Team:Johns Hopkins/Research

Yeast Sex Detector

As our inaugural project, we set out to simplify one of the somewhat belaboring tasks in the field of molecular biology: S. cerevisiae mating type elucidation. Baker’s yeast, S. cerevisiae, has become an invaluable eukaryotic model for molecular biology research for many reasons. One, it utilizes many proteins and biological pathways homologous to those in humans. Consequently, investigating these molecules and systems in yeast has provided unparalleled insight into the genetics of humans. Two, because yeast is unicellular and therefore grows fast, it can be studied more readily than many other organisms, especially those of higher eukaryotes. Another useful characteristic of yeast is its ability to exist in populations of different ploidy, either diploid or haploid. The process in which ploidy arises is governed by the yeast mating pathway, which is well studied.

A haploid yeast cell is either mating type ‘a’ (MATa) or mating type ‘α’(MAT α). In the elucidation of biochemical and genetic processes in yeast, many times it is crucial to initiate sporulation of diploid yeast cells. After sporulation occurs, there are four haploid cells; two MATa and two MAT α. To continue analysis, differentiating between the haploid cells is often crucial, and the necessary assay to do this can take 2 to 3 days. We propose to cut this time to a matter of seconds by constructing a plasmid with fluorescent markers that preferentially activate depending on the mating type. If the cell is MATa, one fluorescent protein is produced. If the cell is MATα, another fluorescent protein is produced. Simply shining a UV lamp over the cells will reveal the mating type, allowing for the cells to be easily separated.

Theory

Depending on the specific regulatory factors being produced, a cell will exhibit a given sex, either MATa or MAT α. (Herskowitz 750) The MATa-associated-products are controlled by α1 and α2 transcriptional regulators. The α1 factor promotes the transcription of MATα-associated-proteins and the α2 factor inhibits the production of MATa-associated-proteins.
The MATa cells produce no MATα-associated-proteins due to a lack of α1 to initiate the production of those MATα-associated-proteins. (Sprague 959) It produces only MATa-associated-proteins, partially due to the lack of inhibition by the absense of α2. The a1 factor does not influence the production of MATa-associated-proteins, even though it is present in MATa clls.
The a/α diploid cells have both a1 factor and α2 factor. These two factors work together (physically) to inhibit certain genes, that confers on the diploid cell the ability to only produce diploid-associated-proteins.

The design of the construct would be such that a MATα cell would produce only one fluorescent protein, and in the case of the prototype diagram of our construct, green fluorescent protein (GFP). A MATa cell would produce only RFP. As such we would place a MATα specific promoter in front of the GFP gene, and a MATa specific promoter in front of the RFP gene.
Time permitting we also hope to utilize a third fluorescent protein that activates only in diploids. Furthermore, we hope to add additional control to the system by allowing the genetist the option of completely turning off the fluorescent proteins, so that they do not interfere with his/her own fluorescent experiments.

Another issue associated with this project would be the life span for a fluorescent protein we express. A particular protein, in general, is governed by the N-terminus rule pathway. This pathway involves the amino acid sequence associated with the N-terminus of the selected protein. Depending on the final amino acids of the sequence, the protein will not be labeled for degradation for a given amount of time (Varshavksy 15). This terminal sequence will thus determine the half-life of the protein, or basically the time in which the protein is functionally present in the cell. So by manipulating this sequence we will be able to determine for how long the desired protein will exist. The control of the half-life of the fluorescence proteins used in the sex detector construct is a crucial issue. If the proteins remain functional for too long, it may not be possible to accurately determine if the hploid cells have fused back into diploids. Also, if the proteins lifespan is so short that the signal is very weak, than the detector is less practical. By optimizing this sequence we will be able to engineer the perfect half-life of the fluorescent proteins involved in the detector, and thus increase its efficacy.

Similar to this issue of control is the issue of a control of specific strains of yeast called HO strains. These strains contain an endonuclease that allows them to alter genomic expression of mating regulatory factors after dividing in the haploid state. The problem that exists in this case is that, after changing mating type, the heterogeneous population of a and α cells can now mate, thus reducing haploid numbers. We also propose to manipulate these regulatory factors, mentioned before, to control the mating, and thus the ploidy, of a given population of HO strains. The most efficient way to do this would be to actually prevent the haploid cell from sensing each other, by altering their ability to produce the functional mating pheromones that allow then to sense the reciprocate sex.

The expected outcome of the three sub-projects listed above is a genetic construct that would allow for the efficient sex and ploidy detection of several yeast strains. The outcome of this work, however, would allow the first Johns Hopkins University iGEM team to compete in the 2008 iGEM competition. This would not only be beneficial to the JHU iGEM team, but also be beneficial to the JHU community as a whole by securing a place in the groundbreaking field of synthetic biology, on an international scale.

Experimentation

Coming soon!