Team:Shenzhen/Project/YAO.Suicider

Original Ideas

Originally, we try to construct such an artificial organelle YAO that YAO receives signal either from biosensor (internal) or from cytoplasm (external) or consequently trigger the host cell apoptosis. However, for YAO are not completed, we use mitochondrion as experiment target. And since we can’t rely on the availability of YAO.Sensor, the idea that Initial signal is given to YAO’s promoter is replaced by that nucleus produce T7 RNAP and transport it into mitochondrion to activate the T7 promoter inside it.

Figure 1. Original ideas.

Final Story

The final story is consist of six parts:

• a. Signal Imitation

After galactose is added to the medium, RNAP can bind to Gal promoter and start transcribe and produce T7 RNAP with signal peptide to mitochondrial matrix. Then T7 RNAP gets into mitochondrial matrix.

• b. Mitochondrion Dysfunction

Once T7 promoter works, DNase is produced to fragmentize the mtDNA which can lead to Respiration difficulty.

• c. Retrograde Signaling from Mitochondrion

Mitochondrial dysfunction can trigger the RTG pathway which is the only known signaling from mt to nucleus.

• d. Holin Production

DLD3 promoter is the only stable downstream promoter relevant with RTG pathway. It can be binded and activated by RTG1/3p which is final production of RTG pathway. Once mitochondrial dysfunction exits, holin with DLD3promoter can be expressed.

• e. Holin Transformation and Destruction

Once holin is produced, it can anchor on the outer membrane of mitochondria and ER, and form dimer with each other. Further more, they can form into a multidimer called dead draft if holin reachs a certain concentration. Dead drafts work like a large pore and release the apoptosis factor: cytochrome C, aif1 and calcium into cytoplasm.

• f. Apoptosis of Host

Apoptosis factor cytochrome C and largely fleeing calcium can trigger the caspase-like pathway. Aif1 such as endo G can.get into nucleus and fragmentate DNA. Finally, host cell is suppressed or even die.

Figure 2. Final stories.

Verification Experiments Design

• For T7 Imitation System

Figure 3. Verify the function of T7 RNAP/Promoter system in cytoplasm. If it works, fluorescence of GFP can be detected in cytoplasm.

Figure 4. Verify the function of T7 RNAP/Promoter system in mitochondrion or unfinished YAO, basing on the availability of signal peptide from cytoplasm to mitochondrial matrix. If it works, fluorescence of mtGFP can be detected in mitochondrion.

• For Retrograde Signaling Part

Because DLD3 is one of the target of RTG pathway of yeast, lowering the basal expression is required.

Figure 5. Verify the basal expression of gene downstream DLD3 promoter. Roughly judge the brightness of GFP, and consequently select a suitable degradation tag for gene downstream DLD3 promotor.

Figure 6. Verify the function of selected degradation tag by using UV as a imitation of DNase produced in mitochondrion that can lead to mitochondrion dysfunction which will drive the gene expression downstream DLD3 promoter through Retrograde signaling from mitochondrion to nucleus.

Figure 7. Verify that holing can make pores on the inner membrane of mitochondrion. This is the alterant of DNase causing mt dysfunction. And it can also produce a membrane without mtDNA.

• For Host Cell Suicide Part



Figure 8. Verify the function of holing in yeast to prove that holing can act as bax/bak protein in human cell as a apoptosis activator. If it works, we can see that between the engineered and versus one, the growthrate curve (OD600) of engineered one tend to be lower than that of versus one.

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