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Updated: Sep 15, 2025

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Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution
Published on: January 16, 2017
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Selective RNA sequestration in biomolecular condensates directs cell fate transitions
Patrizia Pessina1,2,3,4, Mika Nevo5,6,7, Junchao Shi8
1Stem Cells and Regenerative Medicine Center, Baylor College of Medicine, Houston, TX, USA.
Biorxiv : the Preprint Server for Biology
|July 14, 2025
Summary
Biomolecular condensates, like P-bodies, control gene expression and cell fate by sequestering specific RNAs. Manipulating these RNA condensates enhances stem cell pluripotency and germ cell development.
Area of Science:
- Cell Biology
- Developmental Biology
- Genetics
Background:
- Biomolecular condensates regulate gene expression via RNA processing and translation.
- The role of RNA condensates in cell fate decisions is not well understood.
Purpose of the Study:
- To investigate the function of RNA condensates (P-bodies) in cell fate specification across vertebrate development.
- To understand the mechanisms of RNA sequestration within P-bodies and their impact on cell fate.
Main Methods:
- Profiling of coding and non-coding transcriptomes within P-bodies from diverse developmental contexts.
- Investigating the role of microRNAs (miRNAs) and AGO2 in RNA sequestration.
- Perturbing P-body assembly and miRNA activity.
Main Results:
- Identified conserved, cell type-specific RNA sequestration in P-bodies, enriched for translationally repressed transcripts.
- Demonstrated that miRNAs direct selective RNA sequestration into P-bodies.
- Showed that modulating P-body assembly or miRNA activity enhances stem cell totipotency and germ cell programming.
Conclusions:
- Established a direct link between biomolecular condensates and cell fate decisions in vertebrates.
- Provided a framework for using condensate biology to expand clinically relevant cell populations.
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