Difference between revisions of "Team:MIT/Experiments/miRNA"
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Revision as of 06:28, 16 October 2016
How can we detect endometriosis using miRNA?
What is miRNA?
For those who are not familiar with miRNA, miRNA are small units of RNA found in all mammalian cells and play a regular role in gene regulation. miRNA is single stranded and only about 20 nucleotides long. With the help of other proteins(which form what is called the 'RISC complex'), miRNA is guided to a complementary part on the mRNA (miRNA target site) where miRNA binds and cleaves messenger RNA. This inhibits gene expression post transcriptionally.
Why is miRNA a good biomarker?
There are hundreds of different miRNAs that can make up a specific cell's miRNA profile. The profile and activity of miRNA varies between different cell types and different cells states.This makes it is possible to tell the difference between cells from the uterus and liver, and the difference between healthy and diseased cells based on miRNA profiles.
Found in all mammalian cells
Unique to cell type
Unique to cell states
What is the miRNA profile of Endometriosis?
Cells from the uterus (referred to as 'eutopic endometiotic cells') of women with endometriosis have been found to have dysregulated miRNA in comparison to cells from the uterus of women who do not have endometriosis (referred to as 'eutopic endometrial cells')[]. In order to study the uses of these miRNAs in our circuit, eight candidates were chosen based on fold difference in miRNA level between the the endometrial biopsy from women with and without endometriosis. The eight candidates are shown in the table below:
Our circuit utilizes the natural function of miRNA to regulate gene expression. Depending on the miRNA activity in a cell, different levels of our desired gene will be expressed. This allows our circuit to produce a differential output depending on whether the cell has dysregulated miRNA. This is achieved by attaching 4 tandem sites complementary to the affected miRNA following a gene of interest. This is called the miRNA target site (miRNA-ts).
These 4 tandem sites for miRNA binding were tested by coding for them distal to the gene for red fluorescent protein. We were able to see a ten fold repression upon increasing the concentration of siRNA from 0 to 1 nM. Saturation appeared at about 10 nM.
How can our circuit sense miRNA activity?
Read more about our decision to use miRNA sensors
Are the target sites sensitive to miRNA levels?
Read more about our experiment testing miRNA target site sensitivity
Probing tHESC for miRNA Levels
Unlike more common cell lines like MCF7 and HEK293, tHESC is not a highly characterized cell line. This meant that the levels of our eight miRNA candidates were completely unknown in tHESC. We set out to characterize our miRNA target sites (miRNA-ts) in tHESC using a miRNA sensor.
What is tHESC?
Read more about our experiment to characterize miRNA targets sites in tHESC
