Title
Rhythms in clock proteins in the mouse pars tuberalis depend on MT1 melatonin receptor signalling
UMMS Affiliation
Department of Neurobiology; Weaver Lab
Publication Date
2005-12
Document Type
Article
Subjects
ARNTL Transcription Factors; Animals; Basic Helix-Loop-Helix Transcription Factors; CLOCK Proteins; Circadian Rhythm; Feedback; Immunohistochemistry; In Situ Hybridization; Mice; Mice, Knockout; Nerve Tissue Proteins; Pituitary Gland, Posterior; RNA; Receptor, Melatonin, MT1; Signal Transduction; Suprachiasmatic Nucleus; Trans-Activators
Disciplines
Neuroscience and Neurobiology
Abstract
Melatonin provides a rhythmic neuroendocrine output, driven by a central circadian clock that encodes information about phase and length of the night. In the hypophyseal pars tuberalis (PT), melatonin is crucial for rhythmic expression of the clock genes mPer1 and mCry1, and melatonin acting in the PT influences prolactin secretion from the pars distalis. To examine further the possibility of a circadian clockwork functioning in the PT, and the impact of melatonin on this tissue, we assessed circadian clock proteins by immunohistochemistry and compared the diurnal expression in the PT of wild type (WT), and MT1 melatonin receptor-deficient (MT1-/-) mice. While in the PT of WT mice mPER1, mPER2, and mCRY1 showed a pronounced rhythm, mCRY2, CLOCK, and BMAL1 were constitutively present. Despite reported differences in maximal levels and timing of mCry1, mPer1, and mPer2 RNAs, the corresponding protein levels peaked simultaneously during late day, suggesting a codependency for their stabilization and/or nuclear entry. MT1-/- mice had reduced levels of mPER1, mCRY1, CLOCK and BMAL1, consistent with the earlier reported reduction in mRNA expression of these clock genes. Surprisingly, mPER2-immunoreaction was constitutively low, although mPer2 was rhythmically expressed in the PT of MT1-/- mice. This suggests that mPER2 is degraded due to the reduced levels of its stabilizing interaction partners mPER1 and mCRY1. The results show that melatonin, acting through the MT1, determines availability of the circadian proteins mPER1, mPER2 and mCRY1 and thus plays a crucial role in regulating rhythmicity in PT cells.
DOI of Published Version
10.1111/j.1460-9568.2005.04485.x
Source
Eur J Neurosci. 2005 Dec;22(11):2845-54. Link to article on publisher's site
Journal/Book/Conference Title
The European journal of neuroscience
Related Resources
PubMed ID
16324119
Repository Citation
Jilg A, Moek J, Weaver DR, Korf H, Stehle JH, von Gall C. (2005). Rhythms in clock proteins in the mouse pars tuberalis depend on MT1 melatonin receptor signalling. Neurobiology Publications. https://doi.org/10.1111/j.1460-9568.2005.04485.x. Retrieved from https://escholarship.umassmed.edu/neurobiology_pp/68