Team:DTU-Denmark-2/results/Proofofconcept/fungi

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<b>Proof of concept in fungi</b><br> <br>  
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<b>Proof of concept - Fungi</b><br> <br>  
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Several separate devices were conducted with Plug ‘n’ Play assembly to verify if the system will work in fungi as well as in mammalian cells. The idea was to target the fungi with a fluorescence protein to specific compartments and in general to express the fluorescence proteins. All the devices have the same promoter, terminator and marker cassette, though with different gene of interest and were all transformed in laboratory <i> Aspergillus nidulans</i> stain:<i> argB2, pyrG89, veA1</i> by random non-homologues-end-joining integration. 
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<a href="https://2011.igem.org/Team:DTU-Denmark-2/results/Proofofconcept/fungi#Proof of concept" class="h1">Proof of concept</a><br><br>
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<a href="https://2011.igem.org/Team:DTU-Denmark-2/results/Proofofconcept/fungi#pJEJAM12 BBa_K678060" class="h2"> pJEJAM12<br>
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BBa_K678060</a><br><br>
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<a href="https://2011.igem.org/Team:DTU-Denmark-2/results/Proofofconcept/fungi#pJEJAM13 BBa_K678061" class="h2"> pJEJAM13 <br>
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BBa_K678061</a><br><br>
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<a href="https://2011.igem.org/Team:DTU-Denmark-2/results/Proofofconcept/fungi#pJEJAM14 BBa_K678062" class="h2"> pJEJAM14 <br>
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BBa_K678062</a><br><br>
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<a href="https://2011.igem.org/Team:DTU-Denmark-2/results/Proofofconcept/fungi#pJEJAM15 BBa_K678063" class="h2"> pJEJAM15 <br>
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BBa_K678063</a><br><br>
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<a href="https://2011.igem.org/Team:DTU-Denmark-2/results/Proofofconcept/fungi#Wild type" class="h2"> Wild type</a><br><br>
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<a name="Proof of concept"></a><h1><b>Proof of concept</b></h1>
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Five different plasmids were constructed with the Plug 'n' Play assembly standard in order to verify the systems function in filamentous fungi. To ensure a successful transformation the backbone plasmid <a href="http://partsregistry.org/Part:BBa_K678046">pFun</a> has two NotI restriction sites flanking the device to be inserted. Hereby, the device can be cut out of the plasmid and the linearized DNA fragments can be transformed into the fungus. The devices for proof of concept are not designed to be inserted at a specific site in the fungal genome. Therefore, the device can be integrated at any site and with a random number of copies by non-homologous end joining (NHEJ). This means that the possibility of the disruption of essential genes exists.<br><br>
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The fungal proof of concept plasmids, were constructed with the strong constitutive promoter <a href="http://partsregistry.org/Part:BBa_K678024">P<i>gpdA</i></a>, the <a href="http://partsregistry.org/Part:BBa_K678036">T<i>trpC</i></a> terminator, and the <a href="http://partsregistry.org/Part:BBa_K678040"><i>pyrG marker cassette</i></a>. Different genes encoding fluorescent proteins were included in the reporter system, where different compartments of fungi could be targeted. The reporter system was designed to target the nucleus, peroxisomes, and the mitochondria. All transformations were performed in the <i> Aspergillus nidulans</i> laboratory strain:<i> argB2, pyrG89, veA1</i>. </p>
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We succeed in proving that Plug ‘n’ Play assembly easily transformed and expressed in fungi as we succeed in tagging A. nidulans with two fluorescence proteins. The transformants with integration of our 4 devices change morphology compared with the wild type control strain since the DNA were randomly intergraded and have inflicted some pathways in the fungi.
 
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The results are displayed in the following section.
 
