Difference between revisions of "Part:BBa K909009"
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<partinfo>BBa_K909009 short</partinfo> | <partinfo>BBa_K909009 short</partinfo> | ||
− | [[Image:UVR8_2.png|frameless| | + | [[Image:UVR8_2.png|frameless|200px|right|thumb| UVR8 as a symmetric homodimer. Upon UV-B exposure the the dimer dissociates into two monomers. [http://www.cell.com/trends/plant-science/abstract/S1360-1385%2812%2900008-8 (Heijde 2012)] |
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UVR8 (UV resistance locus 8) is UV-B photoreceptor found in plants as a crucial mediator of plants response to UV-B response. In absence of UV-B the protein occurs as a dimer, which breaks upon UV-B irradiation. | UVR8 (UV resistance locus 8) is UV-B photoreceptor found in plants as a crucial mediator of plants response to UV-B response. In absence of UV-B the protein occurs as a dimer, which breaks upon UV-B irradiation. | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
− | Differently from other photoreceptors, UVR8 uses tryptophane residues present in the structure, rather than external chromophores. Energy from UV-B light is absorbed by these triptophanes at the dimer interface is later used to break dimer cross-salt bridges resulting in the dissociation of the UVR8 monomers [Christie 2012]. Monomeric UVR8 is then able to initiate downstream reactions that trigger the transcription of proteins needed for the UV-B caused stress response [Heijde 2012]. | + | Differently from other photoreceptors, UVR8 uses tryptophane residues present in the structure, rather than external chromophores. Energy from UV-B light is absorbed by these triptophanes at the dimer interface is later used to break dimer cross-salt bridges resulting in the dissociation of the UVR8 monomers [http://www.sciencemag.org/content/335/6075/1492.long (Christie 2012)]. Monomeric UVR8 is then able to initiate downstream reactions that trigger the transcription of proteins needed for the UV-B caused stress response [http://www.cell.com/trends/plant-science/abstract/S1360-1385%2812%2900008-8 (Heijde 2012)]. |
In addition a BamHI site is inserted after ATG codon for fusions with other proteins (e.g. tetR-DNA binding domain (<partinfo>BBa_K909007</partinfo>)), to use UVR8 as a UV-B sensing domain (<partinfo>BBa_K909008</partinfo>). | In addition a BamHI site is inserted after ATG codon for fusions with other proteins (e.g. tetR-DNA binding domain (<partinfo>BBa_K909007</partinfo>)), to use UVR8 as a UV-B sensing domain (<partinfo>BBa_K909008</partinfo>). |
Revision as of 23:44, 26 September 2012
cDNA of UV-B sensing protein UVR8 from Arabidopsis thaliana
UVR8 (UV resistance locus 8) is UV-B photoreceptor found in plants as a crucial mediator of plants response to UV-B response. In absence of UV-B the protein occurs as a dimer, which breaks upon UV-B irradiation.
Usage and Biology
Differently from other photoreceptors, UVR8 uses tryptophane residues present in the structure, rather than external chromophores. Energy from UV-B light is absorbed by these triptophanes at the dimer interface is later used to break dimer cross-salt bridges resulting in the dissociation of the UVR8 monomers [http://www.sciencemag.org/content/335/6075/1492.long (Christie 2012)]. Monomeric UVR8 is then able to initiate downstream reactions that trigger the transcription of proteins needed for the UV-B caused stress response [http://www.cell.com/trends/plant-science/abstract/S1360-1385%2812%2900008-8 (Heijde 2012)].
In addition a BamHI site is inserted after ATG codon for fusions with other proteins (e.g. tetR-DNA binding domain (BBa_K909007)), to use UVR8 as a UV-B sensing domain (BBa_K909008).
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 560
Illegal PstI site found at 1214 - 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 76
Illegal PstI site found at 560
Illegal PstI site found at 1214 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 4
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 560
Illegal PstI site found at 1214 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 560
Illegal PstI site found at 1214 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 91