Difference between revisions of "Team:FAU Erlangen/Tour50"

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Our project is only at the beginning so we need more research and further experiments to validate our results.
 
Our project is only at the beginning so we need more research and further experiments to validate our results.
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Where do we see our project in the brightest future?  
 
Where do we see our project in the brightest future?  
 
One new aspect of our project could be the use of not only deacetylases as histone modifying enzymes, but also methylases, acetylases and methyltransferases to alter the chromatin structure. In eukaryotes gene expression is controlled through conserved mechanisms.
 
One new aspect of our project could be the use of not only deacetylases as histone modifying enzymes, but also methylases, acetylases and methyltransferases to alter the chromatin structure. In eukaryotes gene expression is controlled through conserved mechanisms.
Following this, our construct could be tested in plants, cells, mice, etc. to either knockdown or up-regulate.
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Following this, our construct could be used in cell culture or other organisms such as plants, mice, etc. to either knockdown or up-regulate.
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The next step will be to apply the same concept in other living substances like plants, animals or other cell cultures.
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Revision as of 19:10, 18 September 2015

What will the future bring?

“We do what we must, because we can” - GLaDOS, Aperture Science

Expanding into other organisms

Our project is only at the beginning so we need more research and further experiments to validate our results.
Where do we see our project in the brightest future? One new aspect of our project could be the use of not only deacetylases as histone modifying enzymes, but also methylases, acetylases and methyltransferases to alter the chromatin structure. In eukaryotes gene expression is controlled through conserved mechanisms. Following this, our construct could be used in cell culture or other organisms such as plants, mice, etc. to either knockdown or up-regulate.

Helping humans

The main goal, rescuing people from the edge of death. Although it is probably still decades away, using this system might be a key in the war against cancer.
The greatest use could be in the field of oncology, since there might be a chance to down-regulate the oncogenes and up-regulate tumorsuppressor genes. For example one specific use could be for colon cancer, where APC (a tumorsuppressorgene) is mutated. APC is normally used for degradation of beta-Catenin, but in colon cancer APC is no longer functional which leads to a high amount of beta-Catenin in the tumor cells. Beta-Catenin finds its way into the nucleus where it acts as part of a transcription complex which leads to a higher gene expression. Usually this happens in most of the cancer cases, meaning that down-regulation of these mutated genes might help fight cancer.

Continuing on being creative

There are always ways of using anything for completely different ideas than previously intended. We are eager to find out, what other ways people might think of to use this system.

References:

  • http://www.european-biotechnology-news.com/fileadmin/dateien_ebsin/Pictures_News_2013/2014_01_07_Fotolia_7889092_S_Zellkultur.jpg
  • http://www.nationalgeographic.de/thumbnails/lightbox/14/97/00/maus-9714.jpg
  • http://www.invasive.org/images/768x512/1264002.jpg