Cargando…
Orthogonality and Burdens of Heterologous AND Gate Gene Circuits in E. coli
[Image: see text] Synthetic biology approaches commonly introduce heterologous gene networks into a host to predictably program cells, with the expectation of the synthetic network being orthogonal to the host background. However, introduced circuits may interfere with the host’s physiology, either...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820654/ https://www.ncbi.nlm.nih.gov/pubmed/29240998 http://dx.doi.org/10.1021/acssynbio.7b00328 |
_version_ | 1783301415375994880 |
---|---|
author | Liu, Qijun Schumacher, Jörg Wan, Xinyi Lou, Chunbo Wang, Baojun |
author_facet | Liu, Qijun Schumacher, Jörg Wan, Xinyi Lou, Chunbo Wang, Baojun |
author_sort | Liu, Qijun |
collection | PubMed |
description | [Image: see text] Synthetic biology approaches commonly introduce heterologous gene networks into a host to predictably program cells, with the expectation of the synthetic network being orthogonal to the host background. However, introduced circuits may interfere with the host’s physiology, either indirectly by posing a metabolic burden and/or through unintended direct interactions between parts of the circuit with those of the host, affecting functionality. Here we used RNA-Seq transcriptome analysis to quantify the interactions between a representative heterologous AND gate circuit and the host Escherichia coli under various conditions including circuit designs and plasmid copy numbers. We show that the circuit plasmid copy number outweighs circuit composition for their effect on host gene expression with medium-copy number plasmid showing more prominent interference than its low-copy number counterpart. In contrast, the circuits have a stronger influence on the host growth with a metabolic load increasing with the copy number of the circuits. Notably, we show that variation of copy number, an increase from low to medium copy, caused different types of change observed in the behavior of components in the AND gate circuit leading to the unbalance of the two gate-inputs and thus counterintuitive output attenuation. The study demonstrates the circuit plasmid copy number is a key factor that can dramatically affect the orthogonality, burden and functionality of the heterologous circuits in the host chassis. The results provide important guidance for future efforts to design orthogonal and robust gene circuits with minimal unwanted interaction and burden to their host. |
format | Online Article Text |
id | pubmed-5820654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-58206542018-02-26 Orthogonality and Burdens of Heterologous AND Gate Gene Circuits in E. coli Liu, Qijun Schumacher, Jörg Wan, Xinyi Lou, Chunbo Wang, Baojun ACS Synth Biol [Image: see text] Synthetic biology approaches commonly introduce heterologous gene networks into a host to predictably program cells, with the expectation of the synthetic network being orthogonal to the host background. However, introduced circuits may interfere with the host’s physiology, either indirectly by posing a metabolic burden and/or through unintended direct interactions between parts of the circuit with those of the host, affecting functionality. Here we used RNA-Seq transcriptome analysis to quantify the interactions between a representative heterologous AND gate circuit and the host Escherichia coli under various conditions including circuit designs and plasmid copy numbers. We show that the circuit plasmid copy number outweighs circuit composition for their effect on host gene expression with medium-copy number plasmid showing more prominent interference than its low-copy number counterpart. In contrast, the circuits have a stronger influence on the host growth with a metabolic load increasing with the copy number of the circuits. Notably, we show that variation of copy number, an increase from low to medium copy, caused different types of change observed in the behavior of components in the AND gate circuit leading to the unbalance of the two gate-inputs and thus counterintuitive output attenuation. The study demonstrates the circuit plasmid copy number is a key factor that can dramatically affect the orthogonality, burden and functionality of the heterologous circuits in the host chassis. The results provide important guidance for future efforts to design orthogonal and robust gene circuits with minimal unwanted interaction and burden to their host. American Chemical Society 2017-12-14 2018-02-16 /pmc/articles/PMC5820654/ /pubmed/29240998 http://dx.doi.org/10.1021/acssynbio.7b00328 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Liu, Qijun Schumacher, Jörg Wan, Xinyi Lou, Chunbo Wang, Baojun Orthogonality and Burdens of Heterologous AND Gate Gene Circuits in E. coli |
title | Orthogonality and Burdens of Heterologous AND Gate
Gene Circuits in E. coli |
title_full | Orthogonality and Burdens of Heterologous AND Gate
Gene Circuits in E. coli |
title_fullStr | Orthogonality and Burdens of Heterologous AND Gate
Gene Circuits in E. coli |
title_full_unstemmed | Orthogonality and Burdens of Heterologous AND Gate
Gene Circuits in E. coli |
title_short | Orthogonality and Burdens of Heterologous AND Gate
Gene Circuits in E. coli |
title_sort | orthogonality and burdens of heterologous and gate
gene circuits in e. coli |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820654/ https://www.ncbi.nlm.nih.gov/pubmed/29240998 http://dx.doi.org/10.1021/acssynbio.7b00328 |
work_keys_str_mv | AT liuqijun orthogonalityandburdensofheterologousandgategenecircuitsinecoli AT schumacherjorg orthogonalityandburdensofheterologousandgategenecircuitsinecoli AT wanxinyi orthogonalityandburdensofheterologousandgategenecircuitsinecoli AT louchunbo orthogonalityandburdensofheterologousandgategenecircuitsinecoli AT wangbaojun orthogonalityandburdensofheterologousandgategenecircuitsinecoli |