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We here prove that the Plug 'n' Play assembly standard can easily be applied for the construction fungal plasmids. The constructed plasmids were transformed into <i>A. nidulans</i> and in each case the fluorescent protein was expressed. Only the strain transformed with <a href="http://partsregistry.org/Part:BBa_K678064">pJEJAM16</a> targeting GFP to the mitochondria did not result in any transformants and due to time limitation the experiment was not repeated.<br><br>
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The obtained transformants with the different constructed devices integrated into the genome all had a different morphology and were growing slower than the wild type strain. Especially the strain transformed with pJEJAM14 looked sick. The fungi also had a pronounced number of undefined vacuoles that can be seen on the images obtained from differential interference contrast (DIC) microscopy. Such 'symptoms' are not uncommon when DNA is introduced into the genome by NHEJ. Below the images of the microscopy are presented.
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<a name="pJEJAM12 BBa_K678060"></a><h2>pJEJAM12 BBa_K678060</h2>
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<a href="http://partsregistry.org/Part:BBa_K678060">pJEJAM12</a> is a plasmid intended for linearization and transformation into <i>A. nidulans</i>. The plasmid contains the gene encoding green fluorescent protein (GFP) under the control of the strong constitutive P<i>gpdA</i> promoter. The expressed GFP was evenly spread in the hyphae.
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<b>Device 22</b><br>
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The results shows fluorescence spread evenly in the hyphae which correlate with that in device 22, the gene of interest, only consists of a green fluorescence protein GFP with no specific target.
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<img src="https://static.igem.org/mediawiki/2011/2/20/Device_22.png" height="110px" align="center"> </img>
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<td><img src="https://static.igem.org/mediawiki/2011/4/45/22_dic_3_png.png" height="200px"> </img></td>
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<img src="https://static.igem.org/mediawiki/2011/4/45/22_dic_3_png.png" height="250px" align="center"> </img>
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<td><img src="https://static.igem.org/mediawiki/2011/7/72/22_GFP_colour_best_fit_3.jpg" height="200px"> </img></td>
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<img src="https://static.igem.org/mediawiki/2011/e/eb/22_YFP3_colour_best_fit.jpg" height="250px" align="center"> </img>
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<td>DIC image of<i> Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678060">pJEJAM12</a>.</td>
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<td><i>Aspergillus nidulans </i> with device 22 - DIC light.</td>
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<td>Fluorescence image of <i>Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678060">pJEJAM12</a>.</td>
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<td><i>Aspergillus nidulans </i> with device 22 - YFP light.</td>
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<td><img src="https://static.igem.org/mediawiki/2011/1/12/22-7_back.jpeg" height="200px" align="center"> </img></td>
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<img src="https://static.igem.org/mediawiki/2011/8/8e/22-7_back_rettet.jpg" height="250px" align="center"> </img>
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<td><i>Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678060">pJEJAM12</a> - Shown from front</td>
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<td><i>Aspergillus nidulans </i> with device 22 - Front</td>
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<td><i>Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678060">pJEJAM12</a> - Shown from Back </td>
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<td><i>Aspergillus nidulans </i> with device 22 - Back </td>
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<a name="pJEJAM13 BBa_K678061"></a><h2>pJEJAM13 BBa_K678061</h2>
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<a href="http://partsregistry.org/Part:BBa_K678061">pJEJAM13</a> is a plasmid intended for linearization and transformation into <i>A. nidulans</i>. The plasmid contains the gene encoding green fluorescent protein (GFP) with the peroxisomal targeting sequence 1 (PTS1) fused to the C-terminus, under the control of the strong constitutive P<i>gpdA</i> promoter.</p>
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<b>Device 23</b><br>
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The results shows fluorescence spread evenly in the hyphae and with spots of fluorescence. Device 23 consists of GFP with a target signal to the peroxisomes which can explain the spots compared to the results from device 22. We cannot conclude that the signal is accumulated in the peroxisomes since they are not dyed, though can it be concluded that the GFP signal is target a specific place and accumulated somewhere in the fungi compared to the results from device 22.
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<img src="https://static.igem.org/mediawiki/2011/9/99/Device_23.png" height="110px" align="center"> </img>
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Green fluorescence can be observed in the hyphae and in clear spots. This indicates that GFP is targeted to the peroxisomes, but further investigations are required to confirm this. The 'background' fluorescence was however not expected and a replication of the experiment should be conducted in order to be able to draw any conclusions upon this. </p>
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<td><img src="https://static.igem.org/mediawiki/2011/8/88/23_dic4_png.png" height="200px" align="center"> </img></td>
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<img src="https://static.igem.org/mediawiki/2011/f/fb/23_YFP_colour_dots-2.jpg" height="250px" align="center"> </img>
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<td>DIC image of <i>Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678061">pJEJAM13</a>.</td>
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<td><i>Aspergillus nidulans </i> with device 23 - DIC light.</td>
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<td>Fluorescence image of <i>Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678061">pJEJAM13</a>. Green fluorescence can be observed in the hyphae and in clear spots.</td>
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<td><i>Aspergillus nidulans </i> with device 23 - YFP light.</td>
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<td><img src="https://static.igem.org/mediawiki/2011/e/eb/23-11_front_rettet.jpg" height="200px" align="center"> </img></td>
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<td><i>Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678061">pJEJAM13</a> - Shown from front</td>
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<td><i>Aspergillus nidulans </i> with device 23 - Front</td>
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<td><i>Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678061">pJEJAM13</a> - Shown from back </td>
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<td><i>Aspergillus nidulans </i> with device 23 - Back </td>
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<b>Device 24</b><br>
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<a name="pJEJAM14 BBa_K678062"></a><h2>pJEJAM14 BBa_K678062</h2>
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<a href="http://partsregistry.org/Part:BBa_K678062">pJEJAM14</a> is a plasmid intended for linearization and transformation into <i>A. nidulans</i>. The plasmid contains the gene encoding monomeric red fluorescent protein (mRFP1) under the control of the strong constitutive P<i>gpdA</i> promoter. The expressed mRFP1 was evenly spread in the hyphae.
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The results shows fluorescence spread evenly in the hyphae which correlate with that in device 23, the gene of interest, only consists of a green fluorescence protein RFP with no specific target.
 
