Peripheral infrastructure vectors and an extended set of plant parts for the Modular Cloning system

PLoS One. 2018 May 30;13(5):e0197185. doi: 10.1371/journal.pone.0197185. eCollection 2018.

Abstract

Standardized DNA assembly strategies facilitate the generation of multigene constructs from collections of building blocks in plant synthetic biology. A common syntax for hierarchical DNA assembly following the Golden Gate principle employing Type IIs restriction endonucleases was recently developed, and underlies the Modular Cloning and GoldenBraid systems. In these systems, transcriptional units and/or multigene constructs are assembled from libraries of standardized building blocks, also referred to as phytobricks, in several hierarchical levels and by iterative Golden Gate reactions. Here, a toolkit containing further modules for the novel DNA assembly standards was developed. Intended for use with Modular Cloning, most modules are also compatible with GoldenBraid. Firstly, a collection of approximately 80 additional phytobricks is provided, comprising e.g. modules for inducible expression systems, promoters or epitope tags. Furthermore, DNA modules were developed for connecting Modular Cloning and Gateway cloning, either for toggling between systems or for standardized Gateway destination vector assembly. Finally, first instances of a "peripheral infrastructure" around Modular Cloning are presented: While available toolkits are designed for the assembly of plant transformation constructs, vectors were created to also use coding sequence-containing phytobricks directly in yeast two hybrid interaction or bacterial infection assays. The presented material will further enhance versatility of hierarchical DNA assembly strategies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agrobacterium tumefaciens / genetics
  • Agrobacterium tumefaciens / metabolism
  • Arabidopsis / genetics
  • Arabidopsis / metabolism
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism
  • Base Sequence
  • Calmodulin / genetics
  • Calmodulin / metabolism
  • Carboxylic Ester Hydrolases / genetics
  • Carboxylic Ester Hydrolases / metabolism
  • Cloning, Molecular / methods*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Gene Expression
  • Genetic Engineering / methods*
  • Genetic Vectors / chemistry*
  • Genetic Vectors / metabolism
  • Nicotiana / genetics*
  • Nicotiana / metabolism
  • Open Reading Frames
  • Plant Leaves / genetics
  • Plant Leaves / metabolism
  • Plant Proteins / genetics*
  • Plant Proteins / metabolism
  • Plants, Genetically Modified
  • Plasmids / chemistry*
  • Plasmids / metabolism
  • Promoter Regions, Genetic
  • Pseudomonas fluorescens / genetics
  • Pseudomonas fluorescens / metabolism
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Two-Hybrid System Techniques
  • Type III Secretion Systems / genetics
  • Type III Secretion Systems / metabolism

Substances

  • Arabidopsis Proteins
  • Calmodulin
  • DNA-Binding Proteins
  • EDS1 protein, Arabidopsis
  • Plant Proteins
  • Recombinant Proteins
  • Type III Secretion Systems
  • Carboxylic Ester Hydrolases
  • PAD4 protein, Arabidopsis

Grants and funding

This work was funded by GRC grant STU 642-1/1 (Deutsche Forschungsgemeinschaft, DFG) and seed funding by the CRC 648 (DFG) to Johannes Stuttmann. Ulla Bonas is acknowledged for generous support. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.