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Team:Valencia UPV/Project/modules/methodology/gb
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| - | <div align="center"><img width=" | + | <div align="center"><img width="650px" src="https://static.igem.org/mediawiki/2014/9/91/VUPV_Gb1.png" alt="solid_phase_extraction" title="Figure 1. Comparison between type II and type IIS restriction enzymes"></img></div><br/> |
<div align="center"><p style="text-align: center; font-size: 0.8em; width: 670px;"><b>Figure 1</b>. Comparison between type II and type IIS restriction enzymes</p></div><br/> | <div align="center"><p style="text-align: center; font-size: 0.8em; width: 670px;"><b>Figure 1</b>. Comparison between type II and type IIS restriction enzymes</p></div><br/> | ||
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| + | <div align="center"><img width="700px" src="https://static.igem.org/mediawiki/2014/f/fc/VUPV_Gb2.png" alt="solid_phase_extraction" title="Figure 2. Part categories of a basic GoldenBraid trancriptional unit. Promoter’s (PROM) prefix is GGAG and its suffix is AATG, which is the same as the coding region’s (CDS) prefix. The same happens with the CDS and the terminator (TER), which share the part identity overhang GCTT, the first one as its suffix and the second one as its prefix."></img></div><br/> | ||
<div align="center"><p style="text-align: center; font-size: 0.8em; width: 670px;"><b>Figure 2</b>. Part categories of a basic GoldenBraid trancriptional unit. Promoter’s (PROM) prefix is GGAG and its suffix is AATG, which is the same as the coding region’s (CDS) prefix. The same happens with the CDS and the terminator (TER), which share the part identity overhang GCTT, the first one as its suffix and the second one as its prefix.</p></div><br/> | <div align="center"><p style="text-align: center; font-size: 0.8em; width: 670px;"><b>Figure 2</b>. Part categories of a basic GoldenBraid trancriptional unit. Promoter’s (PROM) prefix is GGAG and its suffix is AATG, which is the same as the coding region’s (CDS) prefix. The same happens with the CDS and the terminator (TER), which share the part identity overhang GCTT, the first one as its suffix and the second one as its prefix.</p></div><br/> | ||
| + | <p>The mutagenesis procedure required to remove internal restriction sites is standardized and involves the amplification of the target DNA in separated fragments (GBpatches) using GB-adapted primers, which incorporate single mismatches to disrupt the enzyme target sites. Once amplified, GBpatches are reassembled together in a single-tube BsmBI restriction-ligation reaction into the universal entry vector (pUPD) to yield a domesticated GBpart</p> | ||
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| + | <div align="center"><img width="700px" src="https://static.igem.org/mediawiki/2014/9/9a/VUPV_Gb3.png" alt="solid_phase_extraction" title="Figure 3. Domestication strategy with removal of internal restriction sites. Internal Type IIs recognition sites (exemplified here with the GGTCTC BsaI recognition site) are mutagenized during domestication following a standard procedure. In addition to the GB.F and GB.R primers that amplify the whole fragment, two other primers (M.F and M.R) are required for mutagenesis, which incorporate the flanking BsmBI overhangs and the single nucleotide change (C>M). Each primer pair is used to amplify a GBpatch by PCR, and the resulting fragments are assembled together in a BsmBI restriction-ligation reaction into pUPD. The resulting GBpart is free of internal recognition sites and can be released from pUPD using BsaI or BtgZI."></img></div><br/> | ||
| + | <div align="center"><p style="text-align: center; font-size: 0.8em; width: 670px;"><b>Figure 3</b>. Domestication strategy with removal of internal restriction sites. Internal Type IIs recognition sites (exemplified here with the GGTCTC BsaI recognition site) are mutagenized during domestication following a standard procedure. In addition to the GB.F and GB.R primers that amplify the whole fragment, two other primers (M.F and M.R) are required for mutagenesis, which incorporate the flanking BsmBI overhangs and the single nucleotide change (C>M). Each primer pair is used to amplify a GBpatch by PCR, and the resulting fragments are assembled together in a BsmBI restriction-ligation reaction into pUPD. The resulting GBpart is free of internal recognition sites and can be released from pUPD using BsaI or BtgZI.</p></div><br/> | ||
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| + | <p>Domesticated GBparts can now be assembled together in a one-tube-one-step reaction to create a Transcriptional Unit (TU). GB uses the Golden Gate multipartite reaction to create transcriptional units (TU). By using special GB destination vectors in the reaction, we make sure that the resulting TUs can be subsequently used to build multigene constructs (constructs comprising several TUs within the same destination plasmid). GB destination vectors are T-plasmids, a special type of plasmids used for plant transformation. Therefore the new TUs assembled in GB vectors can be directly transferred into plants using Agrobacterium-mediated plant transformation.</p> | ||
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Revision as of 00:17, 18 October 2014
Project > Modules > Methodology > Cloning > GolgenBraid
Our Sexy Plant is a challenging project for many reasons; a very important one is that we use plants as chassis for engineering. Plants have eukaryotic gene structure, make use of plant-specific regulatory regions and require special T-vectors for transformation, among other special features. Consequently, DNA repositories and DNA assembly standards need certain adaptations to facilitate engineering using plant chassis. Without letting aside BioBricks, we decided to use the GoldenBraid system (GB) to build several of the intermediate genetic constructs employed in this project. GB is a DNA assembly system specially conceived to facilitate genetic engineering in Plant Synthetic Biology projects (visit gbcloning.org for more information).
