Difference between revisions of "Part:BBa K626005"

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This composite artificial transcription factor will activate any reporter or any gene in general that has a UAS (Upper Activating Sequence) 3' of it's promoter. The usual binding sites of reporters, contain multiple UAS elements. In order to have a POPS output, the LBD has to recruit activators in the cell. This can be initiated by ligand binding or by recruiting a protein that has a fused strong activator like the VP activator.
 
This composite artificial transcription factor will activate any reporter or any gene in general that has a UAS (Upper Activating Sequence) 3' of it's promoter. The usual binding sites of reporters, contain multiple UAS elements. In order to have a POPS output, the LBD has to recruit activators in the cell. This can be initiated by ligand binding or by recruiting a protein that has a fused strong activator like the VP activator.
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More on GAL4 DNA binding domain: [http://en.wikipedia.org/wiki/Two-hybrid_screening].
 +
 +
Uniprot GAL4 DNA binding domain: [http://www.uniprot.org/uniprot/P04386].
 +
 +
View GAL4 DNA binding domain crystal structure here: [http://www.rcsb.org/pdb/explore/jmol.do?structureId=3COQ&bionumber=1].
  
 
With this system NHR (Nuclear Hormone Receptor) ligands or NHR interacting partners can be screened.
 
With this system NHR (Nuclear Hormone Receptor) ligands or NHR interacting partners can be screened.

Revision as of 21:13, 19 September 2011

Gal4 - NHR64

This composite part is a nuclear hormone receptor consisting of a Gal4 yeast transcription factor and NHR64 (C. elegans Nuclear Hormone Receptor 64) Ligand Binding domain. This part can be used as a transcription factor regulated by unknown lipid molecules for the regulation of genes having UAS before their protein coding sequence.

NHR 64 LBD

The nhr-64 encodes a conserved nuclear receptor that is a member of the NR2 subfamily of nuclear receptors that contains Drosophila and human HNF4 (mutations in human HNF4A are associated with Type I MODY (maturity-onset diabetes of the young)). By homology, NHR-64 is predicted to function as a transcription factor that may activate or repress transcription in response to a hormonal signal. However, as loss of nhr-64 activity via RNAi does not result in any obvious abnormalities, the precise role of NHR-64 in C. elegans development and/or behavior is not yet known. The nhr-64 is broadly expressed and detected in anterior and posterior neurons, the ventral nerve cord, the pharynx, gut, and hypodermis.

Gal4 DBD

This protein is a positive regulator for the gene expression of the galactose-induced genes such as GAL1, GAL2, GAL7, GAL10, and MEL1 which encode for the enzymes used to convert galactose to glucose. This protein contains a fungal Zn(2)-Cys(6) binuclear cluster domain.

This composite artificial transcription factor will activate any reporter or any gene in general that has a UAS (Upper Activating Sequence) 3' of it's promoter. The usual binding sites of reporters, contain multiple UAS elements. In order to have a POPS output, the LBD has to recruit activators in the cell. This can be initiated by ligand binding or by recruiting a protein that has a fused strong activator like the VP activator.

More on GAL4 DNA binding domain: [http://en.wikipedia.org/wiki/Two-hybrid_screening].

Uniprot GAL4 DNA binding domain: [http://www.uniprot.org/uniprot/P04386].

View GAL4 DNA binding domain crystal structure here: [http://www.rcsb.org/pdb/explore/jmol.do?structureId=3COQ&bionumber=1].

With this system NHR (Nuclear Hormone Receptor) ligands or NHR interacting partners can be screened.

The NHR: cofactor-VP interaction should be also broken by a potential ligand binding, this is why this setup is also suitable for ligand identification. The benefit of the cofactor-VP interaction test is that the dynamic range of the assay is much higher than the dynamic range of the normal Gal4-NHR ligand activation assay.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 218
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 137
    Illegal BsaI.rc site found at 627