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<img src="https://static.igem.org/mediawiki/2011/8/8b/Device_24.png" height="125px" align="center"> </img>
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<img src="https://static.igem.org/mediawiki/2011/a/aa/Device_24_ny.png" height="100px" align="center"> </img>
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<td><img src="https://static.igem.org/mediawiki/2011/b/b9/24_dic_t_1_png.png" height="200px" align="center"> </img></td>
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<img src="https://static.igem.org/mediawiki/2011/b/b9/24_dic_t_1_png.png" height="250px" align="center"> </img>
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<td><img src="https://static.igem.org/mediawiki/2011/5/52/24_RFP_1_colour.jpg" height="200px" align="center"> </img></td>
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<td>DIC image of <i>Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678062">pJEJAM14</a>.</td>
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<td><i>Aspergillus nidulans </i> with device 24 - DIC light.</td>
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<td>Fluorescence image of <i>Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678062">pJEJAM14</a>.</td>
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<td><i>Aspergillus nidulans </i> with device 24 - RFP light.</td>
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<td><i>Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678062">pJEJAM14</a> - shown from front</td>
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<td><i>Aspergillus nidulans </i> with device 24 - Front</td>
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<td><i>Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678062">pJEJAM14</a> - shown from back </td>
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<td><i>Aspergillus nidulans </i> with device 24 - Back </td>
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<b>Device 25</b><br>
 
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The results show spots of fluorescence as in Device 23. Device 25 consists of RFP with a target signal to the nucleus which can explain the spots compared to the results from device 22 and the spores with a single nuclei contains a lot of RFP signal. We cannot conclude that the signal is accumulated in the nucleus since they are not dyed, though can it be concluded that the RFP signal is target a specific place and accumulated somewhere.
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<a name="pJEJAM15 BBa_K678063"></a><h2>pJEJAM15 BBa_K678063</h2>
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<a href="http://partsregistry.org/Part:BBa_K678063">pJEJAM15</a> is a plasmid intended for linearization and transformation into <i>A. nidulans</i>. The plasmid contains the gene encoding monomeric red fluorescent protein (mRFP1) with a nucleosomal targeting sequence (NLS) fused to the C-terminus, under the control of the strong constitutive P<i>gpdA</i> promoter.</p> Red fluorescence can be observed in clear spots. To confirm that the mRFP1 in fact is targeted to the nucleus further experiments have to be conducted. </p>
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<img src="https://static.igem.org/mediawiki/2011/a/ac/Device_25.png" height="125px" align="center"> </img>
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<td><img src="https://static.igem.org/mediawiki/2011/9/91/25_RFP_3-t%C3%B8r_colour_-2.jpg" height="200px" align="center"> </img></td>
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<img src="https://static.igem.org/mediawiki/2011/9/91/25_RFP_3-t%C3%B8r_colour_-2.jpg" height="250px" align="center"> </img>
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<td>DIC image of<i>Aspergillus nidulans </i> with <br><a href="http://partsregistry.org/Part:BBa_K678063">pJEJAM15</a>.</td>
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<td><i>Aspergillus nidulans </i> with device 25 - DIC light.</td>
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<td>Fluorescence image of <i>Aspergillus nidulans </i><br><a href="http://partsregistry.org/Part:BBa_K678063">pJEJAM15</a>.</td>
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<td><i>Aspergillus nidulans </i> with device 25 - RFP light.</td>
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<img src="https://static.igem.org/mediawiki/2011/2/2f/25.14_front_rettet.jpg" height="250px" align="center"> </img>
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<td><img src="https://static.igem.org/mediawiki/2011/c/c8/25.14_back_rettet.jpg" height="200px" align="center"> </img></td>
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</td>
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<td>
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<img src="https://static.igem.org/mediawiki/2011/c/c8/25.14_back_rettet.jpg" height="250px" align="center"> </img>
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-
</td>
+
</tr>
</tr>
<tr>
<tr>
-
 
