Circadian clock gene expression in the coral Favia fragum over diel and lunar reproductive cycles.

Natural light cycles synchronize behavioral and physiological cycles over varying time periods in both plants and animals. Many scleractinian corals exhibit diel cycles of polyp expansion and contraction entrained by diel sunlight patterns, and monthly cycles of spawning or planulation that correspo...

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Main Authors: Kenneth D Hoadley, Alina M Szmant, Sonja J Pyott
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3089635?pdf=render
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spelling doaj-828e7ea7b9af4c48b88b4531cfac9b6b2020-11-25T02:15:41ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0165e1975510.1371/journal.pone.0019755Circadian clock gene expression in the coral Favia fragum over diel and lunar reproductive cycles.Kenneth D HoadleyAlina M SzmantSonja J PyottNatural light cycles synchronize behavioral and physiological cycles over varying time periods in both plants and animals. Many scleractinian corals exhibit diel cycles of polyp expansion and contraction entrained by diel sunlight patterns, and monthly cycles of spawning or planulation that correspond to lunar moonlight cycles. The molecular mechanisms for regulating such cycles are poorly understood. In this study, we identified four molecular clock genes (cry1, cry2, clock and cycle) in the scleractinian coral, Favia fragum, and investigated patterns of gene expression hypothesized to be involved in the corals' diel polyp behavior and lunar reproductive cycles. Using quantitative PCR, we measured fluctuations in expression of these clock genes over both diel and monthly spawning timeframes. Additionally, we assayed gene expression and polyp expansion-contraction behavior in experimental corals in normal light:dark (control) or constant dark treatments. Well-defined and reproducible diel patterns in cry1, cry2, and clock expression were observed in both field-collected and the experimental colonies maintained under control light:dark conditions, but no pattern was observed for cycle. Colonies in the control light:dark treatment also displayed diel rhythms of tentacle expansion and contraction. Experimental colonies in the constant dark treatment lost diel patterns in cry1, cry2, and clock expression and displayed a diminished and less synchronous pattern of tentacle expansion and contraction. We observed no pattern in cry1, cry2, clock, or cycle expression correlated with monthly spawning events suggesting these genes are not involved in the entrainment of reproductive cycles to lunar light cycles in F. fragum. Our results suggest a molecular clock mechanism, potentially similar to that in described in fruit flies, exists within F. fragum.http://europepmc.org/articles/PMC3089635?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Kenneth D Hoadley
Alina M Szmant
Sonja J Pyott
spellingShingle Kenneth D Hoadley
Alina M Szmant
Sonja J Pyott
Circadian clock gene expression in the coral Favia fragum over diel and lunar reproductive cycles.
PLoS ONE
author_facet Kenneth D Hoadley
Alina M Szmant
Sonja J Pyott
author_sort Kenneth D Hoadley
title Circadian clock gene expression in the coral Favia fragum over diel and lunar reproductive cycles.
title_short Circadian clock gene expression in the coral Favia fragum over diel and lunar reproductive cycles.
title_full Circadian clock gene expression in the coral Favia fragum over diel and lunar reproductive cycles.
title_fullStr Circadian clock gene expression in the coral Favia fragum over diel and lunar reproductive cycles.
title_full_unstemmed Circadian clock gene expression in the coral Favia fragum over diel and lunar reproductive cycles.
title_sort circadian clock gene expression in the coral favia fragum over diel and lunar reproductive cycles.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Natural light cycles synchronize behavioral and physiological cycles over varying time periods in both plants and animals. Many scleractinian corals exhibit diel cycles of polyp expansion and contraction entrained by diel sunlight patterns, and monthly cycles of spawning or planulation that correspond to lunar moonlight cycles. The molecular mechanisms for regulating such cycles are poorly understood. In this study, we identified four molecular clock genes (cry1, cry2, clock and cycle) in the scleractinian coral, Favia fragum, and investigated patterns of gene expression hypothesized to be involved in the corals' diel polyp behavior and lunar reproductive cycles. Using quantitative PCR, we measured fluctuations in expression of these clock genes over both diel and monthly spawning timeframes. Additionally, we assayed gene expression and polyp expansion-contraction behavior in experimental corals in normal light:dark (control) or constant dark treatments. Well-defined and reproducible diel patterns in cry1, cry2, and clock expression were observed in both field-collected and the experimental colonies maintained under control light:dark conditions, but no pattern was observed for cycle. Colonies in the control light:dark treatment also displayed diel rhythms of tentacle expansion and contraction. Experimental colonies in the constant dark treatment lost diel patterns in cry1, cry2, and clock expression and displayed a diminished and less synchronous pattern of tentacle expansion and contraction. We observed no pattern in cry1, cry2, clock, or cycle expression correlated with monthly spawning events suggesting these genes are not involved in the entrainment of reproductive cycles to lunar light cycles in F. fragum. Our results suggest a molecular clock mechanism, potentially similar to that in described in fruit flies, exists within F. fragum.
url http://europepmc.org/articles/PMC3089635?pdf=render
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