Light-regulated microRNAs shape dynamic gene expression in the zebrafish circadian clock

PLoS Genet. 2025 Jan 8;21(1):e1011545. doi: 10.1371/journal.pgen.1011545. eCollection 2025 Jan.

Abstract

A key property of the circadian clock is that it is reset by light to remain synchronized with the day-night cycle. An attractive model to explore light input to the circadian clock in vertebrates is the zebrafish. Circadian clocks in zebrafish peripheral tissues and even zebrafish-derived cell lines are entrainable by direct light exposure thus providing unique insight into the function and evolution of light regulatory pathways. Our previous work has revealed that light-induced gene transcription is a key step in the entrainment of the circadian clock as well as enabling the more general adaptation of zebrafish cells to sunlight exposure. However, considerable evidence points to post-transcriptional regulatory mechanisms, notably microRNAs (miRNAs), playing an essential role in shaping dynamic changes in mRNA levels. Therefore, does light directly impact the function of miRNAs? Are there light-regulated miRNAs and if so, which classes of mRNA do they target? To address these questions, we performed a complete sequencing analysis of light-induced changes in the zebrafish transcriptome, encompassing small non-coding RNAs as well as mRNAs. Importantly, we identified sets of light-regulated miRNAs, with many regulatory targets representing light-inducible mRNAs including circadian clock genes and genes involved in redox homeostasis. We subsequently focused on the light-responsive miR-204-3-3p and miR-430a-3p which are predicted to regulate the expression of cryptochrome genes (cry1a and cry1b). Luciferase reporter assays validated the target binding of miR-204-3-3p and miR-430a-3p to the 3'UTRs of cry1a and cry1b, respectively. Furthermore, treatment with mimics and inhibitors of these two miRNAs significantly affected the dynamic expression of their target genes but also other core clock components (clock1a, bmal1b, per1b, per2, per3), as well as the rhythmic locomotor activity of zebrafish larvae. Thus, our identification of light-responsive miRNAs reveals new intricacy in the multi-level regulation of the circadian clockwork by light.

MeSH terms

  • Animals
  • Circadian Clocks* / genetics
  • Circadian Rhythm / genetics
  • Cryptochromes / genetics
  • Cryptochromes / metabolism
  • Gene Expression Regulation* / radiation effects
  • Light*
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Transcriptome
  • Zebrafish Proteins* / genetics
  • Zebrafish Proteins* / metabolism
  • Zebrafish* / genetics

Substances

  • MicroRNAs
  • Zebrafish Proteins
  • Cryptochromes
  • cry1a protein, zebrafish
  • RNA, Messenger

Grants and funding

This study was supported by the National Natural Science Foundation of China (No. 32100376), the National Key Research & Developmental Program of China (No. 2022YFF1001200), the Natural Science Foundation of Gansu Province (No. 23JRRA1040), and the Fundamental Research Funds for the Central Universities (No. lzujbky- 2024-ey09) for HZ, the Deutsche Forschungsgemeinschaft (DFG No. 7420) for AB and the Helmholtz Association funding program, Natural, Artificial and Cognitive Information Processing (NACIP) for NSF and DV. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.