Universal loop assembly: open, efficient and cross-kingdom DNA fabrication

Abstract Standardized type IIS DNA assembly methods are becoming essential for biological engineering and research. These methods are becoming widespread and more accessible due to the proposition of a ‘common syntax’ that enables higher interoperability between DNA libraries. Currently, Golden Gate (GG)-based assembly systems, originally implemented in host-specific vectors, are being made compatible with multiple organisms. We have recently developed the GG-based Loop assembly system for plants, which uses a small library and an intuitive strategy for hierarchical fabrication of large DNA constructs (>30 kb). Here, we describe ‘universal Loop’ (uLoop) assembly, a system based on Loop assembly for use in potentially any organism of choice. This design permits the use of a compact number of plasmids (two sets of four odd and even vectors), which are utilized repeatedly in alternating steps. The elements required for transformation/maintenance in target organisms are also assembled as standardized parts, enabling customization of host-specific plasmids. Decoupling of the Loop assembly logic from the host-specific propagation elements enables universal DNA assembly that retains high efficiency regardless of the final host. As a proof-of-concept, we show the engineering of multigene expression vectors in diatoms, yeast, plants and bacteria. These resources are available through the OpenMTA for unrestricted sharing and open access.

[1]  William C. Deloache,et al.  A Highly Characterized Yeast Toolkit for Modular, Multipart Assembly. , 2015, ACS synthetic biology.

[2]  J. Sheen,et al.  Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis , 2007, Nature Protocols.

[3]  N. Nakayama,et al.  Mobius Assembly: A versatile Golden-Gate framework towards universal DNA assembly , 2018, PloS one.

[4]  A. Grossman,et al.  In vivo characterization of diatom multipartite plastid targeting signals , 2002, Journal of Cell Science.

[5]  Pamela A. Silver,et al.  Rapid construction of insulated genetic circuits via synthetic sequence-guided isothermal assembly , 2013, Nucleic acids research.

[6]  Fabien Burki The eukaryotic tree of life from a global phylogenomic perspective. , 2014, Cold Spring Harbor perspectives in biology.

[7]  Olaf Kruse,et al.  Birth of a Photosynthetic Chassis: A MoClo Toolkit Enabling Synthetic Biology in the Microalga Chlamydomonas reinhardtii. , 2018, ACS synthetic biology.

[8]  D. G. Gibson,et al.  Enzymatic assembly of DNA molecules up to several hundred kilobases , 2009, Nature Methods.

[9]  Herbert M Sauro,et al.  Visualization of evolutionary stability dynamics and competitive fitness of Escherichia coli engineered with randomized multigene circuits. , 2013, ACS synthetic biology.

[10]  Drew Endy,et al.  Engineering BioBrick vectors from BioBrick parts , 2008, Journal of Biological Engineering.

[11]  R. Schiestl,et al.  Large-scale high-efficiency yeast transformation using the LiAc/SS carrier DNA/PEG method , 2007, Nature Protocols.

[12]  Christopher A. Voigt,et al.  Genetic circuit design automation , 2016, Science.

[13]  L. Nielsen,et al.  Knock-in/Knock-out (KIKO) vectors for rapid integration of large DNA sequences, including whole metabolic pathways, onto the Escherichia coli chromosome at well-characterised loci , 2013, Microbial Cell Factories.

[14]  R. D. Gietz,et al.  Yeast transformation by the LiAc/SS carrier DNA/PEG method. , 2014, Methods in molecular biology.

[15]  Heinrich Leonhardt,et al.  A unified multi-kingdom Golden Gate cloning platform , 2019, Scientific Reports.

[16]  J. Kudla,et al.  A ubiquitin-10 promoter-based vector set for fluorescent protein tagging facilitates temporal stability and native protein distribution in transient and stable expression studies. , 2010, The Plant journal : for cell and molecular biology.

