Abe T, Suzuki T, Unno M, Tokui T, Ito S. Thyroid hormone transporters: recent advances. Trends Endocrinol Metab. 2002;13:215–20.
Bailey MJ, Cassone VM. Melanopsin expression in the chick retina and pineal gland. Brain Res Mol Brain Res. 2005;134:345–8.
Balsalobre A. Clock genes in mammalian peripheral tissues. Cell Tissue Res. 2002;309:193–9.
Benoit J. Le role des yeux dans l’action stimulante de la lumière sur le developpement testiculaire chez le canard. C R Soc Biol (Paris). 1935;118:669–71.
Bernal J. Action of thyroid hormone in brain. J Endocrinol Invest. 2002;25:268–88.
Berson DM, Dunn FA, Takao M. Phototransduction by retinal ganglion cells that set the circadian clock. Science. 2002;295:1070–3.
Chaurasia SS, Rollag MD, Jiang G, Hayes WP, Haque R, Natesan A, Zatz M, Tosini G, Liu C, Korf HW, Iuvone PM, Provencio I. Molecular cloning, localization and circadian expression of chicken melanopsin (Opn4): differential regulation of expression in pineal and retinal cell types. J Neurochem. 2005;92:158–70.
Davies DT, Follett BK. The neuroendocrine control of gonadotrophin release in the Japanese quail. II. The role of the anterior hypothalamus. Proc R Soc Lond B. 1975;191:303–15.
Davies WI, Turton M, Peirson SN, Follett BK, Halford S, Garcia-Fernandez JM, Sharp PJ, Hankins MW, Foster RG. Vertebrate ancient opsin photopigment spectra and the avian photoperiodic response. Biol Lett. 2012;8:291–4.
Dawson A, King VM, Bentley GE, Ball GF. Photoperiodic control of seasonality in birds. J Biol Rhythms. 2001;16:365–80.
Ebihara S, Kawamura H. The role of the pineal organ and the suprachiasmatic nucleus in the control of circadian locomotor rhythms in the Java sparrow, Padda oryzivora. J Comp Physiol A. 1981;141:207–14.
Follett BK, Maung SL. Rate of testicular maturation, in relation to gonadotrophin and testosterone levels, in quail exposed to various artificial photoperiods and to natural daylengths. J Endocrinol. 1978;78:267–80.
Follett BK, Sharp PJ. Circadian rhythmicity in photoperiodically induced gonadotrophin release and gonadal growth in the quail. Nature. 1969;223:968–71.
Follett BK, King VM, Meddle SL. Rhythms and photoperiodism in birds. In: Lumsden PJ, Miller AJ, editors. Biological rhythms and photoperiodism in plants. Oxford: Biostatistics Scientific; 1998. p. 231–42.
Foster RG, Follett BK. The involvement of a rhodopsin-like photopigment in the photoperiodic response of the Japanese quail. J Comp Physiol A. 1985;157:519–28.
Foster RG, Follett BK, Lythgoe JN. Rhodopsin-like sensitivity of extra-retinal photoreceptors mediating the photoperiodic response in quail. Nature. 1985;313:50–2.
Foster RG, Korf HW, Schalken JJ. Immunocytochemical markers revealing retinal and pineal but not hypothalamic photoreceptor systems in the Japanese quail. Cell Tissue Res. 1987;248:161–7.
Furlow JD, Neff ES. A developmental switch induced by thyroid hormone: Xenopus laevis metamorphosis. Trends Endocrionol Metab. 2006;17:40–7.
Garner WW, Allard HA. Effect of the relative length of day and night and other factors of the environment on growth and reproduction in plants. J Agric Res. 1920;18:553–606.
Gwinner E, Hau H, Heigl S. Melatonin: generation and modification of avian circadian rhythms. Brain Res Bull. 1997;44:439–44.
Hagenbuch B, Meier PJ. Organic anion transporting polypeptides of the OATP/SLC21 family: phylogenetic classification as OATP/SLCO superfamily, new nomenclature and molecular/functional properties. Eur J Physiol. 2004;447:653–65.
Hahn TP, MacDougall-Shackleton SA. Adaptive specialization, conditional plasticity and phylogenetic history in the reproductive cue response systems of birds. Philos Trans R Soc B. 2008;363:267–86.
Halford S, Pires SS, Turton M, Zheng L, Gonzalez-Menendez I, Davies WL, Peirson SN, Garcia-Fernandez JM, Hankins MW, Foster RG. VA opsin-based photoreceptors in the hypothalamus of birds. Curr Biol. 2009;19:1396–402.
Homma K, Ohta M, Sakakibara Y. Photoinducible phase of the Japanese quail detected by direct stimulation of the brain. In: Suda M, Hayaishi O, Nakagawa H, editors. Biological rhythms and their central mechanism. Amsterdam: Elsevier; 1979. p. 85–94.
