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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Online Access: | https://doi.org/10.1371/journal.pone.0232046 |
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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 |
work_keys_str_mv |
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1714804002779037696 |