The light-induced transcriptome of the zebrafish pineal gland reveals complex regulation of the circadian clockwork by light

  • Zohar Ben-Moshe
  • , Shahar Alon
  • , Philipp Mracek
  • , Lior Faigenbloom
  • , Adi Tovin
  • , Gad D. Vatine
  • , Eli Eisenberg
  • , Nicholas S. Foulkes
  • , Yoav Gothilf

Research output: Contribution to journalArticlepeer-review

72 Scopus citations

Abstract

Light constitutes a primary signal whereby endogenous circadian clocks are synchronized ('entrained') with the day/night cycle. The molecular mechanisms underlying this vital process are known to require gene activation, yet are incompletely understood. Here, the light-induced transcriptome in the zebrafish central clock organ, the pineal gland, was characterized by messenger RNA (mRNA) sequencing (mRNA-seq) and microarray analyses, resulting in the identification of multiple light-induced mRNAs. Interestingly, a considerable portion of the molecular clock (14 genes) is lightinduced in the pineal gland. Four of these genes, encoding the transcription factors dec1, reverbb1, e4bp4-5 and e4bp4-6, differentially affected clockand light-regulated promoter activation, suggesting that light-input is conveyed to the core clock machinery via diverse mechanisms. Moreover, we show that dec1, as well as the core clock gene per2, is essential for light-entrainment of rhythmic locomotor activity in zebrafish larvae. Additionally, we used microRNA (miRNA) sequencing (miR-seq) and identified pineal-enhanced and light-induced miRNAs. One such miRNA, miR-183, is shown to downregulate e4bp4-6 mRNA through a 30UTR target site, and importantly, to regulate the rhythmic mRNA levels of aanat2, the key enzyme in melatonin synthesis. Together, this genomewide approach and functional characterization of light-induced factors indicate a multi-level regulation of the circadian clockwork by light.

Original languageEnglish
Pages (from-to)3750-3767
Number of pages18
JournalNucleic Acids Research
Volume42
Issue number6
DOIs
StatePublished - Apr 2014
Externally publishedYes

Bibliographical note

Funding Information:
The Israel Science Foundation [1084/12 to Y.G.]; the United States-Israel Binational Science Foundation [2009/290 to Y.G. and E.E.]; the Karlsruhe Institute of Technology (KIT, Germany) through the Helmholtz funding programme: BioInterfaces (to N.S.F.); and a scholarship from the Clore Israel Foundation (to S.A.). Funding for open access charge: The Israel Science Foundation [1084/12], Jerusalem, Israel.

Funding

The Israel Science Foundation [1084/12 to Y.G.]; the United States-Israel Binational Science Foundation [2009/290 to Y.G. and E.E.]; the Karlsruhe Institute of Technology (KIT, Germany) through the Helmholtz funding programme: BioInterfaces (to N.S.F.); and a scholarship from the Clore Israel Foundation (to S.A.). Funding for open access charge: The Israel Science Foundation [1084/12], Jerusalem, Israel.

FundersFunder number
Clore Israel Foundation
Helmholtz
Karlsruhe Institute of Technology
United States-Israel Binational Science Foundation2009/290
Israel Science Foundation1084/12

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