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Functionalization of an Antisense Small RNA

In order to explore the possibility of adding new functions to preexisting genes, we considered a framework of riboregulation. We created a new riboregulator consisting of the reverse complement of a known riboregulator. Using computational design, we engineered a cis-repressing 5′ untranslated regi...

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Autores principales: Rodrigo, Guillermo, Prakash, Satya, Cordero, Teresa, Kushwaha, Manish, Jaramillo, Alfonso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819895/
https://www.ncbi.nlm.nih.gov/pubmed/26756967
http://dx.doi.org/10.1016/j.jmb.2015.12.022
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author Rodrigo, Guillermo
Prakash, Satya
Cordero, Teresa
Kushwaha, Manish
Jaramillo, Alfonso
author_facet Rodrigo, Guillermo
Prakash, Satya
Cordero, Teresa
Kushwaha, Manish
Jaramillo, Alfonso
author_sort Rodrigo, Guillermo
collection PubMed
description In order to explore the possibility of adding new functions to preexisting genes, we considered a framework of riboregulation. We created a new riboregulator consisting of the reverse complement of a known riboregulator. Using computational design, we engineered a cis-repressing 5′ untranslated region that can be activated by this new riboregulator. As a result, both RNAs can orthogonally trans-activate translation of their cognate, independent targets. The two riboregulators can also repress each other by antisense interaction, although not symmetrically. Our work highlights that antisense small RNAs can work as regulatory agents beyond the antisense paradigm and that, hence, they could be interfaced with other circuits used in synthetic biology.
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spelling pubmed-48198952016-04-14 Functionalization of an Antisense Small RNA Rodrigo, Guillermo Prakash, Satya Cordero, Teresa Kushwaha, Manish Jaramillo, Alfonso J Mol Biol Brevia In order to explore the possibility of adding new functions to preexisting genes, we considered a framework of riboregulation. We created a new riboregulator consisting of the reverse complement of a known riboregulator. Using computational design, we engineered a cis-repressing 5′ untranslated region that can be activated by this new riboregulator. As a result, both RNAs can orthogonally trans-activate translation of their cognate, independent targets. The two riboregulators can also repress each other by antisense interaction, although not symmetrically. Our work highlights that antisense small RNAs can work as regulatory agents beyond the antisense paradigm and that, hence, they could be interfaced with other circuits used in synthetic biology. Elsevier 2016-02-27 /pmc/articles/PMC4819895/ /pubmed/26756967 http://dx.doi.org/10.1016/j.jmb.2015.12.022 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Brevia
Rodrigo, Guillermo
Prakash, Satya
Cordero, Teresa
Kushwaha, Manish
Jaramillo, Alfonso
Functionalization of an Antisense Small RNA
title Functionalization of an Antisense Small RNA
title_full Functionalization of an Antisense Small RNA
title_fullStr Functionalization of an Antisense Small RNA
title_full_unstemmed Functionalization of an Antisense Small RNA
title_short Functionalization of an Antisense Small RNA
title_sort functionalization of an antisense small rna
topic Brevia
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819895/
https://www.ncbi.nlm.nih.gov/pubmed/26756967
http://dx.doi.org/10.1016/j.jmb.2015.12.022
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