共 43 条
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.
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页码:743 / U163
页数:10
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