iBrick: A New Standard for Iterative Assembly of Biological Parts with Homing Endonucleases

The BioBricks standard has made the construction of DNA modules easier, quicker and cheaper. So far, over 100 BioBricks assembly schemes have been developed and many of them, including the original standard of BBF RFC 10, are now widely used. However, because the restriction endonucleases employed by these standards usually recognize short DNA sequences that are widely spread among natural DNA sequences, and these recognition sites must be removed before the parts construction, there is much inconvenience in dealing with large-size DNA parts (e.g., more than couple kilobases in length) with the present standards. Here, we introduce a new standard, namely iBrick, which uses two homing endonucleases of I-SceI and PI-PspI. Because both enzymes recognize long DNA sequences (>18 bps), their sites are extremely rare in natural DNA sources, thus providing additional convenience, especially in handling large pieces of DNA fragments. Using the iBrick standard, the carotenoid biosynthetic cluster (>4 kb) was successfully assembled and the actinorhodin biosynthetic cluster (>20 kb) was easily cloned and heterologously expressed. In addition, a corresponding nomenclature system has been established for the iBrick standard.

[1]  A. Komar,et al.  Silent SNPs: impact on gene function and phenotype. , 2007, Pharmacogenomics.

[2]  William J. Blake,et al.  Creation of a type IIS restriction endonuclease with a long recognition sequence , 2009, Nucleic acids research.

[3]  A. Komar Genetics. SNPs, silent but not invisible. , 2007, Science.

[4]  Jean Peccoud,et al.  Building block synthesis using the polymerase chain assembly method. , 2012, Methods in molecular biology.

[5]  B. Dujon,et al.  Recognition and cleavage site of the intron-encoded omega transposase. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[6]  D. Endy Foundations for engineering biology , 2005, Nature.

[7]  Sylvestre Marillonnet,et al.  Generation of families of construct variants using golden gate shuffling. , 2011, Methods in molecular biology.

[8]  B. Dujon,et al.  Site-specific recombination determined by I-SceI, a mitochondrial group I intron-encoded endonuclease expressed in the yeast nucleus. , 1992, Genetics.

[9]  A. Glieder,et al.  Deletion of the Pichia pastoris KU70 Homologue Facilitates Platform Strain Generation for Gene Expression and Synthetic Biology , 2012, PloS one.

[10]  B. Dujon,et al.  Purification and characterization of the in vitro activity of I-Sce I, a novel and highly specific endonuclease encoded by a group I intron. , 1990, Nucleic acids research.

[11]  Lu Wang,et al.  DNA cleavage is independent of synapsis during Streptomyces phage phiBT1 integrase-mediated site-specific recombination. , 2010, Journal of molecular cell biology.

[12]  C. Yanisch-Perron,et al.  Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. , 1985, Gene.

[13]  P. M. Booth,et al.  Assembly and cloning of coding sequences for neurotrophic factors directly from genomic DNA using polymerase chain reaction and uracil DNA glycosylase. , 1994, Gene.

[14]  D. Kobayashi,et al.  Improved broad-host-range plasmids for DNA cloning in gram-negative bacteria. , 1988, Gene.

[15]  T. Kieser Practical streptomyces genetics , 2000 .

[16]  Ryan Hunt,et al.  Silent (synonymous) SNPs: should we care about them? , 2009, Methods in molecular biology.

[17]  K. Chater,et al.  Lambda red-mediated genetic manipulation of antibiotic-producing Streptomyces. , 2004, Advances in applied microbiology.

[18]  Viret Jf Meganuclease I-SceI as a tool for the easy subcloning of large DNA fragments devoid of selection marker. , 1993 .

[19]  Guoping Zhao,et al.  Tandem assembly of the epothilone biosynthetic gene cluster by in vitro site-specific recombination , 2011, Scientific reports.

[20]  W. Szybalski,et al.  Conditionally amplifiable BACs: switching from single-copy to high-copy vectors and genomic clones. , 2002, Genome research.

[21]  Fumio Arisaka,et al.  Bacteriophage T4 Genome , 2003, Microbiology and Molecular Biology Reviews.

[22]  J. LaBaer,et al.  Many paths to many clones: a comparative look at high-throughput cloning methods. , 2004, Genome research.

[23]  K. O'Brien,et al.  Plasmid cloning vectors for the conjugal transfer of DNA from Escherichia coli to Streptomyces spp. , 1992, Gene.

[24]  W. Stemmer,et al.  Single-step assembly of a gene and entire plasmid from large numbers of oligodeoxyribonucleotides. , 1995, Gene.

[25]  T. Mamedov,et al.  Rational de novo gene synthesis by rapid polymerase chain assembly (PCA) and expression of endothelial protein-C and thrombin receptor genes. , 2007, Journal of biotechnology.

[26]  J. Pronk,et al.  One-step assembly and targeted integration of multigene constructs assisted by the I-SceI meganuclease in Saccharomyces cerevisiae , 2013, FEMS yeast research.

[27]  J Craig Venter,et al.  Chemical synthesis of the mouse mitochondrial genome , 2010, Nature Methods.

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

[29]  A. Burkovski,et al.  Nitrogen Control in Mycobacterium smegmatis: Nitrogen-Dependent Expression of Ammonium Transport and Assimilation Proteins Depends on the OmpR-Type Regulator GlnR , 2008, Journal of bacteriology.

[30]  Z. Qin,et al.  Development of a gene cloning system in a fast-growing and moderately thermophilic Streptomyces species and heterologous expression of Streptomyces antibiotic biosynthetic gene clusters , 2011, BMC Microbiology.

[31]  Brad A. Chapman,et al.  Pairwise selection assembly for sequence-independent construction of long-length DNA , 2010, Nucleic acids research.

[32]  James J. Collins,et al.  Next-Generation Synthetic Gene Networks , 2009, Nature Biotechnology.

[33]  Carola Engler,et al.  Golden Gate Shuffling: A One-Pot DNA Shuffling Method Based on Type IIs Restriction Enzymes , 2009, PloS one.

[34]  Meghdad Hajimorad,et al.  BglBrick vectors and datasheets: A synthetic biology platform for gene expression , 2011, Journal of biological engineering.

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

[36]  Elsje Pienaar,et al.  Gene synthesis by integrated polymerase chain assembly and PCR amplification using a high-speed thermocycler. , 2009, Journal of microbiological methods.

[37]  Wei-Hua Chen,et al.  The MASTER (methylation-assisted tailorable ends rational) ligation method for seamless DNA assembly , 2013, Nucleic acids research.

[38]  B. Wanner,et al.  One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[39]  M. Nefedov,et al.  Targeted modification of a human beta-globin locus BAC clone using GET Recombination and an I-Scei counterselection cassette. , 2003, Genomics.

[40]  N. Kouprina,et al.  TAR cloning: insights into gene function, long-range haplotypes and genome structure and evolution , 2006, Nature Reviews Genetics.

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

[42]  A. Komar SNPs, Silent But Not Invisible , 2007, Science.

[43]  Gunvor Røkke,et al.  BioBrick assembly standards and techniques and associated software tools. , 2014, Methods in molecular biology.

[44]  Thomas H Segall-Shapiro,et al.  Creation of a Bacterial Cell Controlled by a Chemically Synthesized Genome , 2010, Science.

[45]  Rolf Müller,et al.  Full-length RecE enhances linear-linear homologous recombination and facilitates direct cloning for bioprospecting , 2012, Nature Biotechnology.

[46]  Francine B. Perler,et al.  In vitro protein splicing of purified precursor and the identification of a branched intermediate , 1993, Cell.