Difference between revisions of "Part:BBa K3600000"
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<partinfo>BBa_K3600000 short</partinfo> | <partinfo>BBa_K3600000 short</partinfo> | ||
− | . | + | HSP12 promoter part plasmid was made in order to create a part plasmid which contains the HSP12 promoter and is compatible with the Yeast Toolkit. |
− | + | To create a promoter part plasmid compatible with the yeast toolkit, at first, we designed a gBlock consisting of the 500bp promoter region, that was retrieved from the yeast genome database, and two linking sequences which were added to the ends of the promoter.These linking sequences contained a BsaI and a BsmBI cutting site each to make Golden Gate assembly possible.Then, the gBlock was inserted into the part plasmid entry vector (pYTK001) through a BsmBI assembly. | |
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===Usage and Biology=== | ===Usage and Biology=== | ||
+ | The HSP12 gene encodes for a heat-shock protein in Saccharomyces Cerevisiae that is activated by the high-osmolarity glycerol (HOG) pathway.<html><a href="#varela1995"><sup>1</sup></a></html> | ||
+ | The HSP12 promoter is regulated by the transcription factor MSN2/4. | ||
+ | Using the yeast toolkit for modular assembly, <html><a href="#Lee2015"><sup>2</sup></a></html> the HSP12 promoter plasmid was used as a part of type II. | ||
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<partinfo>BBa_K3600000 parameters</partinfo> | <partinfo>BBa_K3600000 parameters</partinfo> | ||
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+ | ===Measurements=== | ||
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+ | ===References=== | ||
+ | <HTML><a name=varela1995 style="color:black"> | ||
+ | [1] Varela, J. C., Praekelt, U. M., Meacock, P. A., Planta, R. J. & Mager, W. H. The Saccharomyces cerevisiae HSP12 gene is activated by the high-osmolarity glycerol pathway and negatively regulated by protein kinase A. Molecular and Cellular Biology 15, 6232–6245 (1995). | ||
+ | </a></html> | ||
+ | |||
+ | <HTML><a name=Lee2015 style="color:black"> | ||
+ | [2] Lee, M. E., DeLoache, W. C., Cervantes, B. & Dueber, J. E. A Highly Characterized Yeast Toolkit for Modular, Multipart Assembly. ACS Synth. Biol. 4, 975–986 (2015). | ||
+ | </a></html> | ||
+ | |||
+ | <HTML><a name=Martínez-Pastor1996 style="color:black"> | ||
+ | [3] Martínez-Pastor, M. T. et al. The Saccharomyces cerevisiae zinc finger proteins Msn2p and Msn4p are required for transcriptional induction through the stress response element (STRE). The EMBO Journal 15, 2227–2235 (1996). | ||
+ | </a></html> |
Latest revision as of 18:24, 27 October 2020
HSP12 promoter part plasmid
HSP12 promoter part plasmid was made in order to create a part plasmid which contains the HSP12 promoter and is compatible with the Yeast Toolkit. To create a promoter part plasmid compatible with the yeast toolkit, at first, we designed a gBlock consisting of the 500bp promoter region, that was retrieved from the yeast genome database, and two linking sequences which were added to the ends of the promoter.These linking sequences contained a BsaI and a BsmBI cutting site each to make Golden Gate assembly possible.Then, the gBlock was inserted into the part plasmid entry vector (pYTK001) through a BsmBI assembly.
Usage and Biology
The HSP12 gene encodes for a heat-shock protein in Saccharomyces Cerevisiae that is activated by the high-osmolarity glycerol (HOG) pathway.1 The HSP12 promoter is regulated by the transcription factor MSN2/4. Using the yeast toolkit for modular assembly, 2 the HSP12 promoter plasmid was used as a part of type II.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 308
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 326
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 308
- 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 308
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 57
Illegal BsaI.rc site found at 578