TY - JOUR
T1 - Manipulating nucleosome disfavoring sequences allows fine-tune regulation of gene expression in yeast
AU - Raveh - Sadka, - Sadka, Tali
AU - Levo, Michal
AU - Shabi, Uri
AU - Shany, Boaz
AU - Keren, Leeat
AU - Lotan-Pompan, Maya
AU - Zeevi, Danny
AU - Sharon, Eilon
AU - Weinberger, Adina
AU - Segal, Eran
N1 - European Research Council (ERC); US National Institutes of Health (NIH); Azrieli FoundationWe wish to dedicate this paper to Jon Widom who inspired and assisted us greatly throughout this project. This work was supported by grants from the European Research Council (ERC) and the US National Institutes of Health (NIH) to E. Segal. E. Segal is the incumbent of the Soretta and Henry Shapiro career development chair. T.R.-S. and M.L. thank the Azrieli Foundation for the award of an Azrieli Fellowship. We thank G. Hornung for his help with the analysis of flow cytometry measurements and E. Mochly for his help with the preparation of Supplementary Figure 9.
PY - 2012/7
Y1 - 2012/7
N2 - Understanding how precise control of gene expression is specified within regulatory DNA sequences is a key challenge with far-reaching implications. Many studies have focused on the regulatory role of transcription factor-binding sites. Here, we explore the transcriptional effects of different elements, nucleosome-disfavoring sequences and, specifically, poly(dA:dT) tracts that are highly prevalent in eukaryotic promoters. By measuring promoter activity for a large-scale promoter library, designed with systematic manipulations to the properties and spatial arrangement of poly(dA:dT) tracts, we show that these tracts significantly and causally affect transcription. We show that manipulating these elements offers a general genetic mechanism, applicable to promoters regulated by different transcription factors, for tuning expression in a predictable manner, with resolution that can be even finer than that attained by altering transcription factor sites. Overall, our results advance the understanding of the regulatory code and suggest a potential mechanism by which promoters yielding prespecified expression patterns can be designed.
AB - Understanding how precise control of gene expression is specified within regulatory DNA sequences is a key challenge with far-reaching implications. Many studies have focused on the regulatory role of transcription factor-binding sites. Here, we explore the transcriptional effects of different elements, nucleosome-disfavoring sequences and, specifically, poly(dA:dT) tracts that are highly prevalent in eukaryotic promoters. By measuring promoter activity for a large-scale promoter library, designed with systematic manipulations to the properties and spatial arrangement of poly(dA:dT) tracts, we show that these tracts significantly and causally affect transcription. We show that manipulating these elements offers a general genetic mechanism, applicable to promoters regulated by different transcription factors, for tuning expression in a predictable manner, with resolution that can be even finer than that attained by altering transcription factor sites. Overall, our results advance the understanding of the regulatory code and suggest a potential mechanism by which promoters yielding prespecified expression patterns can be designed.
UR - http://www.scopus.com/inward/record.url?scp=84862984796&partnerID=8YFLogxK
U2 - https://doi.org/10.1038/ng.2305
DO - https://doi.org/10.1038/ng.2305
M3 - مقالة
SN - 1061-4036
VL - 44
SP - 743
EP - 750
JO - Nature Genetics
JF - Nature Genetics
IS - 7
ER -