A unified multi-kingdom Golden Gate cloning platform

Show simple item record

dc.creator Chiasson, David
dc.creator Giménez-Oya, Victor
dc.creator Bircheneder, Martin
dc.creator Bachmaier, Sabine
dc.creator Studtrucker, Tanja
dc.creator Ryan, Joel
dc.creator Sollweck, Katharina
dc.creator Leonhardt, Heinrich
dc.creator Boshart, Michael
dc.creator Dietrich, Petra
dc.creator Parniske, Martin
dc.date.accessioned 2022-05-02T16:51:52Z
dc.date.available 2022-05-02T16:51:52Z
dc.date.issued 2019-07-12
dc.identifier.issn 2045-2322
dc.identifier.uri http://library2.smu.ca/xmlui/handle/01/30903
dc.description Published version en_CA
dc.description.abstract Assembling composite DNA modules from custom DNA parts has become routine due to recent technological breakthroughs such as Golden Gate modular cloning. Using Golden Gate, one can efficiently assemble custom transcription units and piece units together to generate higher-order assemblies. Although Golden Gate cloning systems have been developed to assemble DNA plasmids required for experimental work in model species, they are not typically applicable to organisms from other kingdoms. Consequently, a typical molecular biology laboratory working across kingdoms must use multiple cloning strategies to assemble DNA constructs for experimental assays. To simplify the DNA assembly process, we developed a multi-kingdom (MK) Golden Gate assembly platform for experimental work in species from the kingdoms Fungi, Eubacteria, Protista, Plantae, and Animalia. Plasmid backbone and part overhangs are consistent across the platform, saving both time and resources in the laboratory. We demonstrate the functionality of the system by performing a variety of experiments across kingdoms including genome editing, fluorescence microscopy, and protein interaction assays. The versatile MK system therefore streamlines the assembly of modular DNA constructs for biological assays across a range of model organisms. en_CA
dc.description.provenance Submitted by Sherry Briere (sherry.briere@smu.ca) on 2022-05-02T16:51:52Z No. of bitstreams: 1 Chiasson_David_article_2019.pdf: 2927590 bytes, checksum: 0fbf6c6a04ab9a62b9b7e823d2fd7c73 (MD5) en
dc.description.provenance Made available in DSpace on 2022-05-02T16:51:52Z (GMT). No. of bitstreams: 1 Chiasson_David_article_2019.pdf: 2927590 bytes, checksum: 0fbf6c6a04ab9a62b9b7e823d2fd7c73 (MD5) Previous issue date: 2019-07-12 en
dc.language.iso en_CA en_CA
dc.publisher Springer Nature en_CA
dc.relation.uri https://doi.org/10.1038/s41598-019-46171-2
dc.rights © The Author(s) 2019. <a rel="license" href="http://creativecommons.org/licenses/by/4.0/"><img alt="Creative Commons License" style="border-width:0" src="https://i.creativecommons.org/l/by/4.0/80x15.png" /></a> This work is licensed under a <a rel="license" href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution 4.0 International License</a>
dc.subject.lcsh Molecular cloning -- Methods
dc.subject.lcsh Genetic transcription
dc.subject.lcsh DNA
dc.subject.lcsh Molecular biology
dc.subject.lcsh Gene editing
dc.subject.lcsh Fluorescence microscopy
dc.subject.lcsh Protein-protein interactions
dc.title A unified multi-kingdom Golden Gate cloning platform en_CA
dc.type Text en_CA
dcterms.bibliographicCitation Scientific Reports 9(1): 10131. (2019) en_CA
 Find Full text

Files in this item


 

Copyright statement:

 
© The Author(s) 2019. Creative Commons License This work is licensed under a Creative Commons Attribution 4.0 International License
 
Published Version: https://doi.org/10.1038/s41598-019-46171-2
 
 

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Browse

My Account