Enhanced RNA quality control maintains long-term regenerative ability in planarians

Planarians have proficient regenerative abilities that persist undiminished throughout adulthood, mediated by their stem cells (neoblasts). It is unclear how planarians accomplish this, as most animals show age-related declines in health and regeneration. Neoblasts express the conserved RNA regulatory PIWI protein SMEDWI-1, homologs of which are found in germ cells and long-lived cells in other systems. We previously found that loss of SMEDWI-1 from the neoblasts results in accumulation of non-coding and aberrant RNAs. Here, we report that, over time, SMEDWI-1-depleted animals develop defects in wound repair and regeneration, alterations in secreted proteins, and increased intracellular protein aggregation. Our data indicate that these defects result from misassembly of the signal recognition particle (SRP), a ribonucleoprotein (RNP) responsible for co-translational protein secretion that contains a non-coding RNA as a scaffold. In the absence of tight regulation of non-coding RNA, as provided by SMEDWI-1, gradual accumulation of RNAs leads to imbalances in essential cellular machinery such as the SRP, resulting in compromised proteostasis and progressive loss of organismal vigor.

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Publication Details

Journal
Development
Published
2025-09-16
DOI
https://doi.org/10.1242/dev.204762
Citations
1
Primary Topic
Planarian Biology and Electrostimulation
Type
article
Field-Weighted Citation Impact
0.81

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Enhanced RNA quality control maintains long-term regenerative ability in planarians

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Enhanced RNA quality control maintains long-term regenerative ability in planarians

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article en
1 citations

Abstract

Planarians have proficient regenerative abilities that persist undiminished throughout adulthood, mediated by their stem cells (neoblasts). It is unclear how planarians accomplish this, as most animals show age-related declines in health and regeneration. Neoblasts express the conserved RNA regulatory PIWI protein SMEDWI-1, homologs of which are found in germ cells and long-lived cells in other systems. We previously found that loss of SMEDWI-1 from the neoblasts results in accumulation of non-coding and aberrant RNAs. Here, we report that, over time, SMEDWI-1-depleted animals develop defects in wound repair and regeneration, alterations in secreted proteins, and increased intracellular protein aggregation. Our data indicate that these defects result from misassembly of the signal recognition particle (SRP), a ribonucleoprotein (RNP) responsible for co-translational protein secretion that contains a non-coding RNA as a scaffold. In the absence of tight regulation of non-coding RNA, as provided by SMEDWI-1, gradual accumulation of RNAs leads to imbalances in essential cellular machinery such as the SRP, resulting in compromised proteostasis and progressive loss of organismal vigor.

DevelopmentVol. 152(20)
Yale Cancer Center (US), Yale University (US)
Yale University, Vallee Foundation, National Institutes of Health
Openalex Percentile: Top 24%
Planarian Biology and Electrostimulation
0.81
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