Promoter Elements Regulate Cytoplasmic mRNA Decay
Author(s) -
Almog Bregman,
Moran Avraham-Kelbert,
Oren Barkai,
Lea Duek,
Adi Guterman,
Mordechai Choder
Publication year - 2011
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2011.12.005
Subject(s) - biology , promoter , messenger rna , cytoplasm , transcription (linguistics) , upstream activating sequence , transcription factor , microbiology and biotechnology , p bodies , gene , gene expression , genetics , translation (biology) , linguistics , philosophy
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.
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