[17]  Christopher E. French,et al.  Joint Universal Modular Plasmids (JUMP): A flexible and comprehensive platform for synthetic biology , 2019, bioRxiv.

[18]  Jacob Beal,et al.  CIDAR MoClo: Improved MoClo Assembly Standard and New E. coli Part Library Enable Rapid Combinatorial Design for Synthetic and Traditional Biology. , 2016, ACS synthetic biology.

[19]  Ruben E. Valas,et al.  Designer diatom episomes delivered by bacterial conjugation , 2015, Nature Communications.

[20]  A. Johns,et al.  Provenance and risk in transfer of biological materials , 2018, PLoS biology.

[21]  A. Falciatore,et al.  Gene silencing in the marine diatom Phaeodactylum tricornutum , 2009, Nucleic acids research.

[22]  Ansgar Gruber,et al.  Rapid induction of GFP expression by the nitrate reductase promoter in the diatom Phaeodactylum tricornutum , 2016, PeerJ.

[23]  Drew Endy,et al.  Opening options for material transfer , 2018, Nature Biotechnology.

[24]  Christian Rogers,et al.  Standards for plant synthetic biology: a common syntax for exchange of DNA parts. , 2015, The New phytologist.

[25]  Huimin Zhao,et al.  Recent advances in DNA assembly technologies. , 2014, FEMS yeast research.

[26]  R. Waller,et al.  Strength in numbers: Collaborative science for new experimental model systems , 2018, bioRxiv.

[27]  Svein Valla,et al.  A New and Improved Host-Independent Plasmid System for RK2-Based Conjugal Transfer , 2014, PloS one.

[28]  Hana El-Samad,et al.  A Toolkit for Rapid Modular Construction of Biological Circuits in Mammalian Cells , 2018, bioRxiv.

[29]  Sylvestre Marillonnet,et al.  Fast track assembly of multigene constructs using Golden Gate cloning and the MoClo system. , 2012, Bioengineered bugs.

[30]  Nicola J. Patron,et al.  A golden gate modular cloning toolbox for plants. , 2014, ACS synthetic biology.

[31]  T. Ellis,et al.  Bricks and blueprints: methods and standards for DNA assembly , 2015, Nature Reviews Molecular Cell Biology.

[32]  A. Granell,et al.  GoldenBraid: An Iterative Cloning System for Standardized Assembly of Reusable Genetic Modules , 2011, PloS one.

[33]  Da Lin,et al.  MetClo: methylase-assisted hierarchical DNA assembly using a single type IIS restriction enzyme , 2018, Nucleic acids research.

[34]  Anthony West,et al.  Loop Assembly: a simple and open system for recursive fabrication of DNA circuits , 2018, bioRxiv.

[35]  Ernst Weber,et al.  A Modular Cloning System for Standardized Assembly of Multigene Constructs , 2011, PloS one.

[36]  G. Piétu,et al.  Effect of plasmid size on transformation efficiency by electroporation of Escherichia coli DH5 alpha. , 1994, BioTechniques.

[37]  Carola Engler,et al.  A One Pot, One Step, Precision Cloning Method with High Throughput Capability , 2008, PloS one.

[38]  U. Maier,et al.  A Single Peroxisomal Targeting Signal Mediates Matrix Protein Import in Diatoms , 2011, PloS one.

[39]  A. Allen,et al.  Refinement of the Diatom Episome Maintenance Sequence and Improvement of Conjugation-Based DNA Delivery Methods , 2016, Front. Bioeng. Biotechnol..

[40]  Tom Ellis,et al.  DNA assembly for synthetic biology: from parts to pathways and beyond. , 2011, Integrative biology : quantitative biosciences from nano to macro.

[41]  S. Cutler,et al.  Random GFP::cDNA fusions enable visualization of subcellular structures in cells of Arabidopsis at a high frequency. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[42]  Andrew D. Halleran,et al.  Single day construction of multi-gene circuits with 3G assembly , 2018, bioRxiv.