Difference between revisions of "Team:TokyoTech/Experiment/Chimeric Transcription Factor"

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     <p style="font-family: Poppins;font-size: 16px">In this assay, we checked whether human cells (<span style="font-style: italic">EA.hy926</span> cell) receive AHL, a signaling molecule derived from <i>E. coli</i> and induce the transcription of <i>atlPT4</i> gene and <i>log1</i> gene which synthesize iP. Also, we checked whether IP (Isopentenyl adenine) molecules are synthesized in <span style="font-style: italic">EA.hy926</span> cells by TLC.
+
     <p style="font-family: Poppins;font-size: 16px">In this assay, we investigated whether human cells (<span style="font-style: italic">EA.hy926</span> cell) receive AHL, a signaling molecule that is synthesized in and exported from <span style="font-style: italic">E. coli</span> and induce the transcription of <span style="font-style: italic">atIPT4</span> and <span style="font-style: italic">log1</span> genes to synthesize iP.
 
     </p>
 
     </p>
 
     <br>
 
     <br>
 
     <p style="font-family: Poppins;font-size: 16px"><u>Note</u></p>
 
     <p style="font-family: Poppins;font-size: 16px"><u>Note</u></p>
     <p style="font-family: Poppins;font-size: 16px">AHLs, which stand for [N-]acyl-homoserine lactones, are small signaling molecules and are employed in the bacterial “Quorum Sensing”. Among several kinds of the signaling molecules, we used 3OC8AHL(C8) in the assay.</p>
+
     <p style="font-family: Poppins;font-size: 16px">AHLs, which stand for [N-]acyl-homoserine lactones, are small signaling molecules and are employed in the bacterial “Quorum Sensing”. Among several kinds of AHLs, 3OC8HSL(C8) was employed in the assay.
 +
 
 +
Isopentenyl adenine (iP) is a kind of cytokinin and we use it as a signal molecule from human cells to <span style="font-style: italic">E. coli</span> in the inter-kingdom communication. Cytokinins are the signaling molecules (or Phytohormones) that plants produce and play important roles in cell growth and differentiation. In the case of Arabidopsis thaliana, extracellular iP is received by a transmembrane receptor, AHK4. AHK4 has a histidine kinase activity, and binding of iP to AHK4 triggers auto-phosphorylation of AHK4 and the following histidine-to-aspartate phosphorelay. As a consequence, transcription from target genes is induced and/or repressed so that physiological states of plants are changed. The histidine kinase activity of AHK4 has shown to be activated depending on iP even in <span style="font-style: italic">E. coli</span> cells (Suzuki et al. 2001, Lukáš Spíchal et al. 2004). This fact encouraged us to use iP as a signaling molecule in our project (See AHK4 Assay page).</p>
  
 
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     <p style="font-family: Poppins;font-size: 16px">As shown in Fig. , we introduced two kinds of constructs into <span style="font-style: italic">EA.hy926</span> cells by electroporation. CAG promoter constantly expresses relA/NLS/traR. After the protein binds with 3OC8AHL(C8), the complex exposes nuclear localization signal and activates CMVmin promoter in CMVmin_atIPT4_IVS_IRES_LOG1_polyA. As a result of pCMVmin's activation, downstream <i>atlPT4</i> gene and <i>log1</i> gene are transcripted. <i>atlPT4</i> gene and <i>log1</i> gene jointly work as IP synthetase.
+
     <p style="font-family: Poppins;font-size: 16px">As shown in Fig.1, two kinds of constructs were introduced into <span style="font-style: italic">EA.hy926</span> cells by electroporation. The CAG promoter (pCAG) constantly expresses the chimeric protein, <span style="font-style: italic"> relA/NLS/traR</span>. When <span style="font-style: italic"> relA/NLS/traR</span> binds with C8, this complex binds to (tra box)7 sequence (the enhancer sequence; see below) and activates transcription from the CMV minimal promoter (CMV min). As a result, at the <span style="font-style: italic">atIPT4</span> and <span style="font-style: italic">log1</span> genes are transcribed depending on C8. The <span style="font-style: italic">atIPT4</span> and <span style="font-style: italic">log1</span> gene products jointly work as IP synthetase.
 +
 
