Developmental Cell
Volume 57, Issue 3, 7 February 2022, Pages 298-309.e9
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Article
Transgenerational inheritance of sexual attractiveness via small RNAs enhances evolvability in C. elegans

https://doi.org/10.1016/j.devcel.2022.01.005Get rights and content
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Highlights

  • Growth at 25°C increases sexual attractiveness of C. elegans hermaphrodites

  • Increased attractiveness transmits transgenerationally via HRDE-1 and small RNAs

  • Attractiveness is associated with sperm defects and small RNAs targeting sperm genes

  • Stress-induced transient epigenetic inheritance enhances mating and can affect evolution

Summary

It is unknown whether transient transgenerational epigenetic responses to environmental challenges affect the process of evolution, which typically unfolds over many generations. Here, we show that in C. elegans, inherited small RNAs control genetic variation by regulating the crucial decision of whether to self-fertilize or outcross. We found that under stressful temperatures, younger hermaphrodites secrete a male-attracting pheromone. Attractiveness transmits transgenerationally to unstressed progeny via heritable small RNAs and the Argonaute Heritable RNAi Deficient-1 (HRDE-1). We identified an endogenous small interfering RNA pathway, enriched in endo-siRNAs that target sperm genes, that transgenerationally regulates sexual attraction, male prevalence, and outcrossing rates. Multigenerational mating competition experiments and mathematical simulations revealed that over generations, animals that inherit attractiveness mate more and their alleles spread in the population. We propose that the sperm serves as a “stress-sensor” that, via small RNA inheritance, promotes outcrossing in challenging environments when increasing genetic variation is advantageous.

Keywords

small RNA inheritance
transgenerational inheritance
epigenetics
non-Mendelian inheritance
genetic variation
C. elegans
sexual attractiveness
sex pheromones
germ granules
evolution
germline

Data and code availability

  • This paper analyses existing, publicly available data. Accession numbers for the datasets are listed in the key resources table. Original western blot images have been deposited at Mendeley and are publicly available as of the date of publication. The DOI is listed in the key resources table.

  • All original code has been deposited at Zenodo and is publicly available as of the date of publication. DOIs are listed in the key resources table.

  • Any additional information required to reanalyse the data reported in this paper is available from the lead contact upon request.

Cited by (0)

4

These authors contributed equally

5

Lead contact