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Programmable mutually exclusive alternative splicing for generating RNA and protein diversity
Alternative splicing performs a central role in expanding genomic coding capacity and proteomic diversity. However, programming of splicing patterns in engineered biological systems remains underused. Synthetic approaches thus far have predominantly focused on controlling expression of a single prot...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572816/ https://www.ncbi.nlm.nih.gov/pubmed/31209208 http://dx.doi.org/10.1038/s41467-019-10403-w |
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author | Mathur, Melina Kim, Cameron M. Munro, Sarah A. Rudina, Shireen S. Sawyer, Eric M. Smolke, Christina D. |
author_facet | Mathur, Melina Kim, Cameron M. Munro, Sarah A. Rudina, Shireen S. Sawyer, Eric M. Smolke, Christina D. |
author_sort | Mathur, Melina |
collection | PubMed |
description | Alternative splicing performs a central role in expanding genomic coding capacity and proteomic diversity. However, programming of splicing patterns in engineered biological systems remains underused. Synthetic approaches thus far have predominantly focused on controlling expression of a single protein through alternative splicing. Here, we describe a modular and extensible platform for regulating four programmable exons that undergo a mutually exclusive alternative splicing event to generate multiple functionally-distinct proteins. We present an intron framework that enforces the mutual exclusivity of two internal exons and demonstrate a graded series of consensus sequence elements of varying strengths that set the ratio of two mutually exclusive isoforms. We apply this framework to program the DNA-binding domains of modular transcription factors to differentially control downstream gene activation. This splicing platform advances an approach for generating diverse isoforms and can ultimately be applied to program modular proteins and increase coding capacity of synthetic biological systems. |
format | Online Article Text |
id | pubmed-6572816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65728162019-06-24 Programmable mutually exclusive alternative splicing for generating RNA and protein diversity Mathur, Melina Kim, Cameron M. Munro, Sarah A. Rudina, Shireen S. Sawyer, Eric M. Smolke, Christina D. Nat Commun Article Alternative splicing performs a central role in expanding genomic coding capacity and proteomic diversity. However, programming of splicing patterns in engineered biological systems remains underused. Synthetic approaches thus far have predominantly focused on controlling expression of a single protein through alternative splicing. Here, we describe a modular and extensible platform for regulating four programmable exons that undergo a mutually exclusive alternative splicing event to generate multiple functionally-distinct proteins. We present an intron framework that enforces the mutual exclusivity of two internal exons and demonstrate a graded series of consensus sequence elements of varying strengths that set the ratio of two mutually exclusive isoforms. We apply this framework to program the DNA-binding domains of modular transcription factors to differentially control downstream gene activation. This splicing platform advances an approach for generating diverse isoforms and can ultimately be applied to program modular proteins and increase coding capacity of synthetic biological systems. Nature Publishing Group UK 2019-06-17 /pmc/articles/PMC6572816/ /pubmed/31209208 http://dx.doi.org/10.1038/s41467-019-10403-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mathur, Melina Kim, Cameron M. Munro, Sarah A. Rudina, Shireen S. Sawyer, Eric M. Smolke, Christina D. Programmable mutually exclusive alternative splicing for generating RNA and protein diversity |
title | Programmable mutually exclusive alternative splicing for generating RNA and protein diversity |
title_full | Programmable mutually exclusive alternative splicing for generating RNA and protein diversity |
title_fullStr | Programmable mutually exclusive alternative splicing for generating RNA and protein diversity |
title_full_unstemmed | Programmable mutually exclusive alternative splicing for generating RNA and protein diversity |
title_short | Programmable mutually exclusive alternative splicing for generating RNA and protein diversity |
title_sort | programmable mutually exclusive alternative splicing for generating rna and protein diversity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572816/ https://www.ncbi.nlm.nih.gov/pubmed/31209208 http://dx.doi.org/10.1038/s41467-019-10403-w |
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