Study / S4V2S1OME2020-06-16
Permutational analysis of Saccharomyces cerevisiae regulatory elements
Namrita Dhillon, Robert Shelansky, Brent Townshend, Miten Jain, Hinrich Boeger et al.
About this study
Gene expression in Saccharomyces cerevisiae is regulated at multiple levels. Genomic and epigenomic mapping of transcription factors and chromatin factors has led to the delineation of various modular regulatory elements—enhancers (upstream activating sequences), core promoters, 5′ untranslated regions (5′ UTRs) and transcription terminators/3′ untranslated regions (3′ UTRs). However, only a few of these elements have been tested in combinations with other elements and the functional interactions between the different modular regulatory elements remain under explored. We describe a simple and rapid approach to build a combinatorial library of regulatory elements and have used this library to study 26 different enhancers, core promoters, 5′ UTRs and transcription terminators/3′ UTRs to estimate the contribution of individual regulatory parts in gene expression. Our combinatorial analysis shows that while enhancers initiate gene expression, core promoters modulate the levels of enhancer-mediated expression and can positively or negatively affect expression from even the strongest enhancers. Principal component analysis (PCA) indicates that enhancer and promoter function can be explained by a single principal component while UTR function involves multiple functional components. The PCA also highlights outliers and suggest differences in mechanisms of regulation by individual elements. Our data also identify numerous regulatory cassettes composed of different individual regulatory elements that exhibit equivalent gene expression levels. These data thus provide a catalog of elements that could in future be used in the design of synthetic regulatory circuits.
Full author list & citation
Namrita Dhillon, Robert Shelansky, Brent Townshend, Miten Jain, Hinrich Boeger, Drew Endy, Rohinton Kamakaka. Permutational analysis of Saccharomyces cerevisiae regulatory elements. 2020-06-16. https://doi.org/10.1093/synbio/ysaa007
Experiments 3
E5BB26PUD
The same 81-construct episomal reporter matrix was measured in glucose-containing medium by flow cytometry across three biological replicates. Per-construct mean fluorescence and dispersion summaries were used to quantify expression and expression noise.
E5L5AXHRP
A directed Golden Gate library of approximately 400,000 episomal yeast reporter plasmids randomly combined 26 endogenous UAS enhancers, 25 cloned core promoters, 26 5′ UTRs and 26 3′ UTR/terminators upstream of mRuby2. W-303 yeast cells were sorted into no-, low-, medium- and high-mRuby2 expression bins, and the cassette identities were recovered by Oxford Nanopore sequencing.
E7EDW0LVF
An arrayed matrix of 81 episomal reporter constructs combined nine UAS enhancers with nine core promoter/5′ UTR modules and a constant PGK1 3′ UTR/terminator. Venus fluorescence was measured with a microtiter plate reader across carbon-source, adenine-depletion, chromatin-factor mutant and temperature-shift conditions.