Ikegami K, Katou Y, Higashi K, Yoshimura T. Localization of circadian clock protein BMAL1 in the photoperiodic signal transduction machinery in Japanese quail. J Comp Neurol. 2009;517:397–404.
Ikegami K, Liao XH, Hoshino Y, Ono H, Ota W, Ito Y, Nishiwaki-Ohkawa T, Sato C, Kitajima K, Iigo M, Shigeyoshi Y, Yamada M, Murata Y, Refetoff S, Yoshimura T. Tissue-specific post-translational modification allows functional targeting of thyrotropin. Cell Rep. 2014;9:1–9.
Ikegami K, Atsumi Y, Yorinaga E, Ono H, Murayama I, Nakane Y, Ota W, Arai N, Tega A, Iigo M, Darras VM, Tsutsui K, Hayashi Y, Yoshida S, Yoshimura T. Low temperature-induced circulating triiodothyronine accelerates seasonal testicular regression. Endocrinology. 2015;156:647–59.
Juss TS, Meddle SL, Servant RS, King VM. Melatonin and photoperiodic time measurement in Japanese quail (Coturnix coturnix japonica). Proc R Soc Lond B Biol Sci. 1993;254:21–8.
Kang SW, Leclerc B, Kosonsiriluk S, Mauro LJ, Iwasawa A, El Halawani ME. Melanopsin expression in dopamine–melatonin neurons of the premammillary nucleus of the hypothalamus and seasonal reproduction in birds. Neuroscience. 2010;170:200–13.
Konishi H, Foster RG, Follett BK. Evidence for a daily rhythmicity in the acute release of LH in response to electrical stimulation in the Japanese quail. J Comp Physiol A Sens Neural Behav Physiol. 1987;161:315–9.
Lamb TD. Evolution of vertebrate retinal photoreception. Phil Trans R Soc B. 2009;364:2911–24.
Lofts B, Murton RK, Westwood NJ. Photoresponses of the Woodpigeon Columba palumbus in relation to the breeding season. Ibis. 1967;109:338–51.
MacDougall-Shackleton SA, Stevenson TJ, Watts HE, Pereyra ME, Hahn TP. The evolution of photoperiod response systems and seasonal GnRH plasticity in birds. Integr Comp Biol. 2009;49:580–9.
Marcovitch S. Plant lice and light exposure. Science. 1923;58:537–8.
Max M, McKinnon PJ, Seidenman KJ, Barrett RK, Applebury ML, Takahashi JS, Margolskee RF. Pineal opsin: a nonvisual opsin expressed in chick pineal. Science. 1995;267:1502–6.
Meddle SL, Follett BK. Photoperiodically driven changes in Fos expression within the basal tuberal hypothalamus and median eminence of Japanese quail. J Neurosci. 1997;17:8909–18.
Menaker M. Extraretinal light perception in the sparrow. I. Entrainment of the biological clock. Proc Natl Acad Sci U S A. 1968;59:414–21.
Menaker M, Roberts R, Elliott J, Underwood H. Extraretinal light perception in the sparrow. III. The eyes do not participate in photoperiodic photoreception. Proc Natl Acad Sci U S A. 1970;67:320–5.
Nakane Y, Yoshimura T. Universality and diversity in the signal transduction pathway that regulates seasonal reproduction in vertebrates. Front Neurosci. 2014;8:115.
Nakane Y, Ikegami K, Ono H, Yamamoto N, Yoshida S, Hirunagi K, Ebihara S, Kubo Y, Yoshimura T. A mammalian neural tissue opsin (Opsin 5) is a deep brain photoreceptor in birds. Proc Natl Acad Sci U S A. 2010;107:15264–8.
Nakane Y, Ikegami K, Iigo M, Ono H, Takeda K, Takahashi D, Uesaka M, Kimijima M, Hashimoto R, Arai N, Suga T, Kosuge K, Abe T, Maeda R, Senga T, Amiya N, Azuma T, Amano M, Abe H, Yamamoto N, Yoshimura T. The saccus vasculosus of fish is a sensor of seasonal changes in day length. Nat Commun. 2013;4:2108.
Nakane Y, Shimmura T, Abe H, Yoshimura T. Intrisic photosensitivity of a deep brain photoreceptor. Curr Biol. 2014;24:R596–7.
Nakao N, Takagi T, Iigo M, Tsukamoto T, Yasuo S, Masuda T, Yanagisawa T, Ebihara S, Yoshimura T. Possible involvement of organic anion transporting polypeptide 1c1 in the photoperiodic response of gonads in birds. Endocrinology. 2006;147:1067–73.
