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Cryptochrome deficiency enhances transcription but reduces protein levels of pineal Aanat

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/76003

Title: Cryptochrome deficiency enhances transcription but reduces protein levels of pineal Aanat
Authors: Yamanaka, Yujiro Browse this author →KAKEN DB
Yamada, Yoshiko Browse this author →KAKEN DB
Honma, Ken-ichi Browse this author →KAKEN DB
Honma, Sato Browse this author →KAKEN DB
Keywords: Melatonin
Pineal gland
Cryptochrome
Arylalkylamine-N-acetyltransferase
C3H mice
Issue Date: Nov-2018
Publisher: BioScientifica
Journal Title: Journal of molecular endocrinology
Volume: 61
Issue: 4
Start Page: 219
End Page: 229
Publisher DOI: 10.1530/JME-18-0101
PMID: 30328353
Abstract: Cryptochrome (Cry) 1 and 2 are essential for circadian rhythm generation, not only in the suprachiasmatic nucleus, the site of the mammalian master circadian clock, but also in peripheral organs throughout the body. CRY is also known as a repressor of arylalkylamine-N-acetyltransferase (Aanat) transcription; therefore, Cry deficiency is expected to induce constantly high pineal melatonin content. Nevertheless, we previously found that the content was consistently low in melatonin-proficient Cry1 and Cry2 double-deficient mice (Cry1(-/-)/Cry2(-/-)) on C3H background. This study aims to clarify the mechanism underlying this discrepancy. In the Cry1(-/-)/Cry2(-/-) pineal, expression levels of Aanat and clock gene Per1 were consistently high with no circadian fluctuation on the first day in constant darkness, demonstrating that CRY acts in vivo as a repressor of the pineal circadian clock and AANAT. In contrast, the enzyme activity and protein levels of AANAT remained low throughout the day, supporting our previous observation of continuously low melatonin. Thus, effects of Cry deficiency on the responses of beta-adrenergic receptors were examined in cultured pineal glands. Isoproterenol, a beta-adrenergic stimulant, significantly increased melatonin content, although the increase was smaller in Cry1(-/-)/Cry2(-/-) than in WT mice, during both the day and night. However, the increase in cAMP in response to forskolin was similar in both genotypes, indicating that CRY deficiency does not affect the pathway downstream of the beta-adrenergic receptor. These results suggest that a lack of circadian adrenergic input due to CRY deficiency decreases beta-receptor activity and cAMP levels, resulting in consistently low AANAT levels despite abundant Aanat mRNA.
Rights: Disclaimer: this is not the definitive version of record of this article. This manuscript has been accepted for publication in Journal of Molecular Endocrinology, but the version presented here has not yet been copy-edited, formatted or proofed. Consequently, Bioscientifica accepts no responsibility for any errors or omissions it may contain. The definitive version is now freely available at https://doi.org/10.1530/JME-18-0101 2018.
Type: article (author version)
URI: http://hdl.handle.net/2115/76003
Appears in Collections:教育学院・教育学研究院 (Graduate School of Education / Faculty of Education) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 山仲 勇二郎

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