Difference between revisions of "Part:BBa K3734005"
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<partinfo>BBa_K3734005 short</partinfo> | <partinfo>BBa_K3734005 short</partinfo> | ||
GAL4 is a kind of protein that can find and combined with UAS DNA structure domain. | GAL4 is a kind of protein that can find and combined with UAS DNA structure domain. | ||
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+ | <html> | ||
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+ | <head> | ||
+ | |||
+ | </head> | ||
+ | |||
+ | <body> | ||
+ | <h2 class="pageContent-main__title"> | ||
+ | <!--put tile here, <h2>title</h2>, class="pageContent-main__title" means it is the main title--> | ||
+ | GAL4 | ||
+ | </h2> | ||
+ | <div class="pageContent-main__textBox"> | ||
+ | <!--all the content must included in this div--> | ||
+ | <p>GAL4 is a common part in double yeast hybrid system. It can recognize and combine with UAS. Because GAL4 is originated from yeast cells, the activation domain can not work in mammalian cells. Therefore, we only used its combining domain | ||
+ | and use it together with VP16 which is an activation domain comes from virus to realize the activation of downstream UAS transcription | ||
+ | </p> | ||
+ | </div> | ||
+ | <h2 class="pageContent-main__title pageContent-main__subtitle"> | ||
+ | <!--class="pageContent-main__title" means it is the sub title--> | ||
+ | 1.Pattern diagram | ||
+ | </h2> | ||
+ | <div class="pageContent-main__textBox"> | ||
+ | <!--all the content must included in this div--> | ||
+ | <img class="image" src="https://2021.igem.org/wiki/images/8/87/T--CSU_CHINA--tupian5.png"> | ||
+ | <!--put image's url here--> | ||
+ | <p style="width: 80%;text-align:center;font-size: .9rem; margin: -1rem auto 1rem auto; color: #888;">Fig.1 The model diagram of GIP-miR21T-GI-GAL4-4XmiR21T</p> | ||
+ | </div> | ||
+ | <h2 class="pageContent-main__title pageContent-main__subtitle"> | ||
+ | <!--class="pageContent-main__title" means it is the sub title--> | ||
+ | 2.Caution | ||
+ | </h2> | ||
+ | <div class="pageContent-main__textBox"> | ||
+ | <!--all the content must included in this div--> | ||
+ | <p>GAL4 combining domain is universal among eukaryotic cells, but the activation factor needs to be chosen differently according to the chassis creature. | ||
+ | </p> | ||
+ | </div> | ||
+ | <h2 class="pageContent-main__title pageContent-main__subtitle"> | ||
+ | <!--class="pageContent-main__title" means it is the sub title--> | ||
+ | Reference: | ||
+ | </h2> | ||
+ | <div class="pageContent-main__textBox"> | ||
+ | <!--all the content must included in this div--> | ||
+ | <p>[1]Chun Jeih Ryu , Charles E Whitehurst, Jianzhu Chen.Expression of Gal4-VP16 and Gal4-DNA binding domain under the control of the T lymphocyte-specific lck proximal promoter in transgenic mice[J].BMB Rep. 2008 Aug 31;41(8):575-80. | ||
+ | </p> | ||
+ | </div> | ||
+ | </body> | ||
+ | </html> | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Latest revision as of 08:39, 20 October 2021
GAL4
GAL4 is a kind of protein that can find and combined with UAS DNA structure domain.
GAL4
GAL4 is a common part in double yeast hybrid system. It can recognize and combine with UAS. Because GAL4 is originated from yeast cells, the activation domain can not work in mammalian cells. Therefore, we only used its combining domain and use it together with VP16 which is an activation domain comes from virus to realize the activation of downstream UAS transcription
1.Pattern diagram
Fig.1 The model diagram of GIP-miR21T-GI-GAL4-4XmiR21T
2.Caution
GAL4 combining domain is universal among eukaryotic cells, but the activation factor needs to be chosen differently according to the chassis creature.
Reference:
[1]Chun Jeih Ryu , Charles E Whitehurst, Jianzhu Chen.Expression of Gal4-VP16 and Gal4-DNA binding domain under the control of the T lymphocyte-specific lck proximal promoter in transgenic mice[J].BMB Rep. 2008 Aug 31;41(8):575-80.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 215
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 134