 
     </p>
 
     </p>
  
 
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       <figure>
 
       <figure>
       <img src="https://static.igem.org/mediawiki/2017/1/15/T--TokyoTech--human_cell_circuit.png" style="max-width:50%">
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       <img src="https://static.igem.org/mediawiki/2017/1/15/T--TokyoTech--human_cell_circuit.png" style="max-width:75%">
       <figcaption style="font-family: Poppins;font-size: 16px">Fig. 画像タイトル</figcaption>
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       <figcaption style="font-family: Poppins;font-size: 16px">Fig1. Construction of iP synthetase genes</figcaption>
 
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     <figure>
 
     <figure>
     <img src="https://static.igem.org/mediawiki/2017/f/f9/T--TokyoTech--human_cell_results_1022.png" style="max-width:50%">
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     <img src="https://static.igem.org/mediawiki/2017/e/e1/Human_cell_assay_result_tokyotech.png" style="max-width:100%">
     <figcaption style="font-family: Poppins;font-size: 16px">Fig. 画像タイトル</figcaption>
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     <figcaption style="font-family: Poppins;font-size: 16px">Fig2. Result of the qualitative experiment</figcaption>
 
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     <h1 class="w3-xxxlarge w3-text-red" style="padding-bottom: 10px;padding-top: 10px"><b>Discussion</b></h1>
 
     <h1 class="w3-xxxlarge w3-text-red" style="padding-bottom: 10px;padding-top: 10px"><b>Discussion</b></h1>
 
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     <p style="font-family: Poppins;font-size: 16px">We checked the transcription of <i>atlPT4</i> gene and <i>log1</i> gene are induced by C8 addition and the induction depends on C8 concentration.
+
     <p style="font-family: Poppins;font-size: 16px">We confirmed that the transcription of <span style="font-style: italic">atIPT4</span> and <span style="font-style: italic">log1</span> genes are induced by C8 addition and the degree of induction depends on C8 concentration.
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     </p>
 
     </p>
  

Revision as of 12:22, 30 October 2017

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iGEM Tokyo Tech

Chimeric Transcription Factor Assay


Introduction


In this assay, we investigated whether human cells (EA.hy926 cell) receive AHL, a signaling molecule that is synthesized in and exported from E. coli and induce the transcription of atIPT4 and log1 genes to synthesize iP.


Note

AHLs, which stand for [N-]acyl-homoserine lactones, are small signaling molecules and are employed in the bacterial “Quorum Sensing”. Among several kinds of AHLs, 3OC8HSL(C8) was employed in the assay. Isopentenyl adenine (iP) is a kind of cytokinin and we use it as a signal molecule from human cells to E. coli in the inter-kingdom communication. Cytokinins are the signaling molecules (or Phytohormones) that plants produce and play important roles in cell growth and differentiation. In the case of Arabidopsis thaliana, extracellular iP is received by a transmembrane receptor, AHK4. AHK4 has a histidine kinase activity, and binding of iP to AHK4 triggers auto-phosphorylation of AHK4 and the following histidine-to-aspartate phosphorelay. As a consequence, transcription from target genes is induced and/or repressed so that physiological states of plants are changed. The histidine kinase activity of AHK4 has shown to be activated depending on iP even in E. coli cells (Suzuki et al. 2001, Lukáš Spíchal et al. 2004). This fact encouraged us to use iP as a signaling molecule in our project (See AHK4 Assay page).


Summary


As shown in Fig.1, two kinds of constructs were introduced into EA.hy926 cells by electroporation. The CAG promoter (pCAG) constantly expresses the chimeric protein, relA/NLS/traR. When relA/NLS/traR binds with C8, this complex binds to (tra box)7 sequence (the enhancer sequence; see below) and activates transcription from the CMV minimal promoter (CMV min). As a result, at the atIPT4 and log1 genes are transcribed depending on C8. The atIPT4 and log1 gene products jointly work as IP synthetase.

Fig1. Construction of iP synthetase genes

Results


文章

Fig2. Result of the qualitative experiment

Discussion


We confirmed that the transcription of atIPT4 and log1 genes are induced by C8 addition and the degree of induction depends on C8 concentration.


Reference


Petra Neddermann, Cesare Gargioli, Ester Muraglia, Sania Sambuncini, Fabio Bonelli, Raffaele De Francesco, Riccardo cortese (2003) A novel, inducible, eukaryotic gene expression system based on the quorum-sensing transcription facter TraR. EMBO reports VOL 4: 159-165.

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