Nakao N, Ono H, Yamamura T, Anraku T, Takagi T, Higashi K, Yasuo S, Katou Y, Kageyama S, Uno Y, Kasukawa T, Iigo M, Sharp PJ, Iwasawa A, Suzuki Y, Sugano S, Niimi T, Mizutani M, Namikawa T, Ebihara S, Ueda HR, Yoshimura T. Thyrotrophin in the pars tuberalis triggers photoperiodic response. Nature. 2008;452:317–22.
Nicholls TJ, Follett BK, Robinson JE. A photoperiodic response in gonadectomized Japanese quail exposed to a single long day. J Endocrinol. 1983;97:121–6.
Nicholls TJ, Goldsmith AR, Dawson A. Photorefractoriness in birds and comparison with mammals. Physiol Rev. 1988;68:133–76.
Oishi T, Konishi T. Effects of photoperiod and temperature on testicular and thyroid activity of the Japanese quail. Gen Comp Endocrinol. 1978;36:250–4.
Okano T, Yoshizawa T, Fukada Y. Pinopsin is a chicken pineal photoreceptive molecule. Nature. 1994;372:94–7.
Oliver J, Bayle JD. Brain photoreceptors for the photoinduced testicular response in birds. Experientia. 1982;38:1020–9.
Ono H, Hoshino Y, Yasuo S, Watanabe M, Nakane Y, Murai A, Ebihara S, Korf HW, Yoshimura T. Involvement of thyrotropin in photoperiodic signal transduction in mice. Proc Natl Acad Sci U S A. 2008;105:18238–42.
Ono H, Nakao N, Yamamura T, Kinoshita K, Mizutami M, Namikawa T, Iigo M, Ebihara S, Yoshimura T. Red jungle fowl (Gallus gallus) as a model for studying the molecular mechanism of seasonal reproduction. Anim Sci J. 2009;80:328–32.
Pearce EN. Thyroid hormone and obesity. Curr Opin Endocrinol Diabetes Obes. 2012;19:408–13.
Perfito N, Jeong SY, Silverin B, Calisi RM, Bentley GE, Hau M. Anticipating spring: wild populations of great tits (Parus major) differ in expression of key genes for photoperiodic time measurement. PLoS One. 2012;7:e34997.
Prevot V, Croix D, Bouret S, Dutoit S, Tramu G, Stefano GB, Beauvillain JC. Definitive evidence for the existence of morphological plasticity in the external zone of the median eminence during the rat estrous cycle: implication of neuro-glio-endothelial interactions in gonadotropin-releasing hormone release. Neuroscience. 1999;94:809–19.
Reppert SM, Weaver DR. Coordination of circadian timing in mammals. Nature. 2002;418:935–41.
Rowan W. Relation of light to bird migration and developmental changes. Nature. 1925;115:494–5.
Sharp PJ, Follett BK. The effect of hypothalamic lesions on gonadotrophin release in Japanese quail (Coturnix coturnix japonica). Neuroendocrinol. 1969;5:205–18.
Silva JE. Thermogenic mechanisms and their hormonal regulation. Physiol Rev. 2006;86:435–64.
Silver R, Witkovsky P, Horvath P, Alones V, Barnstable CJ, Lehman MN. Coexpression of opsin- and VIP-like-immunoreactivity in CSF-contacting neurons of the avian brain. Cell Tissue Res. 1988;253:189–98.
Siopes TD, Wilson WO. Extraocular modification of photoreception in intact and pinealectomized coturnix. Poult Sci. 1974;53:2035–41.
Steele CT, Zivkovic BD, Siopes T, Underwood H. Ocular clocks are tightly coupled and act as pacemakers in the circadian system of Japanese quail. Am J Physiol Regul Integr Comp Physiol. 2003;284:R208–18.
Stevenson TJ, Ball GF. Disruption of neuropsin mRNA expression via RNA interference facilitates the photoinduced increase in thyrotropin-stimulating subunit β in birds. Eur J Neurosci. 2012;36:2859–65.
Stevenson TJ, Hahn TP, MacDougall-Shackleton SA, Ball GF. Gonadotropin-releasing hormone plasticity: a comparative perspective. Front Neuroendocrionol. 2012;33:287–300.
Takahashi JS, Menaker M. Role of the suprachiasmatic nucleus in the circadian system of the house sparrow. J Neurosci. 1982;2:815–28.
Tarttelin EE, Bellingham J, Hankins MW, Foster RG, Lucas RJ. Neuropsin (Opn5): a novel opsin identified in mammalian neural tissue. FEBS Lett. 2003;554:410–6.
Tomonari S, Takagi A, Akamatsu S, Noji S, Ohuchi H. A non-canonical photopigment, melanopsin, is expressed in the differentiating ganglion, horizontal, and bipolar cells of the chicken retina. Dev Dyn. 2005;234:783–90.
