Part:BBa_K4238003
Act1p+NLS-VP16-EL222+CYC1t
This part is responsible for the acceptance of blue light in yeast cells.
EL222 dimerizes under blue light and binds specifically to a particular DNA sequence (C120). NUS Singapore 2022 created Basic Parts by adding the transcription inducers VP16 and NLS to EL222 to promote specific expressions under blue light. We have implemented this part (BBa_K3570021) with the Constitutive promoter ACT1 and the CYC1 terminator in yeast.
Biology
EL222, which consists of a light-oxygen-voltage-sensing (LOV) domain and a DNA binding domain, helix-turn-helix (HTH) domain, is connected to an activation domain (AD), VP16. In the dark, this complex does not bind to DNA because the LOV domain masks the HTH domain. When blue light (450 nm) hits them, the structure of the LOV domain changes, freeing the HTH domain, which binds to each other to form a homodimer that binds to the C120 region in the DNA. The VP16 domain then promotes the expression of the downstream gene [1][2].
Wet lab result
Using BBa_K4238004 as a reporter gene, we tested this parts in plasmid and genome.
Plasmid:
The created sequences were transformed into yeast and assayed. First, the yeast was incubated in the dark for at least 24 hours to reset the photoreceptor and other components. After that, we separated the strains into two groups. The former strain was incubated under blue light with an intensity of 347[μW/cm^2] using the Optocoder, and fluorescence was observed using a microscope 24 hours after the start of the illumination (blue). The latter strain was observed under a microscope after incubation in the dark (dark). Observations were conducted at two conditions: transmitted light (exposure time: 50 ms) and TxR (exposure time: 200 ms). The results are shown in figure 2 and 3 below.
The expression of mCherry was lower when illuminated with blue light, which contradicts the expectation. After we consulted professors, we found out that this might be because the plasmids were lost from the yeast since they were cultured in non-selective medium.
Genome Integration:
The homologous sequences were added upstream and downstream of the EL222 sequence and introduced into the locus YNRCΔ9 on the yeast genome. We generated the sequence of C120-trucCYC1promoter-mCherry-CYC1terminator as a reporter for EL222 by OE-PCR, and homologously recombined it to the genomic locus YMRWΔ15.
The created sequences were transformed into yeast and assayed. First, the yeast was incubated in the dark for at least 24 hours to reset the photoreceptor and other components. After that, we separated the strains into two groups. The former strain was incubated under blue light with an intensity of 420[μW/cm^2] using the Optocoder, and fluorescence was observed using a microscope 3 hours (3h) and 6 hours (6h) after the start of the incubation. The latter strain was observed under a microscope after incubation in the dark(dark). Observations were made at two wavelengths: transmitted light (exposure time: 50 ms) and TxR (exposure time: 200 ms). The results are shown in Figure 5 below.
After 3 hours of blue light irradiation, gene expression was about 3 times higher than that without irradiation, confirming that EL222 was functioning properly. On the other hand, the irradiation for 6 hours did not change the gene expression from the 3-hour time point. This indicates that gene expression had already peaked at 3 hours after irradiation, and that 3 hours of light exposure was sufficient to activate the blue light-dependent promoter.
Reference
[1] Motta-Mena, L. B., Reade, A., Mallory, M. J., Glantz, S., Weiner, O. D., Lynch, K. W., & Gardner, K. H. (2014). An optogenetic gene expression system with rapid activation and deactivation kinetics. Nature chemical biology, 10(3), 196-202. doi: 10.1038/nchembio.1430
[2] "Team:NUS Singapore - 2021.igem.org." https://2021.igem.org/Team:NUS_Singapore (accessed Oct. 09, 2022)
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 801
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 801
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 801
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 801
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 801
- 1000COMPATIBLE WITH RFC[1000]
None |