Manipulating nucleosome disfavoring sequences allows fine-tune regulation of gene expression in yeast

被引:158
作者
Raveh-Sadka, Tali [1 ,2 ]
Levo, Michal [1 ,2 ]
Shabi, Uri [3 ]
Shany, Boaz [1 ,2 ]
Keren, Leeat [1 ,2 ]
Lotan-Pompan, Maya [1 ,2 ]
Zeevi, Danny [1 ,2 ]
Sharon, Eilon [1 ,2 ]
Weinberger, Adina [1 ,2 ]
Segal, Eran [1 ,2 ]
机构
[1] Weizmann Inst Sci, Dept Comp Sci & Appl Math, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
[3] Weizmann Inst Sci, Dept Biol Chem, IL-76100 Rehovot, Israel
基金
美国国家卫生研究院; 欧洲研究理事会;
关键词
HISTONE-DNA INTERACTIONS; IN-VIVO; SACCHAROMYCES-CEREVISIAE; SATURATION MUTAGENESIS; PROTEIN EXPRESSION; TRANSCRIPTION; BINDING; PROMOTERS; MECHANISM; GENOME;
D O I
10.1038/ng.2305
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:743 / U163
页数:10
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