+
<td><i>Aspergillus nidulans </i> with <br> <a href="http://partsregistry.org/Part:BBa_K678063">pJEJAM15</a> - Shown from front</td>
-
<td><i>Aspergillus nidulans </i> with device 25 - Front</td>
+
<td><i>Aspergillus nidulans </i> with <br> <a href="http://partsregistry.org/Part:BBa_K678063">pJEJAM15</a> - Shown from back </td>
-
 
+
-
<td><i>Aspergillus nidulans </i> with device 25 - Back </td>
+
</tr>
</tr>
</table>
</table>
</p>
</p>
 +
<br>
<br>
<br>
<br>
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<font color="#990000" face="arial" size="6" >
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<a name="Wild type"></a><h2>Wild type</h2>
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<p align="center">
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<b>Control</b><br>
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</p>
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</font>
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The control strain shows no auto-fluorescence.
+
The wild type strain shows no background or auto-fluorescence.
<p align="center">
<p align="center">
<table cellpadding="10px" align="center">
<table cellpadding="10px" align="center">
<tr>
<tr>
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<td>
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<td><img src="https://static.igem.org/mediawiki/2011/b/ba/Kontrol_dic_4.png" height="150px" alt="""/></td>
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<img src="https://static.igem.org/mediawiki/2011/b/ba/Kontrol_dic_4.png" height="200px" alt="""/>
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<td><img src="https://static.igem.org/mediawiki/2011/6/6d/Kontrol_rfp_4_P.png" height="150px" alt="""/></td>
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</td>
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<img src="https://static.igem.org/mediawiki/2011/6/6d/Kontrol_rfp_4_P.png" height="200px" alt="""/>
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<img src="https://static.igem.org/mediawiki/2011/c/cb/Kontrol_yfp_4_pp.png" height="200px" alt="""/>
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</td>
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<tr>
<tr>
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<td> DIC image of wild type <i>Aspergillus nidulans </i>. <br></td>
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<td> Wild type <i>Aspergillus nidulans </i> - DIC light. </td>
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<td>RFP fluorescence image of wild type <i>Aspergillus nidulans </i>. <br> </td>
-
 
+
<td>GFP fluorescence image of wild type <i>Aspergillus nidulans </i>.<br></td>
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<td>Wild type <i>Aspergillus nidulans </i> - RFP light. </td>
+
-
 
+
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<td>Wild type <i>Aspergillus nidulans </i> - YFP light.</td>
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<table cellpadding="10px" align="center">
<table cellpadding="10px" align="center">
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<img src="https://static.igem.org/mediawiki/2011/b/bf/Nid_5.jpg" height="250px" align="center"> </img>
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<td><img src="https://static.igem.org/mediawiki/2011/6/67/Nid_5_back.jpg" height="200px" align="center"> </img></td>
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<img src="https://static.igem.org/mediawiki/2011/6/67/Nid_5_back.jpg" height="250px" align="center"> </img>
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</td>
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</tr>
</tr>
<tr>
<tr>
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<td>Wild type <i>Aspergillus nidulans </i> <br>- Shown from front</td>
 +
<td>Wild type <i>Aspergillus nidulans </i> <br>- Shown from back </td>
 +
</tr>
 +
</table>
-
<td>Wild type <i>Aspergillus nidulans </i> - Front</td>
 
-
<td>Wild type <i>Aspergillus nidulans </i> - Back </td>
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</td>
</tr>
</tr>
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Latest revision as of 20:04, 21 September 2011




Proof of concept - Fungi


Proof of concept

Five different plasmids were constructed with the Plug 'n' Play assembly standard in order to verify the systems function in filamentous fungi. To ensure a successful transformation the backbone plasmid pFun has two NotI restriction sites flanking the device to be inserted. Hereby, the device can be cut out of the plasmid and the linearized DNA fragments can be transformed into the fungus. The devices for proof of concept are not designed to be inserted at a specific site in the fungal genome. Therefore, the device can be integrated at any site and with a random number of copies by non-homologous end joining (NHEJ). This means that the possibility of the disruption of essential genes exists.

