Team:Shenzhen BGIC ATCG/modeling

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.

With the use of cyclins' promoters, we got the simulation of period XFP.

Each XFP will finally merge together so it's hard to tell part. So degradation tags were introduced. 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.

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.

Cell Cycle

To make a precise prediction of our project and analyze its feasibility, we build a cell cycle model based on Chen's work Chen et al. (2004). By simulating the periodic cycle, we obtained the promoters we could make use of.

Promoters are selected by observing the appearance and disappearance of proteins shown in cell cycle model.

Both the model and related papers show that cln1, 2 and clb1, 2, 5, 6 appear at a periodic rhythm because of the appearance of their transcription factors. There are some other proteins (such as NET1) shown this features, but their mechanisms are also related to some protein-protein interactions.

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.

Plateau, the definition:

Based on the relation between DeltaT and the cellular level of SIC1_Art, we defined plateau stage as the time space within which the amount of SIC1_Art is less than the maximum SIC_Art amount during the G1 phase (SIC1_Amax) and greater than (SIC1_Amax - Kd*5min). During this time space, the temporal difference of SIC1_Art degradation is less than 5 min, which we considered the minimum requirement of synchronization.

Ka/Kd, Entering Plateau:

To examine the relation between the synthesis and degradation rate and the timing of entering plateau stage (Tp), we performed parameter scan on Ka and Kd. We found that the Tp is negatively correlated with Ka and positively correlated with Kd.

Ka/kd, Length of Plateau:

To further explore the optimal Ka/Kd in SIC1_Art system, we investigated the influence of Ka/Kd on the length of plateau domain (Lp).

Synchronization in yeast cell cycle

Using the result of above analysis, we chose Ka=0.219, Kd=0.048 as the optimal parameters, which give rise to short entering plateau time and long enough plateau stage (Tp = 61 min, Lp=355 min ).

We simulated the multi-cell behavior in yeast cell cycle: we started with cells in different phases, Art_time = 990 min, we added galactose into the systems, which initiated the synthesis of SIC1_Art and subsequently stopped all the cells at G1 phase. At time=1030 min, we stopped adding galactose and subsequently caused fast degradation of SIC1_Art. This process made all the yeasts into the phase and consequently achieved synchronization.

Alternative Splicing by CRISPRi

To predict the alternative outcome, we also made an intron model to show different results due to incubating in different media. In our project, intron can be spliced in two different ways, providing a completely different outcome because of frame-shift, and this result is not a change like 1-0 to 0-1, but somehow more like a change between 0.4-0.6 and 0.8-0.2.

Reactions:

Parameter Table:

There are 4 parameters that we cannot find during our research, including kass, kdis representing the association and dissociation rate of CRISPRi system, and kass1 and kdis1 representing the association and dissociation rate of Hub1p and spliceosome.

We run parameter scan for each system individually, and found out that with CRISPRi system is more efficient with higher kass and lower kdis, as expected.

And about the alternative splicing model, we attempted to fit simulation result to experimental one. In Hub1 expressed system, L-mRNA will rise at first but descend to an equilibrium stage while S-mRNA will directly rise to its own equilibrium stage.

kass1 should be larger than kdis1, or L-mRNA will be produced more than S-mRNA instead of a ratio of 40-60.

Also, kass1 should not be too smaller than kdis1, or their ratio will be much larger than 40-60.

Finally we set down that kass1 = kdis1.

When inhibiting the expression of HUB1, there is still a background splicing of 5’S site, so we need another parameter b in S-splicing.

Background S-splicing parameter b is mostly related to the ratio of spliceosome and Hub1p-modified spliceosome (Hub1_spliceosome) at equilibrium state. With higher b, L-mRNA and S-mRNA will come closer at equilibrium stat while it influence no-Hub1p situation more than Hub1p situation.

Degradation Rate

Through light intensity we want to convert it to protein concentration as well as calculate its degradation rate, so we made another model to achieve that.

Reaction

Through formula deviation, we obtain the relationship between protein degradation rate and ratio of protein tagged with degradation tags or not.

Since the degradation tags we use is too short when compared to XFP, we simplify our question to:

From experimental fitting curve we got its half-life of our protein 6.88 min. So the degradation rate should be:

While in simulation, we obtained the degradation rate by calculating with [P1_P]/[P2_P]: