Promoter Elements Regulate Cytoplasmic mRNA Decay

被引:135
作者
Bregman, Almog [1 ]
Avraham-Kelbert, Moran [1 ]
Barkai, Oren [1 ]
Duek, Lea [1 ]
Guterman, Adi [1 ]
Choder, Mordechai [1 ]
机构
[1] Technion Israel Inst Technol, Dept Mol Microbiol, Rappaport Fac Med, IL-31096 Haifa, Israel
基金
以色列科学基金会;
关键词
GENE-EXPRESSION; TRANSCRIPTIONAL ACTIVATION; CODING REGION; YEAST; PROTEIN; DEGRADATION; TURNOVER; TRANSLATION; STABILITY; SUBUNIT;
D O I
10.1016/j.cell.2011.12.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Promoters are DNA elements that enable transcription and its regulation by trans-acting factors. Here, we demonstrate that yeast promoters can also regulate mRNA decay after the mRNA leaves the nucleus. A conventional yeast promoter consists of a core element and an upstream activating sequence (UAS). We find that changing UASs of a reporter gene without altering the transcript sequence affects the transcript's decay kinetics. A short cis element, comprising two Rap1p-binding sites, and Rap1p itself, are necessary and sufficient to induce enhanced decay of the reporter mRNA. Furthermore, Rap1p stimulates both the synthesis and the decay of a specific population of endogenous mRNAs. We propose that Rap1p association with target promoter in the nucleus affects the composition of the exported mRNP, which in turn regulates mRNA decay in the cytoplasm. Thus, promoters can play key roles in determining mRNA levels and have the capacity to coordinate rates of mRNA synthesis and decay.
引用
收藏
页码:1473 / 1483
页数:11
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