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Genetically Blocking the Zebrafish Pineal Clock Affects Circadian Behavior.

Authors :
Zohar Ben-Moshe Livne
Shahar Alon
Daniela Vallone
Yared Bayleyen
Adi Tovin
Inbal Shainer
Laura G Nisembaum
Idit Aviram
Sima Smadja-Storz
Michael Fuentes
Jack Falcón
Eli Eisenberg
David C Klein
Harold A Burgess
Nicholas S Foulkes
Yoav Gothilf
Source :
PLoS Genetics, Vol 12, Iss 11, p e1006445 (2016)
Publication Year :
2016
Publisher :
Public Library of Science (PLoS), 2016.

Abstract

The master circadian clock in fish has been considered to reside in the pineal gland. This dogma is challenged, however, by the finding that most zebrafish tissues contain molecular clocks that are directly reset by light. To further examine the role of the pineal gland oscillator in the zebrafish circadian system, we generated a transgenic line in which the molecular clock is selectively blocked in the melatonin-producing cells of the pineal gland by a dominant-negative strategy. As a result, clock-controlled rhythms of melatonin production in the adult pineal gland were disrupted. Moreover, transcriptome analysis revealed that the circadian expression pattern of the majority of clock-controlled genes in the adult pineal gland is abolished. Importantly, circadian rhythms of behavior in zebrafish larvae were affected: rhythms of place preference under constant darkness were eliminated, and rhythms of locomotor activity under constant dark and constant dim light conditions were markedly attenuated. On the other hand, global peripheral molecular oscillators, as measured in whole larvae, were unaffected in this model. In conclusion, characterization of this novel transgenic model provides evidence that the molecular clock in the melatonin-producing cells of the pineal gland plays a key role, possibly as part of a multiple pacemaker system, in modulating circadian rhythms of behavior.

Subjects

Subjects :
Genetics
QH426-470

Details

Language :
English
ISSN :
15537390 and 15537404
Volume :
12
Issue :
11
Database :
Directory of Open Access Journals
Journal :
PLoS Genetics
Publication Type :
Academic Journal
Accession number :
edsdoj.03d4f90eda47e4a4f4962ec6512567
Document Type :
article
Full Text :
https://doi.org/10.1371/journal.pgen.1006445