Tomonari S, Takagi A, Noji S, Ohuchi H. Expression pattern of the melanopsin-like (cOpn4m) and VA opsin-like genes in the developing chicken retina and neural tissues. Gene Expr Patterns. 2007;7:746–53.
Tsutsui K, Saigoh E, Ukena K, Teranishi H, Fujisawa Y, Kikuchi M, Ishii S, Sharp PJ. A novel avian hypothalamic peptide inhibiting gonadotropin release. Biochem Biophys Res Commun. 2000;275:661–7.
Ubuka T, Bentley GE, Ukena K, Wingfield JC, Tsutsui K. Melatonin induces the expression of gonadotropin-inhibitory hormone in the avian brain. Proc Natl Acad Sci U S A. 2005;102:3052–7.
Ubuka T, Ukena K, Sharp PJ, Bentley GE, Tsutsui K. Gonadotropin-inhibitory hormone inhibits gonadal development and maintenance by decreasing gonadotropin synthesis and release in male quail. Endocrinology. 2006;147:1187–94.
Vigh B, Vigh-Teichmann I. Actual problems of the cerebrospinal fluid-contacting neurons. Microsc Res Tech. 1998;41:57–83.
von Frisch K. Beitrage zur Physiologie der Pigmentzellen in der Fischhaut. Pfluger’s Archiv fűr die Gesamte Physiologie des Menschen und der Tiere. 1911;138:319–87.
Wada M. Low temperature and short days together induce thyroid activation and suppression of LH release in Japanese quail. Gen Comp Endocrinol. 1993;90:355–63.
Wada Y, Okano T, Adachi A, Ebihara S, Fukada Y. Identification of rhodopsin in the pigeon deep brain. FEBS Lett. 1998;424:53–6.
Watanabe T, Yamamura T, Watanabe M, Yasuo S, Nakao N, Dawson A, Ebihara S, Yoshimura T. Hypothalamic expression of thyroid hormone-activating and -inactivating enzyme genes in relation to photorefractoriness in birds and mammals. Am J Physiol Regul Integr Comp Physiol. 2007;292:R568–72.
Waung JA, Bassett JH, Williams GR. Thyroid hormone metabolism in skeletal development and adult bone maintenance. Trends Endocrinol Metab. 2012;23:155–62.
Yamamura T, Hirunagi K, Ebihara S, Yoshimura T. Seasonal morphological changes in the neuro-glial interaction between gonadotropin-releasing hormone nerve terminals and glial endfeet in Japanese quail. Endocrinology. 2004;145:4264–7.
Yamamura T, Yasuo S, Hirunagi K, Ebihara S, Yoshimura T. T3 implantation mimics photoperiodically reduced encasement of nerve terminals by glial processes in the median eminence of Japanese quail. Cell Tissue Res. 2006;324:175–9.
Yamashita T, Ohuchi H, Tomonari S, Ikeda K, Sakai K, Shichida Y. Opn5 is a UV-sensitive bistable pigment that couples with Gi subtype of G protein. Proc Natl Acad Sci U S A. 2010;107:22084–9.
Yamazaki S, Numano R, Abe M, Hida A, Takahashi R, Ueda M, Block GD, Sakaki Y, Menaker M, Tei H. Resetting central and peripheral circadian oscillators in transgenic rats. Science. 2000;288:682–5.
Yasuo S, Watanabe M, Okabayashi N, Ebihara S, Yoshimura T. Circadian clock genes and photoperiodism: comprehensive analysis of clock gene expression in the mediobasal hypothalamus, the suprachiasmatic nucleus, and the pineal gland of Japanese quail under various light schedules. Endocrinology. 2003;144:3742–8.
Yasuo S, Watanabe M, Nakao N, Takagi T, Follett BK, Ebihara S, Yoshimura T. The reciprocal switching of two thyroid hormone-activating and -inactivating enzyme genes is involved in the photoperiodic gonadal response of Japanese quail. Endocrinology. 2005;146:2551–4.
Yasuo S, Yoshimura T, Ebihara S, Kolf HW. Melatonin transmits photoperiodic signals through the MT1 melatonin receptor. J Neurosci. 2009;29:2885–9.
Yoshimura T, Yasuo S, Suzuki Y, Makino E, Yokota Y, Ebihara S. Identification of the suprachiasmatic nucleus in birds. Am J Physiol Regul Integr Comp Physiol. 2001;280:R1185–9.
Yoshimura T, Yasuo S, Watanabe M, Iigo M, Yamamura T, Hirunagi K, Ebihara S. Light-induced hormone conversion of T4 to T3 regulates photoperiodic response of gonads in birds. Nature. 2003;426:178–81.
Young MW, Kay SA. Time zones: a comparative genetics of circadian clocks. Nat Rev Genet. 2001;2:702–15.