Difference between revisions of "Part:BBa K2549038"
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<partinfo>BBa_K2549038 short</partinfo> | <partinfo>BBa_K2549038 short</partinfo> | ||
− | This part is one of the downstream elements of our amplifier. It is constructed by fusing CfaC, ZF21.16C and NLS, from N terminal to C terminal. CfaC is the C-terminal fragment of Cfa which is a consensus sequence from an alignment of 73 naturally occurring DnaE inteins that are predicted to have fast splicing rates. ZF21.16C is the C-terminal fragment of the zinc finger whose recognition helices for three-finger arrays are substituted by the reported synthetic zinc finger 21.16 residues on the basis of the BCR_ABL-1 artificial zinc finger. NLS is a short nuclear location sequence from SV40 large T antigen. When coexpressed with VP64-ZF21.16N-CfaN in the same cell, both fusions are formed and a transcription activating function is executed. | + | This part is one of the downstream elements of our amplifier. It is constructed by fusing CfaC ([[Part:BBa_K2549010]]), ZF21.16C ([[Part:BBa_K2549012]]) and NLS ([[Part:BBa_K2549054]]), from N terminal to C terminal. CfaC is the C-terminal fragment of Cfa which is a consensus sequence from an alignment of 73 naturally occurring DnaE inteins that are predicted to have fast splicing rates. ZF21.16C is the C-terminal fragment of the zinc finger whose recognition helices for three-finger arrays are substituted by the reported synthetic zinc finger 21.16 residues on the basis of the BCR_ABL-1 artificial zinc finger<ref>A tunable zinc finger-based framework for Boolean logic computation in mammalian cells. Lohmueller JJ, Armel TZ, Silver PA. Nucleic Acids Res, 2012 Jun;40(11):5180-7 PMID: 22323524; DOI: 10.1093/nar/gks142</ref>. NLS is a short nuclear location sequence from SV40 large T antigen. When coexpressed with VP64-ZF21.16N-CfaN ([[Part:BBa_K2549036]]) in the same cell, both fusions are formed and a transcription activating function is executed. Also, when coexpressed with KRAB-ZF21.16N-CfaN ([[Part:BBa_K2549037]]) in the same cell, both fusions are formed and a transcription repressing function is executed. |
− | <!-- Add more about the biology of this part here | + | <!-- Add more about the biology of this part here --> |
− | === | + | ===Biology=== |
+ | ====Boolean logic gates via split zinc finger-based transcription factors==== | ||
+ | Lohmueller JJ et al have demonstrated the split ZF-TF reconstitution process. | ||
+ | |||
+ | [[File:ZF-TF.jpg|none|400px|thumb|Lohmueller JJ et al demonstrated:''After expression, the two split ZF-intein fragments bind together and undergo protein splicing to cleave away intein fragments and reconstitute the full ZF activator leading to activation of the BCR_ABL reporter.'']] | ||
+ | |||
+ | [[File:zfAND.jpg|none|400px|thumb|Lohmueller JJ et al demonstrated:''For AND gates, a ZF activator is spliced and the logical operation is computed as TRUE only when both input signals are present. For the response data shown BCR_ABL-1:GCN4 activator split fragments were used and the response promoter contains 6 copies of the BCR_ABL target site. CFP expression was measured by flow cytometry and expressed as fold change over an off-target expression control.'']] | ||
+ | |||
+ | [[File:zfNAND.jpeg|none|400px|thumb|Lohmueller JJ et al demonstrated:''For NAND gates, the computational module splices a ZF repressor, and the logical operation is computed as TRUE as long as both inputs are not present together. For the response data shown BCR_ABL-1:GCN4 repressor split fragments were used and the response promoter contains 6 copies of the BCR_ABL target site. CFP expression was measured by flow cytometry and expressed as fold change over an off-target expression control.'']] | ||
+ | |||
+ | ===coexpressed with VP64-ZF21.16N-CfaN or KRAB-ZF21.16N-CfaN in the same cell=== | ||
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+ | ===References=== |
Revision as of 03:29, 11 October 2018
CfaC-ZF21.16C-NLS
This part is one of the downstream elements of our amplifier. It is constructed by fusing CfaC (Part:BBa_K2549010), ZF21.16C (Part:BBa_K2549012) and NLS (Part:BBa_K2549054), from N terminal to C terminal. CfaC is the C-terminal fragment of Cfa which is a consensus sequence from an alignment of 73 naturally occurring DnaE inteins that are predicted to have fast splicing rates. ZF21.16C is the C-terminal fragment of the zinc finger whose recognition helices for three-finger arrays are substituted by the reported synthetic zinc finger 21.16 residues on the basis of the BCR_ABL-1 artificial zinc finger[1]. NLS is a short nuclear location sequence from SV40 large T antigen. When coexpressed with VP64-ZF21.16N-CfaN (Part:BBa_K2549036) in the same cell, both fusions are formed and a transcription activating function is executed. Also, when coexpressed with KRAB-ZF21.16N-CfaN (Part:BBa_K2549037) in the same cell, both fusions are formed and a transcription repressing function is executed.
Biology
Boolean logic gates via split zinc finger-based transcription factors
Lohmueller JJ et al have demonstrated the split ZF-TF reconstitution process.
coexpressed with VP64-ZF21.16N-CfaN or KRAB-ZF21.16N-CfaN in the same cell
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 91
Illegal SapI.rc site found at 21
References
- ↑ A tunable zinc finger-based framework for Boolean logic computation in mammalian cells. Lohmueller JJ, Armel TZ, Silver PA. Nucleic Acids Res, 2012 Jun;40(11):5180-7 PMID: 22323524; DOI: 10.1093/nar/gks142