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Published on: May 9, 2020
mRNA localization as a rheostat to regulate subcellular gene expression
Nevraj S Kejiou1, Alexander F Palazzo1
1Department of Biochemistry, University of Toronto, Toronto, Canada.
Abstract:
It is currently believed that certain messenger RNAs (mRNAs) are localized to distinct subcellular regions to efficiently target their encoded proteins. However, this simplistic model does not explain why in certain scenarios mRNA localization is dispensable for proper protein distribution. In other cases, mRNA localization is accompanied by translational silencing and degradation by the localization machinery. Here we propose that in certain scenarios mRNAs are localized so that they can either be stabilized and translated, or silenced and degraded, in response to the needs of the subcellular locale. In these cases, the localized mRNA, and its cadre of associated factors, act as a rheostat that regulates protein production and/or mRNA stability in response to the needs of its immediate subcellular environment. WIREs RNA 2017, 8:e1416. doi: 10.1002/wrna.1416 For further resources related to this article, please visit the WIREs website.
Insights
Messenger RNAs (mRNAs) are localized to specific cell areas. This localization can control mRNA stability and protein production based on local cellular needs, acting as a regulatory rheostat.
Area of Science:
- Molecular Biology
- Cell Biology
- RNA Biology
Background:
- Current models suggest messenger RNA (mRNA) localization directs protein synthesis to specific subcellular locations.
- However, this model is insufficient to explain cases where mRNA localization is unnecessary or leads to silencing and degradation.
Purpose of the Study:
- To propose a new model where mRNA localization serves a dual role: enabling stabilization and translation, or facilitating silencing and degradation.
- To highlight the function of localized mRNA as a rheostat, adapting protein production and mRNA stability to local cellular requirements.
Main Methods:
- This study is primarily theoretical, proposing a new regulatory model based on existing observations.
- It synthesizes findings from various studies on mRNA localization, translation, and degradation.
Main Results:
- Localized mRNAs, with associated factors, can act as a rheostat, fine-tuning protein production and mRNA stability.
- This rheostat function allows adaptation to the specific needs of the subcellular environment.
Conclusions:
- mRNA localization is not solely for protein targeting but can be a mechanism for dynamic regulation of gene expression.
- Localized mRNAs can be stabilized for translation or silenced and degraded, depending on the cellular context.
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