Cargando…
Design of synthetic epigenetic circuits featuring memory effects and reversible switching based on DNA methylation
Epigenetic systems store information in DNA methylation patterns in a durable but reversible manner, but have not been regularly used in synthetic biology. Here, we designed synthetic epigenetic memory systems using DNA methylation sensitive engineered zinc finger proteins to repress a memory operon...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458116/ https://www.ncbi.nlm.nih.gov/pubmed/28537256 http://dx.doi.org/10.1038/ncomms15336 |
_version_ | 1783241688833064960 |
---|---|
author | Maier, Johannes A. H. Möhrle, Raphael Jeltsch, Albert |
author_facet | Maier, Johannes A. H. Möhrle, Raphael Jeltsch, Albert |
author_sort | Maier, Johannes A. H. |
collection | PubMed |
description | Epigenetic systems store information in DNA methylation patterns in a durable but reversible manner, but have not been regularly used in synthetic biology. Here, we designed synthetic epigenetic memory systems using DNA methylation sensitive engineered zinc finger proteins to repress a memory operon comprising the CcrM methyltransferase and a reporter. Triggering by heat, nutrients, ultraviolet irradiation or DNA damaging compounds induces CcrM expression and DNA methylation. In the induced on-state, methylation in the operator of the memory operon prevents zinc finger protein binding leading to positive feedback and permanent activation. Using an mf-Lon protease degradable CcrM variant enables reversible switching. Epigenetic memory systems have numerous potential applications in synthetic biology, including life biosensors, death switches or induction systems for industrial protein production. The large variety of bacterial DNA methyltransferases potentially allows for massive multiplexing of signal storage and logical operations depending on more than one input signal. |
format | Online Article Text |
id | pubmed-5458116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54581162017-07-11 Design of synthetic epigenetic circuits featuring memory effects and reversible switching based on DNA methylation Maier, Johannes A. H. Möhrle, Raphael Jeltsch, Albert Nat Commun Article Epigenetic systems store information in DNA methylation patterns in a durable but reversible manner, but have not been regularly used in synthetic biology. Here, we designed synthetic epigenetic memory systems using DNA methylation sensitive engineered zinc finger proteins to repress a memory operon comprising the CcrM methyltransferase and a reporter. Triggering by heat, nutrients, ultraviolet irradiation or DNA damaging compounds induces CcrM expression and DNA methylation. In the induced on-state, methylation in the operator of the memory operon prevents zinc finger protein binding leading to positive feedback and permanent activation. Using an mf-Lon protease degradable CcrM variant enables reversible switching. Epigenetic memory systems have numerous potential applications in synthetic biology, including life biosensors, death switches or induction systems for industrial protein production. The large variety of bacterial DNA methyltransferases potentially allows for massive multiplexing of signal storage and logical operations depending on more than one input signal. Nature Publishing Group 2017-05-24 /pmc/articles/PMC5458116/ /pubmed/28537256 http://dx.doi.org/10.1038/ncomms15336 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 Maier, Johannes A. H. Möhrle, Raphael Jeltsch, Albert Design of synthetic epigenetic circuits featuring memory effects and reversible switching based on DNA methylation |
title | Design of synthetic epigenetic circuits featuring memory effects and reversible switching based on DNA methylation |
title_full | Design of synthetic epigenetic circuits featuring memory effects and reversible switching based on DNA methylation |
title_fullStr | Design of synthetic epigenetic circuits featuring memory effects and reversible switching based on DNA methylation |
title_full_unstemmed | Design of synthetic epigenetic circuits featuring memory effects and reversible switching based on DNA methylation |
title_short | Design of synthetic epigenetic circuits featuring memory effects and reversible switching based on DNA methylation |
title_sort | design of synthetic epigenetic circuits featuring memory effects and reversible switching based on dna methylation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458116/ https://www.ncbi.nlm.nih.gov/pubmed/28537256 http://dx.doi.org/10.1038/ncomms15336 |
work_keys_str_mv | AT maierjohannesah designofsyntheticepigeneticcircuitsfeaturingmemoryeffectsandreversibleswitchingbasedondnamethylation AT mohrleraphael designofsyntheticepigeneticcircuitsfeaturingmemoryeffectsandreversibleswitchingbasedondnamethylation AT jeltschalbert designofsyntheticepigeneticcircuitsfeaturingmemoryeffectsandreversibleswitchingbasedondnamethylation |