JOE
HOME HELP CONTACT US SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


DOI: 10.1677/joe.0.1790001

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (54)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lincoln, G.
Right arrow Articles by Loudon, A
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lincoln, G.
Right arrow Articles by Loudon, A
Journal of Endocrinology, Vol 179, Issue 1, 1-13
Copyright © 2003 by Society for Endocrinology


Articles

Clock genes in calendar cells as the basis of annual timekeeping in mammals--a unifying hypothesis

GA Lincoln, H Andersson, and A Loudon


Melatonin-based photoperiod time-measurement and circannual rhythm generation are long-term time-keeping systems used to regulate seasonal cycles in physiology and behaviour in a wide range of mammals including man. We summarise recent evidence that temporal, melatonin-controlled expression of clock genes in specific calendar cells may provide a molecular mechanism for long-term timing. The agranular secretory cells of the pars tuberalis (PT) of the pituitary gland provide a model cell-type because they express a high density of melatonin (mt1) receptors and are implicated in photoperiod/circannual regulation of prolactin secretion and the associated seasonal biological responses. Studies of seasonal breeding hamsters and sheep indicate that circadian clock gene expression in the PT is modulated by photoperiod via the melatonin signal. In the Syrian and Siberian hamster PT, the high amplitude Per1 rhythm associated with dawn is suppressed under short photoperiods, an effect that is mimicked by melatonin treatment. More extensive studies in sheep show that many clock genes (e.g. Bmal1, Clock, Per1, Per2, Cry1 and Cry2) are expressed in the PT, and their expression oscillates through the 24-h light/darkness cycle in a temporal sequence distinct from that in the hypothalamic suprachiasmatic nucleus (central circadian pacemaker). Activation of Per1 occurs in the early light phase (dawn), while activation of Cry1 occurs in the dark phase (dusk), thus photoperiod-induced changes in the relative phase of Per and Cry gene expression acting through PER/CRY protein/protein interaction provide a potential mechanism for decoding the melatonin signal and generating a long-term photoperiodic response. The current challenge is to identify other calendar cells in the central nervous system regulating long-term cycles in reproduction, body weight and other seasonal characteristics and to establish whether clock genes provide a conserved molecular mechanism for long-term timekeeping.


This article has been cited by other articles:


Home page
Biol. Reprod.Home page
H. L Henderson, D. J Hodson, S. J Gregory, J. Townsend, and D. J Tortonese
Gonadotropin-Releasing Hormone Stimulates Prolactin Release from Lactotrophs in Photoperiodic Species Through a Gonadotropin-Independent Mechanism
Biol Reprod, February 1, 2008; 78(2): 370 - 377.
[Abstract] [Full Text] [PDF]


Home page
J ANIM SCIHome page
R. A. Cushman, M. F. Allan, R. M. Thallman, and L. V. Cundiff
Characterization of biological types of cattle (Cycle VII): Influence of postpartum interval and estrous cycle length on fertility
J Anim Sci, September 1, 2007; 85(9): 2156 - 2162.
[Abstract] [Full Text] [PDF]


Home page
Poult. Sci.Home page
J. B. Zawilska, A. Lorenc, M. Berezinska, B. Vivien-Roels, P. Pevet, and D. J. Skene
Photoperiod-Dependent Changes in Melatonin Synthesis in the Turkey Pineal Gland and Retina
Poult. Sci., July 1, 2007; 86(7): 1397 - 1405.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
L. M. Pyter, J. D. Adelson, and R. J. Nelson
Short Days Increase Hypothalamic-Pituitary-Adrenal Axis Responsiveness
Endocrinology, July 1, 2007; 148(7): 3402 - 3409.
[Abstract] [Full Text] [PDF]


Home page
Cold Spring Harb Symp Quant BiolHome page
A.S.I. Loudon, Q.J. Meng, E.S. Maywood, D.A. Bechtold, R.P. Boot-Handford, and M.H. Hastings
The Biology of the Circadian Ck1{epsilon} tau Mutation in Mice and Syrian Hamsters: A Tale of Two Species
Cold Spring Harb Symp Quant Biol, January 1, 2007; 72(0): 261 - 271.
[Abstract] [PDF]


