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Improved Combinatorial Assembly and Barcode Sequencing for Gene-Sized DNA Constructs
[Image: see text] Synergistic and supportive interactions among genes can be incorporated in engineering biology to enhance and stabilize the performance of biological systems, but combinatorial numerical explosion challenges the analysis of multigene interactions. The incorporation of DNA barcodes...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510714/ https://www.ncbi.nlm.nih.gov/pubmed/37582217 http://dx.doi.org/10.1021/acssynbio.3c00183 |
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author | Hernandez Hernandez, Diana Ding, Lin Murao, Ayako Dahlin, Lukas R. Li, Gabriella Arnolds, Kathleen L. Amezola, Melissa Klein, Amit Mitra, Aishwarya Mecacci, Sonia Linger, Jeffrey G. Guarnieri, Michael T. Suzuki, Yo |
author_facet | Hernandez Hernandez, Diana Ding, Lin Murao, Ayako Dahlin, Lukas R. Li, Gabriella Arnolds, Kathleen L. Amezola, Melissa Klein, Amit Mitra, Aishwarya Mecacci, Sonia Linger, Jeffrey G. Guarnieri, Michael T. Suzuki, Yo |
author_sort | Hernandez Hernandez, Diana |
collection | PubMed |
description | [Image: see text] Synergistic and supportive interactions among genes can be incorporated in engineering biology to enhance and stabilize the performance of biological systems, but combinatorial numerical explosion challenges the analysis of multigene interactions. The incorporation of DNA barcodes to mark genes coupled with next-generation sequencing offers a solution to this challenge. We describe improvements for a key method in this space, CombiGEM, to broaden its application to assembling typical gene-sized DNA fragments and to reduce the cost of sequencing for prevalent small-scale projects. The expanded reach of the method beyond currently targeted small RNA genes promotes the discovery and incorporation of gene synergy in natural and engineered processes such as biocontainment, the production of desired compounds, and previously uncharacterized fundamental biological mechanisms. |
format | Online Article Text |
id | pubmed-10510714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-105107142023-09-21 Improved Combinatorial Assembly and Barcode Sequencing for Gene-Sized DNA Constructs Hernandez Hernandez, Diana Ding, Lin Murao, Ayako Dahlin, Lukas R. Li, Gabriella Arnolds, Kathleen L. Amezola, Melissa Klein, Amit Mitra, Aishwarya Mecacci, Sonia Linger, Jeffrey G. Guarnieri, Michael T. Suzuki, Yo ACS Synth Biol [Image: see text] Synergistic and supportive interactions among genes can be incorporated in engineering biology to enhance and stabilize the performance of biological systems, but combinatorial numerical explosion challenges the analysis of multigene interactions. The incorporation of DNA barcodes to mark genes coupled with next-generation sequencing offers a solution to this challenge. We describe improvements for a key method in this space, CombiGEM, to broaden its application to assembling typical gene-sized DNA fragments and to reduce the cost of sequencing for prevalent small-scale projects. The expanded reach of the method beyond currently targeted small RNA genes promotes the discovery and incorporation of gene synergy in natural and engineered processes such as biocontainment, the production of desired compounds, and previously uncharacterized fundamental biological mechanisms. American Chemical Society 2023-08-15 /pmc/articles/PMC10510714/ /pubmed/37582217 http://dx.doi.org/10.1021/acssynbio.3c00183 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Hernandez Hernandez, Diana Ding, Lin Murao, Ayako Dahlin, Lukas R. Li, Gabriella Arnolds, Kathleen L. Amezola, Melissa Klein, Amit Mitra, Aishwarya Mecacci, Sonia Linger, Jeffrey G. Guarnieri, Michael T. Suzuki, Yo Improved Combinatorial Assembly and Barcode Sequencing for Gene-Sized DNA Constructs |
title | Improved Combinatorial
Assembly and Barcode Sequencing
for Gene-Sized DNA Constructs |
title_full | Improved Combinatorial
Assembly and Barcode Sequencing
for Gene-Sized DNA Constructs |
title_fullStr | Improved Combinatorial
Assembly and Barcode Sequencing
for Gene-Sized DNA Constructs |
title_full_unstemmed | Improved Combinatorial
Assembly and Barcode Sequencing
for Gene-Sized DNA Constructs |
title_short | Improved Combinatorial
Assembly and Barcode Sequencing
for Gene-Sized DNA Constructs |
title_sort | improved combinatorial
assembly and barcode sequencing
for gene-sized dna constructs |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510714/ https://www.ncbi.nlm.nih.gov/pubmed/37582217 http://dx.doi.org/10.1021/acssynbio.3c00183 |
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