The fungal proof of concept plasmids, were constructed with the strong constitutive promoter PgpdA, the TtrpC terminator, and the pyrG marker cassette. Different genes encoding fluorescent proteins were included in the reporter system, where different compartments of fungi could be targeted. The reporter system was designed to target the nucleus, peroxisomes, and the mitochondria. All transformations were performed in the Aspergillus nidulans laboratory strain: argB2, pyrG89, veA1.


We here prove that the Plug 'n' Play assembly standard can easily be applied for the construction fungal plasmids. The constructed plasmids were transformed into A. nidulans and in each case the fluorescent protein was expressed. Only the strain transformed with pJEJAM16 targeting GFP to the mitochondria did not result in any transformants and due to time limitation the experiment was not repeated.

The obtained transformants with the different constructed devices integrated into the genome all had a different morphology and were growing slower than the wild type strain. Especially the strain transformed with pJEJAM14 looked sick. The fungi also had a pronounced number of undefined vacuoles that can be seen on the images obtained from differential interference contrast (DIC) microscopy. Such 'symptoms' are not uncommon when DNA is introduced into the genome by NHEJ. Below the images of the microscopy are presented.




pJEJAM12 BBa_K678060

pJEJAM12 is a plasmid intended for linearization and transformation into A. nidulans. The plasmid contains the gene encoding green fluorescent protein (GFP) under the control of the strong constitutive PgpdA promoter. The expressed GFP was evenly spread in the hyphae.




DIC image of Aspergillus nidulans with
pJEJAM12.
Fluorescence image of Aspergillus nidulans with
pJEJAM12.

Aspergillus nidulans with
pJEJAM12 - Shown from front
Aspergillus nidulans with
pJEJAM12 - Shown from Back



pJEJAM13 BBa_K678061

pJEJAM13 is a plasmid intended for linearization and transformation into A. nidulans. The plasmid contains the gene encoding green fluorescent protein (GFP) with the peroxisomal targeting sequence 1 (PTS1) fused to the C-terminus, under the control of the strong constitutive PgpdA promoter.




Green fluorescence can be observed in the hyphae and in clear spots. This indicates that GFP is targeted to the peroxisomes, but further investigations are required to confirm this. The 'background' fluorescence was however not expected and a replication of the experiment should be conducted in order to be able to draw any conclusions upon this.



DIC image of Aspergillus nidulans with
pJEJAM13.
Fluorescence image of Aspergillus nidulans with
pJEJAM13. Green fluorescence can be observed in the hyphae and in clear spots.
Aspergillus nidulans with
pJEJAM13 - Shown from front
Aspergillus nidulans with
pJEJAM13 - Shown from back



pJEJAM14 BBa_K678062

pJEJAM14 is a plasmid intended for linearization and transformation into A. nidulans. The plasmid contains the gene encoding monomeric red fluorescent protein (mRFP1) under the control of the strong constitutive PgpdA promoter. The expressed mRFP1 was evenly spread in the hyphae.




DIC image of Aspergillus nidulans with
pJEJAM14.
Fluorescence image of Aspergillus nidulans with
pJEJAM14.
Aspergillus nidulans with
pJEJAM14 - shown from front
Aspergillus nidulans with
pJEJAM14 - shown from back



pJEJAM15 BBa_K678063

pJEJAM15 is a plasmid intended for linearization and transformation into A. nidulans. The plasmid contains the gene encoding monomeric red fluorescent protein (mRFP1) with a nucleosomal targeting sequence (NLS) fused to the C-terminus, under the control of the strong constitutive PgpdA promoter.

Red fluorescence can be observed in clear spots. To confirm that the mRFP1 in fact is targeted to the nucleus further experiments have to be conducted.




DIC image ofAspergillus nidulans with
pJEJAM15.
Fluorescence image of Aspergillus nidulans
pJEJAM15.
Aspergillus nidulans with
pJEJAM15 - Shown from front
Aspergillus nidulans with
pJEJAM15 - Shown from back



Wild type

The wild type strain shows no background or auto-fluorescence.

DIC image of wild type Aspergillus nidulans .
RFP fluorescence image of wild type Aspergillus nidulans .
GFP fluorescence image of wild type Aspergillus nidulans .
Wild type Aspergillus nidulans
- Shown from front
Wild type Aspergillus nidulans
- Shown from back