Home page
J. Exp. Biol.Home page
R. Kuntz, C. Kubalek, T. Ruf, F. Tataruch, and W. Arnold
Seasonal adjustment of energy budget in a large wild mammal, the Przewalski horse (Equus ferus przewalskii) I. Energy intake
J. Exp. Biol., November 15, 2006; 209(22): 4557 - 4565.
[Abstract] [Full Text] [PDF]


Home page
J EndocrinolHome page
R. Nogueiras, S. Tovar, S. E Mitchell, P. Barrett, D V. Rayner, C. Dieguez, and L. M Williams
Negative energy balance and leptin regulate neuromedin-U expression in the rat pars tuberalis.
J. Endocrinol., August 1, 2006; 190(2): 545 - 553.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
J. D. Johnston, B. B. Tournier, H. Andersson, M. Masson-Pevet, G. A. Lincoln, and D. G. Hazlerigg
Multiple Effects of Melatonin on Rhythmic Clock Gene Expression in the Mammalian Pars Tuberalis
Endocrinology, February 1, 2006; 147(2): 959 - 965.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
H. Dolatshad, E.A. Campbell, L. O'Hara, E.S. Maywood, M.H. Hastings, and M.H. Johnson
Developmental and reproductive performance in circadian mutant mice
Hum. Reprod., January 1, 2006; 21(1): 68 - 79.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
O. Hibbitt, K. Coward, H. Kubota, N. Prathalingham, W. Holt, K. Kohri, and J. Parrington
In Vivo Gene Transfer by Electroporation Allows Expression of a Fluorescent Transgene in Hamster Testis and Epididymal Sperm and Has No Adverse Effects upon Testicular Integrity or Sperm Quality
Biol Reprod, January 1, 2006; 74(1): 95 - 101.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
G. A. Lincoln, J. D. Johnston, H. Andersson, G. Wagner, and D. G. Hazlerigg
Photorefractoriness in Mammals: Dissociating a Seasonal Timer from the Circadian-Based Photoperiod Response
Endocrinology, September 1, 2005; 146(9): 3782 - 3790.
[Abstract] [Full Text] [PDF]


Home page
J Biol RhythmsHome page
J. Arendt
Melatonin: Characteristics, Concerns, and Prospects
J Biol Rhythms, August 1, 2005; 20(4): 291 - 303.
[Abstract] [PDF]


Home page
ReproductionHome page
F. J P Ebling
The neuroendocrine timing of puberty
Reproduction, June 1, 2005; 129(6): 675 - 683.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
P. G. Giresi, E. J. Stevenson, J. Theilhaber, A. Koncarevic, J. Parkington, R. A. Fielding, and S. C. Kandarian
Identification of a molecular signature of sarcopenia
Physiol Genomics, April 14, 2005; 21(2): 253 - 263.
[Abstract] [Full Text] [PDF]


Home page
J Biol RhythmsHome page
F. Geier, S. Becker-Weimann, A. Kramer, and H. Herzel
Entrainment in a Model of the Mammalian Circadian Oscillator
J Biol Rhythms, February 1, 2005; 20(1): 83 - 93.
[Abstract] [PDF]


Home page
Hum Reprod UpdateHome page
D. J. Kennaway
The role of circadian rhythmicity in reproduction
Hum. Reprod. Update, January 1, 2005; 11(1): 91 - 101.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
C. Teuscher, J. Y. Bunn, P. D. Fillmore, R. J. Butterfield, J. F. Zachary, and E. P. Blankenhorn
Gender, Age, and Season at Immunization Uniquely Influence the Genetic Control of Susceptibility to Histopathological Lesions and Clinical Signs of Experimental Allergic Encephalomyelitis: Implications for the Genetics of Multiple Sclerosis
Am. J. Pathol., November 1, 2004; 165(5): 1593 - 1602.
[Abstract] [Full Text] [PDF]




HOME HELP CONTACT US SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2003 by the Society for Endocrinology.