools by combining self-cleaving ribozymes with various upstream competing sequences that were designed to disrupt ribozyme self-cleavage. As a proof-of-concept, we were able to modulate GFP expression in mammalian cells, and then showed the feasibility of these tools in Drosophila embryos. For each system, the fold-reduction of gene expression was influenced by the location of the self-cleaving ribozyme/upstream competing sequence (i.e. 5' vs. 3' untranslated region) and the competing sequence used. Together, this work provides a set of genetic tools that can be used to tune gene expression across various eukaryotic systems.https://doi.org/10.1371/journal.pone.0232046
collection DOAJ
language English
format Article
sources DOAJ
author Thomas Jacobsen
Gloria Yi
Hadel Al Asafen
Ashley A Jermusyk
Chase L Beisel
Gregory T Reeves
spellingShingle Thomas Jacobsen
Gloria Yi
Hadel Al Asafen
Ashley A Jermusyk
Chase L Beisel
Gregory T Reeves
Tunable self-cleaving ribozymes for modulating gene expression in eukaryotic systems.
PLoS ONE
author_facet Thomas Jacobsen
Gloria Yi
Hadel Al Asafen
Ashley A Jermusyk
Chase L Beisel
Gregory T Reeves
author_sort Thomas Jacobsen
title Tunable self-cleaving ribozymes for modulating gene expression in eukaryotic systems.
title_short Tunable self-cleaving ribozymes for modulating gene expression in eukaryotic systems.
title_full Tunable self-cleaving ribozymes for modulating gene expression in eukaryotic systems.
title_fullStr Tunable self-cleaving ribozymes for modulating gene expression in eukaryotic systems.
title_full_unstemmed Tunable self-cleaving ribozymes for modulating gene expression in eukaryotic systems.
title_sort tunable self-cleaving ribozymes for modulating gene expression in eukaryotic systems.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2020-01-01
description Advancements in the field of synthetic biology have been possible due to the development of genetic tools that are able to regulate gene expression. However, the current toolbox of gene regulatory tools for eukaryotic systems have been outpaced by those developed for simple, single-celled systems. Here, we engineered a set of gene regulatory tools by combining self-cleaving ribozymes with various upstream competing sequences that were designed to disrupt ribozyme self-cleavage. As a proof-of-concept, we were able to modulate GFP expression in mammalian cells, and then showed the feasibility of these tools in Drosophila embryos. For each system, the fold-reduction of gene expression was influenced by the location of the self-cleaving ribozyme/upstream competing sequence (i.e. 5' vs. 3' untranslated region) and the competing sequence used. Together, this work provides a set of genetic tools that can be used to tune gene expression across various eukaryotic systems.
url https://doi.org/10.1371/journal.pone.0232046
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