MOLECULAR CLONING OF THE VITELLOGENIN GENE IN THE HARD-LIPPED BARB (Osteochillus hasseltii C.V.) AND PHOTOPERIOD’S EFFECTS ON GENE EXPRESSION
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Photoperiod affects fish reproduction as it regulates activities of the endocrine glands, which produce the hormones needed for geonadal growth and development, gametogenesis, and reproductive cycles. This study aimed to determine the effects of photoperiod on the hard-lipped barb's reproductive performance by exposing the fish to three photoperiod treatments (light hour: L, darks hour: D), namely 14L:10D (control), 8L:16D (short photoperiod) and 18L:6D (long photoperiod), with four aquaria, each containing 9 fish, serving as replicates. The fish were kept under these photoperiods for 8 weeks. Liver activity, the observable variable in the study, was evaluated by measuring vitellogenin gene expression. Normalized data were then subjected to ANOVA, followed by Tukey's range test. The hard-lipped barb's vitellogenin cDNA was found have a 1136 bp sequence and the vitellogenin precursors encoded cDNA comprising 378 amino acids. The vitellogenin gene in each experimental group saw a significant increase on average when exposed to longer photoperiods (P<0.05), and the highest levels of vitellogenin gene expression occurred under long photoperiods (LP, 18 h light:6 h dark). These results indicate that longer photoperiods stimulate and improve the hard-lipped barb's reproductive performance.
Bayyari NIJ, Rodriguez I, Zanuy S, Madrid JA, Sanchez-Vazquez FJ, Kagawa H, ... Carrillo M. 2004. Effect of photoperiod manipulation on the daily rhythms of melatonin and reproductive hormones in caged European sea bass (Dicentrarchus labrax). Gen Comp Endocrinol 136:72-81.
Bhattacharaya S. 1992. Endocrine control and fish reproduction. Curr Sci 63(3):135-9.
Biswas SK, Morita T, Yoshizaki G, Maita M, Takeuchi T. 2005. Control of reproduction in Nile tilapia (Oreochromis niloticus L.) by photoperiod manipulation. Aquaculture 243:229-39.
Bromage NR, Porter MJR, Randall CF. 2001. The environmental regulation of maturation in farmed finfish with special reference to the role of photoperiod and melatonin. Aquaculture 197:63-98.
Cassone VN. 1998. Melatonin’s role in vertebrate circadian rhythms. Chronobiol Int 15:457-73.
Chyb J, Mikolajczyk T, Breton B. 1999. Post-ovulatory secretion of pituitary gonadotropins GtH-I and GtH-II in the rainbow trout (Oncorhynchus mykiss): Regulation by steroids and possible role of non-steroidal gonadal factors. J Endocrinol 63(1):87-97.
Ekstrom P, Meissl H. 1997. The pineal organ of teleost fishes. Rev Fish Biol Fish 7:199-284.
Flack MR, Froehlich J, Bennet AP. 1994. Site-directed mutagenesis defines the individual roles of the glycosylation sites on follicle stimulating hormone. J Biol Chem 269:14015-20.
Hiramatsu N, Matsubara T, Hara A, Donato DM, Hiramatsu K, Denslow ND, Sullivan CV. 2002. Identification, purification, and classification of multiple forms of vitellogenin from white perch (Morone americana). Fish Physiol Biochem 26:355-70.
Kang BJ, Jung JH, Lee JM, Lim SG, Saito H, Kim MH, ... Han CH. 2007. Structural and expression analyses of two vitellogenin genes in the carp, Cyprinus carpio. Comp Biochem Physiol B 148:445-53.
Minniti F, Maisano M, Giannito A, Mauceri A, Sasuolo F. 2007. GtH-I and GtH-II in the pituitary gland of swordfish (Xiphias gladius). Ital J Zool 76:269-78.
Miranda LA, Strussmann CA, Somoza GM. 2008. Effects of light and temperature conditions on the expression of GnRH and GtH genes and levels of plasma steroids in Odontesthes bonariensis females. Fish Physiol Biochem 35:101-8.
Prayogo NA, Wijayanti GE, Murwantoko, Kawaichi M, Astuti P. 2012. Effect of photoperiods on melatonin levels, estradiol levels, and the expression of cGnRH-II and sGnRH genes in hard-lipped barb (Osteochilus hasseltii C.V.). Glob Vet.
Prayogo NA, Wijayanti GE, Sulistyo I, Sukardi P. 2016a. Cloning and expression of cGnRH-II and sGnRH genes in hard-lipped barb (Osteochilus hasseltii C.V.). Biodiversitas.
Prayogo NA, Siregar, Sukardi P. 2016b. The disruptive effect of mercuric chloride (HgCl₂) on gene expression of cGnRH-II, sGnRH, and estradiol levels in silver sharkminnow (Osteochilus hasseltii C.V.). Turk J Fish Aquat Sci 16(2): 1003-9.
Qingbo T, Mazur M, Mellon PL. 2005. The protein kinase C pathway acts through multiple transcription factors to repress gonadotropin-releasing hormone gene expression in hypothalamic GT1–7 neuronal cells. Mol Endocrinol 19(11):2769-79.
Rodriguez I, Carrillo M, Sorbera I, Zohar Y, Zanuy S. 2004. Effects of photoperiod on pituitary levels of three forms of GnRH and reproductive hormones in the male European sea bass (Dicentrarchus labrax L.) during testicular differentiation and first testicular recrudescence. Gen Comp Endocrinol 136:37-48.
Siregar AS, Prayogo NA. 2017. The disruptive effect of mercury chloride (HgCl₂) on gene expression of gonadotrophin hormones and testosterone level in male silver sharkminnow (Osteochilus hasseltii C.V.) (Teleostei: Cyprinidae). European Zoological Journal 84.
Skjæraasen JE, Nilsen T, Kjesbu CS. 2006. Timing and determination of potential fecundity in Atlantic cod (Gadus morhua). Fish Aquat Sci 63:310-20.
Sulistyo I, Fontaine P, Rinchard J, Gardeur JN, Nligaud H, Capdeville B, Kestemont P. 1998. Reproductive cycle and plasma levels of sex steroids in female Eurasian perch (Perca fluviatilis). Aquat Living Resour.
Utoh T, Horie NA, Okamura Y, Yamada S, Tanaka N, Mikawa A, ... Oka HP. 2003. Oogenesis in the common Japanese conger Conger myriaster. Fisheries Sci 69:181-8.
Wang Q, Sham KW, Ogawa S, Li S, Parhar IS, Cheng CH, ... Lin H. 2013. Regulation of the two kiss promoters in goldfish (Carassius auratus) by estrogen via different alpha pathways. Mol Cell Endocrinol 375(1-2):130-9.
Xiong F, Hew CL. 1991. Chinook salmon gonadotropin II ß-subunit gene encodes multiple messenger ribonucleic acids. Can J Zool 69:2572-8.
Yaron Z. 1995. Endocrine control of gametogenesis and spawning induction in the carp. Aquaculture 129:49-73.
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