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Expanding the genetic code of Mus musculus
Here we report the expansion of the genetic code of Mus musculus with various unnatural amino acids including N(ɛ)-acetyl-lysine. Stable integration of transgenes encoding an engineered N(ɛ)-acetyl-lysyl-tRNA synthetase (AcKRS)/tRNA(Pyl) pair into the mouse genome enables site-specific incorporation...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5321798/ https://www.ncbi.nlm.nih.gov/pubmed/28220771 http://dx.doi.org/10.1038/ncomms14568 |
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author | Han, Songmi Yang, Aerin Lee, Soonjang Lee, Han-Woong Park, Chan Bae Park, Hee-Sung |
author_facet | Han, Songmi Yang, Aerin Lee, Soonjang Lee, Han-Woong Park, Chan Bae Park, Hee-Sung |
author_sort | Han, Songmi |
collection | PubMed |
description | Here we report the expansion of the genetic code of Mus musculus with various unnatural amino acids including N(ɛ)-acetyl-lysine. Stable integration of transgenes encoding an engineered N(ɛ)-acetyl-lysyl-tRNA synthetase (AcKRS)/tRNA(Pyl) pair into the mouse genome enables site-specific incorporation of unnatural amino acids into a target protein in response to the amber codon. We demonstrate temporal and spatial control of protein acetylation in various organs of the transgenic mouse using a recombinant green fluorescent protein (GFPuv) as a model protein. This strategy will provide a powerful tool for systematic in vivo study of cellular proteins in the most commonly used mammalian model organism for human physiology and disease. |
format | Online Article Text |
id | pubmed-5321798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53217982017-03-01 Expanding the genetic code of Mus musculus Han, Songmi Yang, Aerin Lee, Soonjang Lee, Han-Woong Park, Chan Bae Park, Hee-Sung Nat Commun Article Here we report the expansion of the genetic code of Mus musculus with various unnatural amino acids including N(ɛ)-acetyl-lysine. Stable integration of transgenes encoding an engineered N(ɛ)-acetyl-lysyl-tRNA synthetase (AcKRS)/tRNA(Pyl) pair into the mouse genome enables site-specific incorporation of unnatural amino acids into a target protein in response to the amber codon. We demonstrate temporal and spatial control of protein acetylation in various organs of the transgenic mouse using a recombinant green fluorescent protein (GFPuv) as a model protein. This strategy will provide a powerful tool for systematic in vivo study of cellular proteins in the most commonly used mammalian model organism for human physiology and disease. Nature Publishing Group 2017-02-21 /pmc/articles/PMC5321798/ /pubmed/28220771 http://dx.doi.org/10.1038/ncomms14568 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Han, Songmi Yang, Aerin Lee, Soonjang Lee, Han-Woong Park, Chan Bae Park, Hee-Sung Expanding the genetic code of Mus musculus |
title | Expanding the genetic code of Mus musculus |
title_full | Expanding the genetic code of Mus musculus |
title_fullStr | Expanding the genetic code of Mus musculus |
title_full_unstemmed | Expanding the genetic code of Mus musculus |
title_short | Expanding the genetic code of Mus musculus |
title_sort | expanding the genetic code of mus musculus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5321798/ https://www.ncbi.nlm.nih.gov/pubmed/28220771 http://dx.doi.org/10.1038/ncomms14568 |
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