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Updated: May 15, 2025

Assessment of Selective mRNA Translation in Mammalian Cells by Polysome Profiling
Published on: October 28, 2014
Musashi-dependent mRNA translational activation is mediated through association with the Scd6/Like-sm family member,
Katherine Bronson1,2, Jewel Banik1, Juchan Lim1
1Department of Neuroscience, University of Arkansas for Medical Sciences, 4301 W Markham, Slot 814, Little Rock, AR, 72205, USA.
Abstract:
The Musashi family of sequence-specific RNA binding proteins (Musashi1 and Musashi2) serve a critical role in mediating both physiological and pathological stem cell function in many tissue types by repressing the translation of target mRNAs that encode proteins that promote cell cycle inhibition and cell differentiation. In addition to repression of target mRNAs, we have also identified a role for Musashi proteins in activating the translation of target mRNAs in a context-dependent manner. However, the molecular mechanisms by which Musashi controls target mRNA translational activation have not been fully elucidated. Since Musashi lacks inherent enzymatic activity, its ability to modulate target mRNA translation likely involves recruitment of ancillary proteins to the target mRNA. We have previously identified a number of proteins that specifically associate with Musashi during Xenopus laevis oocyte maturation at a time when Musashi target mRNAs are translationally activated. Here, we demonstrate that one of these proteins, the Scd6/Like-sm family member LSM14B, is a mediator of the Musashi1-dependent mRNA translational activation that is required for oocyte maturation. Unlike previously characterized proteins which interact with the C-terminal domain of Musashi, LSM14B instead associates with the N-terminal RNA recognition motifs. Additionally, we demonstrate that the mammalian Prop1 mRNA, which encodes a key regulator of pituitary development, is translationally activated by Musashi1 in a LSM14B-dependent manner. Our studies support an evolutionarily conserved role for LSM14B in facilitating the ability of Musashi1 to promote target mRNA translation.
Insights
Musashi proteins activate mRNA translation via LSM14B, a novel interaction partner. This mechanism is crucial for oocyte maturation and conserved in mammalian pituitary development.
Area of Science:
- Molecular Biology
- Developmental Biology
- RNA Biology
Background:
- Musashi proteins (Musashi1 and Musashi2) regulate stem cell function by controlling mRNA translation.
- While Musashi proteins typically repress translation, they can also activate it, but the mechanisms are unclear.
- Musashi proteins lack enzymatic activity, suggesting they recruit other proteins to modulate translation.
Purpose of the Study:
- To elucidate the molecular mechanisms of Musashi-mediated mRNA translational activation.
- To identify proteins that mediate Musashi1-dependent translational activation.
- To investigate the role of LSM14B in Musashi1-mediated translational activation.
Main Methods:
- Protein association studies during Xenopus laevis oocyte maturation.
- Investigating the interaction domain between Musashi1 and LSM14B.
- Analyzing the effect of Musashi1 and LSM14B on Prop1 mRNA translation in mammals.
Main Results:
- LSM14B, a Scd6/Like-sm family member, mediates Musashi1-dependent mRNA translational activation essential for oocyte maturation.
- LSM14B interacts with the N-terminal RNA recognition motifs of Musashi, distinct from other known interaction partners.
- Musashi1-dependent and LSM14B-mediated translational activation of mammalian Prop1 mRNA, a pituitary development regulator, was demonstrated.
Conclusions:
- LSM14B is a key mediator of Musashi1-dependent mRNA translational activation.
- The interaction between Musashi1 and LSM14B is crucial for oocyte maturation.
- This mechanism of translational control by Musashi1 and LSM14B is evolutionarily conserved and relevant to mammalian development.
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