Content area

Abstract

We describe a synthetic genetic circuit for controlling asymmetric cell division in Escherichia coli in which a progenitor cell creates a differentiated daughter cell while retaining its original phenotype. Specifically, we engineered an inducible system that can bind and segregate plasmid DNA to a single position in the cell. Upon cell division, colocalized plasmids are kept by one and only one of the daughter cells. The other daughter cell receives no plasmid DNA and is irreversibly differentiated from its sibling. In this way, we achieved asymmetric cell division through asymmetric plasmid partitioning. We then used this system to achieve physical separation of genetically distinct cells by tying motility to differentiation. Finally, we characterized an orthogonal inducible circuit that enables the simultaneous asymmetric partitioning of two plasmid species, resulting in cells that have four distinct differentiated states. These results point the way toward the engineering of multicellular systems from prokaryotic hosts.

Details

Title
A synthetic system for asymmetric cell division in Escherichia coli
Author
Molinari, Sara 1 ; Shis, David L 2 ; Bhakta, Shyam P 1   VIAFID ORCID Logo  ; Chappell, James 1 ; Igoshin, Oleg A 3   VIAFID ORCID Logo  ; Bennett, Matthew R 4   VIAFID ORCID Logo 

 Department of Biosciences, Rice University, Houston, TX, USA; PhD Program in Systems, Synthetic, and Physical Biology, Rice University, Houston, TX, USA 
 Department of Biosciences, Rice University, Houston, TX, USA 
 Department of Biosciences, Rice University, Houston, TX, USA; Department of Bioengineering, Rice University, Houston, TX, USA; Center for Theoretical Biological Physics, Rice University, Houston, TX, USA 
 Department of Biosciences, Rice University, Houston, TX, USA; PhD Program in Systems, Synthetic, and Physical Biology, Rice University, Houston, TX, USA; Department of Bioengineering, Rice University, Houston, TX, USA 
Pages
917-924
Publication year
2019
Publication date
Sep 2019
Publisher
Nature Publishing Group
ISSN
15524450
e-ISSN
15524469
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2275917697
Copyright
Copyright Nature Publishing Group Sep 2019