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  4. Expanding applications of portable biological systems: enhancements to mammalian gene editing and bacterial quorum sensing networks
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Expanding applications of portable biological systems: enhancements to mammalian gene editing and bacterial quorum sensing networks

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Description

The portability of genetic tools from one organism to another is a cornerstone of synthetic biology. The shared biological language of DNA-to-RNA-to-protein allows for expression of polypeptide chains in phylogenetically distant organisms with little modification. The tools and contexts are diverse, ranging from catalytic RNAs in cell-free systems to bacterial proteins expressed in human cell lines, yet they exhibit an organizing principle: that genes and proteins may be treated as modular units that can be moved from their native organism to a novel one. However, protein behavior is always unpredictable; drop-in functionality is not guaranteed.

My work characterizes how two different classes of tools behave in new contexts and explores methods to improve their functionality: 1. CRISPR/Cas9 in human cells and 2. quorum sensing networks in Escherichia coli.

1. The genome-editing tool CRISPR/Cas9 has facilitated easily targeted, effective, high throughput genome editing. However, Cas9 is a bacterially derived protein and its behavior in the complex microenvironment of the eukaryotic nucleus is not well understood. Using transgenic human cell lines, I found that gene-silencing heterochromatin impacts Cas9’s ability to bind and cut DNA in a site-specific manner and I investigated ways to improve CRISPR/Cas9 function in heterochromatin.

2. Bacteria use quorum sensing to monitor population density and regulate group behaviors such as virulence, motility, and biofilm formation. Homoserine lactone (HSL) quorum sensing networks are of particular interest to synthetic biologists because they can function as “wires” to connect multiple genetic circuits. However, only four of these networks have been widely implemented in engineered systems. I selected ten quorum sensing networks based on their HSL production profiles and confirmed their functionality in E. coli, significantly expanding the quorum sensing toolset available to synthetic biologists.

Date Created
2017
Contributors
  • Daer, René (Author)
  • Haynes, Karmella (Thesis advisor)
  • Brafman, David (Committee member)
  • Nielsen, David (Committee member)
  • Kiani, Samira (Committee member)
  • Arizona State University (Publisher)
Topical Subject
  • Biology
  • Biomedical Engineering
  • Chromatin
  • CRISPR/Cas9
  • Genome Engineering
  • Quorum Sensing
  • Chromatin
  • Quorum sensing (Microbiology)
Resource Type
Text
Genre
Doctoral Dissertation
Academic theses
Extent
ix, 182 pages : color illustrations
Language
eng
Copyright Statement
In Copyright
Reuse Permissions
All Rights Reserved
Primary Member of
ASU Electronic Theses and Dissertations
Peer-reviewed
No
Open Access
No
Handle
https://hdl.handle.net/2286/R.I.46312
Statement of Responsibility
by Rene Daer
Description Source
Retrieved on June 7, 2018
Level of coding
full
Note
Partial requirement for: Ph.D., Arizona State University, 2017
Note type
thesis
Includes bibliographical references
Note type
bibliography
Field of study: Bioengineering
System Created
  • 2018-02-01 07:09:53
System Modified
  • 2021-08-26 09:47:01
  •     
  • 1 year 5 months ago
Additional Formats
  • OAI Dublin Core
  • MODS XML

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