Part:BBa_K3748011
pPAB1
S.cerevisiae medium strenght promoter.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Team Estonia_TUIT characterization of BBa_K3748011 (pPAB1)
Constitutive pPAB1 (Lee et al., 2015) regulates the expression of an essential gene encoding for poly(A) binding protein, which is involved in the regulation of poly(A) tail length. Pab1 is localized to the nucleus and cytoplasm. It was shown that modulation of Pab1 levels could improve cell fitness under stress conditions (Martani et al., 2015).
We quantified the expression driven by the PAB1 promoter using fluorescent proteins as reporter genes. The expression cassettes were integrated into the yeast genome, and the fluorescence of the reporter proteins was monitored by quantitative time-lapse microscopy. The fluorescence levels were compared to the cell background fluorescence of the control DOM90 strain, which does not express any fluorescent proteins.
pPAB1 promoter showed a constitutive level of Venus fluorescence during the experiment, confirming that it is a constitutive promoter. Compared to the background fluorescence of the DOM90 strain, pPAB1 showed a 19-fold higher expression level, and pREV1 demonstrated a five-fold higher level of fluorescence intensity (figure 1).
Analyzed constitutive promoter can be recommended when constant moderate (pPAB1 promoter) expression of a target gene is required.
References:
- Lee, M. E., DeLoache, W. C., Cervantes, B., & Dueber, J. E. (2015). A Highly Characterized Yeast Toolkit for Modular, Multipart Assembly. ACS Synthetic Biology, 4(9), 975–986. https://doi.org/10.1021/SB500366V/SUPPL_FILE/SB500366V_SI_002.ZIP
- Martani, F., Marano, F., Bertacchi, S., Porro, D., & Branduardi, P. (2015). The Saccharomyces cerevisiae poly(A) binding protein Pab1 as a target for eliciting stress-tolerant phenotypes. Scientific Reports, 5, 18318. https://doi.org/10.1038/SREP18318
None |