Sammendrag
Synchronization of almost all biological processes is governed by the cyclic pattern of
gene expression in response to the dynamics of the external environment, including
photoperiod. The circadian system is a coordinated feedback loop that is composed of brain
and muscle aryl hydrocarbon receptor nuclear translocator (ARNT)-like (Bmal), Circadian
Locomotor Output Cycles Kaput (Clock), Period (Per) and Cryptochrome (Cry). In Atlantic
cod, photoperiod manipulation is being practiced in delaying precocious sexual maturation
which is a major farming bottleneck. Though promising results have been obtained, the
molecular basis of this phenomenon is largely unknown. This study was conducted to clone
the circadian genes in cod and evaluate their transcriptional oscillation in peripheral tissues
during a maturation cycle, since identifying and characterizing these molecules is necessary
to understand this photic plasticity. Partial sequences of 8 clock genes in cod have been
isolated, namely, bmal1a, bmal1b, clock, clock3, per1, per2, cry1 and cry2. Except for clock,
clock3, cry1and cry2, all genes could only be detected at 50% epiboly, suggesting that most
are zygotic transcripts. Their constitutive expression in almost all tissues indicates that
peripheral circadian oscillators are present in cod. Their expression in two peripheral tissues,
testis and gonads, was quantified and rhythmic oscillation on the transcription was observed
during a maturation cycle.
This study identified the molecular components of the circadian system of Atlantic
cod and revealed how seasonal variation like maturation cycle served as an environmental
cue in their transcription. Further, these environmentally-driven changes provide practical
information in cod aquaculture where photoperiod manipulation is considered as important
strategy in delaying sexual maturation.
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