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High-throughput Screening for Chemical Modulators of Post-transcriptionally Regulated Genes
Published on: March 3, 2015
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Regulation by 3'-Untranslated Regions.
1Department of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA;
Annual Review of Genetics
|August 31, 2017
Summary
Human messenger RNA 3'-untranslated regions (3'-UTRs) have significantly expanded, suggesting a key role in regulating gene expression and protein interactions, contributing to phenotypic diversity.
Area of Science:
- Molecular Biology
- Genetics
- Genomics
Background:
- 3 -untranslated regions (3 -UTRs) are noncoding mRNA segments.
- Human 3 -UTRs have expanded significantly in length and isoform diversity compared to yeast.
- This expansion suggests a crucial role in higher organism biology.
Purpose of the Study:
- To investigate the regulatory functions of 3 -UTRs in gene expression.
- To explore the role of 3 -UTRs in protein-protein interactions and complex formation.
- To understand the contribution of 3 -UTRs to phenotypic diversity.
Main Methods:
- Analysis of mRNA structures and lengths.
- Investigation of RNA-binding protein interactions with 3 -UTR cis-elements.
- Functional studies on mRNA degradation, translation, and localization.
- Comparative genomics analysis between species.
Main Results:
- 3 -UTRs regulate mRNA fates (degradation, translation, localization).
- 3 -UTRs function as noncoding RNAs and influence protein-protein interactions.
- 3 -UTRs facilitate cotranslational protein complex formation, acting as eukaryotic operons.
- Effector proteins recruited by RNA-binding proteins mediate 3 -UTR functions.
Conclusions:
- 3 -UTRs are critical regulators of gene expression in higher organisms.
- They enable local functions, compartmentalization, and cooperativity.
- 3 -UTRs are key contributors to phenotypic diversity through complex regulatory mechanisms.
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