Difference between revisions of "Part:BBa K1907004"
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The functionality of this promoter has been tested in association with the Venus YFP reporter in <i>S. cerevisiae </i> strain SS328-leu, and proven to be functional when oxidative stress is induced by hydrogen peroxide. The TSA1 promoter has a relatively high base level of expression, but expression levels are further driven up when induced.</p> | The functionality of this promoter has been tested in association with the Venus YFP reporter in <i>S. cerevisiae </i> strain SS328-leu, and proven to be functional when oxidative stress is induced by hydrogen peroxide. The TSA1 promoter has a relatively high base level of expression, but expression levels are further driven up when induced.</p> | ||
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+ | <span class='h3bb'><p><b>Sequence and Features</b></p><p> | ||
+ | <partinfo>BBa_K1907005 SequenceAndFeatures</partinfo> | ||
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+ | <b>References</b></p><p> | ||
+ | He, X.J. and Fassler, J.S., 2005. Identification of novel Yap1p and Skn7p binding sites involved in the oxidative stress response of Saccharomyces cerevisiae. Molecular microbiology, 58(5), pp.1454-1467. | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
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Revision as of 18:36, 19 October 2016
TSA1 promoter for S. cerevisiae
Introduction
TSA1 is a gene for thioredoxin peroxidase - a protein that acts as both a ribosome-associated and a free cytoplasmic antioxidant. It self-associates to form a high-molecular weight chaperone complex under oxidative stress. As Tsa1p is produced under oxidative stress, its promoter is activated in these conditions. (Saccharomyces genome database ID: S000004490)
This part contains a promoter region (260 bp) of TSA1 gene. The length of promoter region is chosen so that it contains identified Skn7 and Yap1 binding sites and doesn’t overlap with the next gene in the genome. (He et al., 2005; SGD ID:S000004490) Skn7 and Yap1 are the main transcription factors activated in oxidative stress and are thus responsible for TSA1 promoter activation. The gene sequence for the TSA1 promoter region is taken from strain S288C of Saccharomyces cerevisiae, obtained from the Saccharomyces Genome Database.
The functionality of this promoter has been tested in association with the Venus YFP reporter in S. cerevisiae strain SS328-leu, and proven to be functional when oxidative stress is induced by hydrogen peroxide. The TSA1 promoter has a relatively high base level of expression, but expression levels are further driven up when induced.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 290
Illegal SpeI site found at 364 - 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 290
Illegal SpeI site found at 364 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 453
- 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 290
Illegal SpeI site found at 364 - 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 290
Illegal SpeI site found at 364
Illegal NgoMIV site found at 613
Illegal NgoMIV site found at 623 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 158
References
He, X.J. and Fassler, J.S., 2005. Identification of novel Yap1p and Skn7p binding sites involved in the oxidative stress response of Saccharomyces cerevisiae. Molecular microbiology, 58(5), pp.1454-1467.