posted on 2020-09-18, 20:47authored byChee Ka
Candice Lam, Kevin Truong
Since cell-based
therapies require the constitutive and stable
expression of therapeutic transgenes, lentiviral infection is commonly
used to integrate gene material regulated by standard constitutive
promoters. Unfortunately, none of the standard or synthetic constitutive
promoters can be easily synthesized at low cost due to the presence
of repeated subsequences. Thus, in this paper, we designed a synthetic
constitutive promoter (named SFCp) that can drive the expression of
fluorescent proteins that subsequently trafficked to intended subcellular
localizations and the expression of synthetic proteins that rewired
the cellular response of Ca2+ to cell morphology changes.
Furthermore, SFCp can be used to avoid sequence homology that can
theoretically result in loss of genetic material by homologous recombination
in tandem constructs. As gene synthesis becomes an indispensable tool
in the arsenal of synthetic biology, it is essential to develop a
toolbox of gene synthesis friendly components for cell engineering
such as constitutive promoters.