[an error occurred while processing this directive]
en

Relative quantification of mRNA transcription of Cry1 in dif-ferent tissues of sheep in oestrous cycle by real-time quantitative PCR

Expand
  • 1. Animal Husbandry and Veterinary Institute, Xinjiang Academy of Agricultural and Reclamation Science, Shihezi 832000, China; 2. Key Laboratory of sheep Breeding and Development Technology of Xinjiang Production and Construction Crops, Shihezi 832000, China; 3. Agriculture Third Division forty-four regiment Veterinary Station of Xinjiang Production and Construction Corps, Tumushuke City 843900, China

Received date: 2012-07-06

  Revised date: 2012-09-27

  Online published: 2013-01-25

Abstract

Studies have shown that clock gene Cry1 may have important roles in the endocrine process of seasonal reproduction in mammals. In this study, Duolang sheep (non-seasonal reproduction sheep breed) and Chinese Merino (seasonal reproduction sheep breed) were used to determine the expression change of Cry1 in hypothala-mus-pituitary-ovary axis in different stage of estrous cycle by quantitative real-time PCR. The results showed that the Cry1 mRNA was expressed in all tested tissues, in which the expression levels in pineal gland and thyroid gland were higher than in other tissues. As far as different sheep breeds were concerned, the tissue expression profiles of Cry1 at different stage of estrous cycle were broadly similar. Besides hypothalamus, the expression levels of Cry1 in ovary, uterus, pineal gland, pituitary gland, and thyroid gland were all reached to peak in proestrus. The differences of expression change extent for Cry1 in vary, uterus, pineal gland, and pituitary gland in proestrus and oestrus were significant between different sheep breeds. The results suggested that Cry1 may play roles in switching on the estrus and seasonal reproduction.

Cite this article

GAO Lei GAN Shang-Quan YANG Jin-Quan YANG Jian-Bo LIANG Yao-Wei Abdulla Aini·Nula Hong SHEN Min . Relative quantification of mRNA transcription of Cry1 in dif-ferent tissues of sheep in oestrous cycle by real-time quantitative PCR[J]. Hereditas(Beijing), 2013 , 35(1) : 85 -92 . DOI: 10.3724/SP.J.1005.2013.00085

References

[1] King DP, Takahashi JS. Molecular genetics of circadian rhythms in mammals. Annu Rev Neurosci, 2000, 23(1): 713-742.
[2] Ralph MR, Menaker M. A mutation of the circadian system in golden hamsters. Science, 1988, 241(4870): 1225-1227.
[3] Lincoln G, Messager S, Andersson H, Hazlerigg D. Temporal expression of seven clock genes in the suprachiasmatic nucleus and the pars tuberalis of the sheep: evidence for an internal coincidence timer. Proc Natl Acad Sci USA, 2002, 99(21): 13890-13895.
[4] Miyamoto Y, Sancar A. Vitamin B2-based blue-light photoreceptors in the retinohypothalamic tract as the photoactive pigments for setting the circadian clock in mammals. Proc Natl Acad Sci USA, 1998, 95(11): 6097-102.
[5] Lincoln GA, Andersson H, Loudon A. Clock genes in calendar cells as the basis of annual timekeeping in mammals-a unifying hypothesis. J Endocrinol, 2003, 179(1): 1-13.
[6] van der Horst GT, Muijtjens M, Kobayashi K, Takano R, Kanno S, Takao M, de Wit J, Verkerk A, Eker AP, van Leenen D, Buijs R, Bootsma D, Hoeijmakers JH, Yasui A. Mammalian Cry1 and Cry2 are essential for maintenance of circadian rhythms. Nature, 1999, 398(6728): 627-630.
[7] Park K, Kang HM. Cloning and circadian expression of rat Cry1. Mol Cells, 2004, 18(2): 256-260.
[8] Hazlerigg DG, Andersson H, Johnston JD, Lincoln G. Mo-lecular characterization of the long-day response in the Soay sheep, a seasonal mammal. Curr Biol, 2004, 14(4): 334-339.
[9] Vitaterna MH, Selby CP, Todo T, Niwa H, Thompson C, Fruechte EM, Hitomi K, Thresher RJ, Ishikawa T, Miya-zaki J, Takahashi JS, Sancar A. Differential regulation of mammalian period genes and circadian rhythmicity by cryptochromes 1 and 2. Proc Natl Acad Sci USA, 1999, 96(21): 12114-12119.
[10] Shearman LP, Sriram S, Weaver DR, Maywood ES, Chaves I, Zheng BH, Kume K, Lee CC, van der Horst GTJ, Hastings MH, Reppert SM. Interacting molecular loops in the mammalian circadian clock. Science, 2000, 288(5468): 1013-1019.
[11] 高磊, 甘尚权, 杨井泉, 沈敏. 多浪羊发情周期不同阶段阴道细胞变化观察. 黑龙江畜牧兽医, 2012, (21): 35-37.
[12] Mulsant P, Lecerf F, Fabre S, Schibler L, Monget P, Lanneluc I, Pisselet C, Riquet J, Monniaux D, Callebaut I, Cribiu E, Thimonier J, Teyssier J, Bodin L, Cognié Y, Chitour N, Elsen JM. Mutation in bone morphogenetic protein receptor-IB is associated with increased ovulation rate in Booroola Mérino ewes. Proc Natl Acad Sci USA, 2001, 98(9): 5104-5109.
[13] van der Spek PJ, Kobayashi K, Bootsma D, Takao M, Eker APM, Yasui A. Cloning, tissue expression, and mapping of a human photolyase homolog with similarity to plant blue-light receptors. Genomics, 1996, 37(2): 177-182.
[14] Kobayashi K, Kanno SI, Takao M, Yasui A, Smit B, van der Horst GTJ. Characterization of photolyase/blue-light receptor homologs in mouse and human cells. Nucleic Acids Res, 1998, 26 (22): 5086-5092.
[15] Rataiczak CK, Herzoq ED, Muqlia LJ. Clock gene ex-pression in gravid uterus and extra- embryonic tissues during late gestation in the mouse. Reprod Fertil Dey, 2010, 22(5): 743- 750.
[16] Lincoln GA, Andersson H, Hazlerigg D. Clock genes and the long-term regulation of prolactin secretion: evidence for a photoperiod/circannual timer in the pars tuberalis. J Neuroendocrinol, 2003, 15(4): 390-397.
[17] Johnston JD, Tournier BB, Andersson H, Masson-Pévet M, Lincoln GA, Hazlerigg DG. Multiple effects of melatonin on rhythmic clock gene expression in the mammalian pars tuberalis. Endocrinology, 2006, 147(2): 959-965.
[18] Barrett P, Ebling FJP, Schuhler S, Wilson D, Ross AW, Warner A, Jethwa P, Boelen A, Visser TJ, Ozanne DM, Archer ZA, Mercer JG, Mrgan PJ. Hypothalamic thyroid hormone catabolism acts as a gatekeeper for the seasonal control of body weight and reproduction. Endocrinology, 2007, 148 (8): 3608-36
Outlines

/