As BioBricks, GB is a modular cloning strategy that allows the fabrication of new devices by the combination of prefabricated standard modules. A difference between both strategies is that BioBricks is based on type II enzymes and GB relies on the use of type IIS restriction enzymes.
Type IIS restriction enzymes, unlike type II enzymes; cleave DNA at a defined distance from their recognition sites, not requiring any specific sequence in the cleavage site. Since there are no sequence requirements in the cleavage sites, these can be defined by the user and adapted to serve as standard fusion sites to DNA parts. The enzymes used in GoldenBraid are BsaI and BsmBI, which cut out from their binding sites generating 4 base overhangs.
Figure 1. Comparison between type II and type IIS restriction enzymes
GoldenBraid step by step
1. GB Domestication
The first step in the GB cloning strategy is the adaptation of the DNA sequence to the GB standard. This process is called domestication and implies (1) the removal of internal restriction sites for the enzymes used in GB (BsaI, BsmBI and BtgZI) and (2) the addition of appropriate 4-nt flanking overhangs to convert the DNA sequence into a standard part (Gbpart). Gbparts are the minimal standard building blocks and they are classified in different categories according to their specific function.
Figure 2. Part categories of a basic GoldenBraid trancriptional unit. Promoter’s (PROM) prefix is GGAG and its suffix is AATG, which is the same as the coding region’s (CDS) prefix. The same happens with the CDS and the terminator (TER), which share the part identity overhang GCTT, the first one as its suffix and the second one as its prefix.
The mutagenesis procedure required to remove internal restriction sites is standardized and involves the amplification of the target DNA in separated fragments (GBpatches) using GB-adapted primers, which incorporate single mismatches to disrupt the enzyme target sites. Once amplified, GBpatches are reassembled together in a single-tube BsmBI restriction-ligation reaction into the universal entry vector (pUPD) to yield a domesticated GBpart
Figure 3. Domestication strategy with removal of internal restriction sites. Internal Type IIs recognition sites (exemplified here with the GGTCTC BsaI recognition site) are mutagenized during domestication following a standard procedure. In addition to the GB.F and GB.R primers that amplify the whole fragment, two other primers (M.F and M.R) are required for mutagenesis, which incorporate the flanking BsmBI overhangs and the single nucleotide change (C>M). Each primer pair is used to amplify a GBpatch by PCR, and the resulting fragments are assembled together in a BsmBI restriction-ligation reaction into pUPD. The resulting GBpart is free of internal recognition sites and can be released from pUPD using BsaI or BtgZI.
Domesticated GBparts can now be assembled together in a one-tube-one-step reaction to create a Transcriptional Unit (TU). GB uses the Golden Gate multipartite reaction to create transcriptional units (TU). By using special GB destination vectors in the reaction, we make sure that the resulting TUs can be subsequently used to build multigene constructs (constructs comprising several TUs within the same destination plasmid). GB destination vectors are T-plasmids, a special type of plasmids used for plant transformation. Therefore the new TUs assembled in GB vectors can be directly transferred into plants using Agrobacterium-mediated plant transformation.
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