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Updated: May 10, 2026

Metabolic Labeling of Newly Transcribed RNA for High Resolution Gene Expression Profiling of RNA Synthesis, Processing and Decay in Cell Culture
Published on: August 8, 2013
Gene expression is circular: factors for mRNA degradation also foster mRNA synthesis
Gal Haimovich1, Daniel A Medina, Sebastien Z Causse
1Department of Molecular Microbiology, Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 31096, Israel.
Abstract:
Maintaining proper mRNA levels is a key aspect in the regulation of gene expression. The balance between mRNA synthesis and decay determines these levels. We demonstrate that most yeast mRNAs are degraded by the cytoplasmic 5'-to-3' pathway (the "decaysome"), as proposed previously. Unexpectedly, the level of these mRNAs is highly robust to perturbations in this major pathway because defects in various decaysome components lead to transcription downregulation. Moreover, these components shuttle between the cytoplasm and the nucleus, in a manner dependent on proper mRNA degradation. In the nucleus, they associate with chromatin-preferentially ∼30 bp upstream of transcription start-sites-and directly stimulate transcription initiation and elongation. The nuclear role of the decaysome in transcription is linked to its cytoplasmic role in mRNA decay; linkage, in turn, seems to depend on proper shuttling of its components. The gene expression process is therefore circular, whereby the hitherto first and last stages are interconnected.
Insights
Most yeast mRNAs are degraded by the cytoplasmic 5'-to-3' decay pathway. Defects in this pathway surprisingly lead to transcription downregulation, revealing a circular gene expression process.
Area of Science:
- Molecular Biology
- Gene Regulation
- Yeast Genetics
Background:
- Gene expression regulation relies on maintaining precise mRNA levels.
- mRNA levels are determined by the balance between synthesis and decay.
- The cytoplasmic 5 o3 ext{ pathway} (decaysome) is a primary mRNA degradation route.
Purpose of the Study:
- To investigate the robustness of mRNA levels to perturbations in the decaysome pathway.
- To elucidate the mechanisms underlying mRNA level stability.
- To explore potential roles of decaysome components beyond cytoplasmic mRNA decay.
Main Methods:
- Analysis of mRNA levels in yeast strains with defects in decaysome components.
- Investigation of subcellular localization and chromatin association of decaysome proteins.
- Assays to assess the impact of nuclear decaysome component function on transcription.
Main Results:
- mRNA levels are surprisingly robust to decaysome pathway defects.
- Defects in decaysome components trigger downregulation of mRNA transcription.
- Decaysome components shuttle between cytoplasm and nucleus, associating with chromatin near transcription start sites to stimulate initiation and elongation.
Conclusions:
- The decaysome plays a dual role in both mRNA decay and transcription regulation.
- Nuclear functions of the decaysome in transcription are linked to its cytoplasmic role in mRNA decay via protein shuttling.
- Gene expression exhibits a circular regulatory mechanism connecting transcription and mRNA degradation.
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