Abstract
In vertebrates, the circadian rhythm in the activity of serotonin N-acetyltransferase [arylalkylamine N-acetyltransferase (AA-NAT); EC 2.3.1.87] drives the daily rhythm in circulating melatonin. We have discovered that expression of the AA-NAT gene in the rat pineal gland is essentially turned off during the day and turned on at night, resulting in a more than 150-fold rhythm. Expression is regulated by a photoneural system that acts through an adrenergic-cAMP mechanism in pinealocytes, probably involving cAMP response element-binding protein phosphorylation. Turning off AA-NAT expression appears to involve de novo synthesis of a protein that attenuates transcription. A approximately 10-fold night/day rhythm in AA-NAT messenger RNA occurs in the retina, and AA-NAT messenger RNA is also detected at low levels in the brain.
MeSH terms
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Adrenergic beta-Agonists / pharmacology
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Adrenergic beta-Antagonists / pharmacology
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Amino Acid Sequence
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Animals
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Arylamine N-Acetyltransferase / biosynthesis*
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Arylamine N-Acetyltransferase / chemistry
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Brain / enzymology*
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Circadian Rhythm*
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Consensus Sequence
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DNA, Complementary
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Darkness
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Light
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Male
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Melatonin / biosynthesis*
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Molecular Sequence Data
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Organ Specificity
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Phenylephrine / pharmacology
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Pineal Gland / enzymology*
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Pineal Gland / physiology
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Polymerase Chain Reaction
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Propranolol / pharmacology
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RNA, Messenger / analysis
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RNA, Messenger / biosynthesis
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Rats
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Rats, Sprague-Dawley
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Receptors, Adrenergic, beta / physiology
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Sequence Homology, Amino Acid
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Sheep
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Transcription, Genetic*
Substances
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Adrenergic beta-Agonists
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Adrenergic beta-Antagonists
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DNA, Complementary
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RNA, Messenger
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Receptors, Adrenergic, beta
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Phenylephrine
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Propranolol
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Arylamine N-Acetyltransferase
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Melatonin
Associated data
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GENBANK/U29663
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GENBANK/U38306
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GENBANK/U77455