Team:Shenzhen BGIC ATCG/modeling

From 2013.igem.org

(Difference between revisions)
Line 149: Line 149:
<h4>SIC1_Art on G1 stage</h4>
<h4>SIC1_Art on G1 stage</h4>
<h5>G1 length:</h5>
<h5>G1 length:</h5>
 +
<p>To understand the temporal effect of SIC1_Art on the length G1 phase, we performed parameter scan on the amount of time of adding SIC1_Art (DeltaT). By setting Ka=0.12 and Kd=0.016, we estimated the relationship between DeltaT and the length of G1 phase. Our computation simulation showed that, as we added SIC1_Art into the yeast, the amount of SIC1_Art will increase at first, and then it will enter a plateau stage. After the plateau stage, SIC1_Art will decrease gradually, which subsequently followed by the leaving of G1 stage (900 min). Our result suggests a positive correlation between DeltaT and the length of G1 phase in the first 900 min, and we discovered an upper bound at the length of G1 phase.
 +
</p>
     </div>
     </div>

Revision as of 18:27, 26 September 2013


Ball Ball

Playing with my eyes
aren't you?

Hi I am Dr. Mage!
A "budding" yeast cell!

Blueprint

Our project based a lot on cell cycle, especially the cyclin-promoters and cyclin-degradation tags. Through modelling Cell cycle is one of the most complex network in biology world. Better understanding of cell cycle and it’s regulation, to some extent, faciliate the fermentation industry because we can easily accelarate or decelarate a cell cycle or even one phase in the cycle which are important for metabolism product synthesis. In order to simulation and predict the experimets of the effeciency of Sic1, alternative splicing and degradation tags in the whole cell cycle, we build tree ordinary differential equation system models.

Cell Cycle

Cell Synchronization

Previously study reported the introduction of sic1p could prevent the cell to enter S phase. Based on the sic1 system in yeast, we developed an artificial sic1 system (SIC1_Art). By adding galactose or modifying the phosphorylated sites, we can regulate the synthesis (Ka) and degradation (Kd) rates of the sic1_Art. We are trying to utilize this artificial system to precisely regulate the phase in yeast cell cycle, and our goal is to understand the synchronization behavior in yeast.

SIC1_Art on G1 stage

G1 length:

To understand the temporal effect of SIC1_Art on the length G1 phase, we performed parameter scan on the amount of time of adding SIC1_Art (DeltaT). By setting Ka=0.12 and Kd=0.016, we estimated the relationship between DeltaT and the length of G1 phase. Our computation simulation showed that, as we added SIC1_Art into the yeast, the amount of SIC1_Art will increase at first, and then it will enter a plateau stage. After the plateau stage, SIC1_Art will decrease gradually, which subsequently followed by the leaving of G1 stage (900 min). Our result suggests a positive correlation between DeltaT and the length of G1 phase in the first 900 min, and we discovered an upper bound at the length of G1 phase.

Alternative Splicing by CRISPRi


Degradation Rate

Degradation tags were also obtained from cyclins because cyclins should degrade fast enough to avoid binding to cdc28 and delaying its own phase. From our simulation we can find out that transformed proteins can also be degraded at a convenient speed.

Parameter Table

Parameter

Rate(min-1)

Citation

D(PEST1)

0.12

Chen et al. (2004)

D(PEST2)

0.12

Chen et al. (2004)

D(PEST3)

0.14

Belli, Gari, Aldea, & Herrero (2001)

D(D-box)

Vdb5

Chen et al. (2004)

As Degradation tags could not fully help tell apart each phase by the light of XFP, we built targeting peptide into model to make a more distinguishable visual result. As shown here, we present a 3D simulation result by adding another axis to specify different organelles.