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Annotated Bibliography of Key Works<br />

1. Selvaraj S., H. Kitano, Y. Fujinaga, H. Ohga, M. Yoneda, A. Yamaguchi, A. Shimizu, <strong>and</strong> M.<br />

Matsuyama. 2010. Molecular characterization, tissue distribution, <strong>and</strong> mRNA expression<br />

profiles of two Kiss genes in the adult male <strong>and</strong> female chub mackerel (Scomber japonicus)<br />

during different gonadal stages. Gen. Comp. Endocrinol. DOI:10.1016/j.ygcen.2010.07.011.<br />

The full-length cDNAs of Kiss1 <strong>and</strong> Kiss2 in the chub mackerel were cloned <strong>and</strong> sequenced.<br />

Chub mackerel K iss1 <strong>and</strong> Kiss2 cDNAs encode 105 <strong>and</strong> 123 amino acids, respectively. A<br />

comparison of the deduced amino acid sequences of chub mackerel Kiss1 <strong>and</strong> Kiss2 with those of<br />

other vertebrate species showed a high degree of conservation only in the kisspeptin-10 region<br />

(Kp-10). The Kp-10 of chub mackerel Kiss1 (YNFNSFGLRY) <strong>and</strong> Kiss2 (FNFNPFGLRF)<br />

showed variations at three amino acids. The mRNA expression profiles of Kiss1 <strong>and</strong> Kiss2 in the<br />

brain, pituitary, <strong>and</strong> gonads at different gonadal stages suggested the possible involvement of two<br />

Kiss genes in the brain <strong>and</strong> Kiss1 in the gonads of chub mackerel during seasonal gonadal<br />

development.<br />

2. Selvaraj S., H. Kitano, Y. Fujinaga, M. Amano, A. Takahashi, A. Shimizu, M. Yoneda, A.<br />

Yamaguchi, <strong>and</strong> M. Matsuyama. 2009. Immunological characterization <strong>and</strong> distribution of<br />

three GnRH forms in the brain <strong>and</strong> pituitary gl<strong>and</strong> of chub mackerel (Scomber japonicus).<br />

Zool. Sci. 26: 828-839.<br />

This study reports on the presence of three GnRH forms in the brain of the chub mackerel,<br />

Scomber japonicus, namely, salmon GnRH (sGnRH), chicken GnRH-II (cGnRH-II), <strong>and</strong><br />

seabream GnRH (sbGnRH), as confirmed by combined high performance liquid chromatography<br />

(HPLC) <strong>and</strong> time-resolved fluoroimmunoassay (TR-FIA). Immunocytochemical localization of<br />

the three GnRH forms in the brain was investigated by using specific antisera, to elucidate<br />

possible roles of each GnRH form in reproduction in this species, <strong>and</strong> double immunolabeling<br />

was used to localize GnRH-ir (immunoreactive) fibers innervating the pituitary. The results of the<br />

study indicated that multiple GnRH forms serve different functions, with sbGnRH having a<br />

significant role in reproduction in stimulating FSH- <strong>and</strong> LH-producing cells, <strong>and</strong> sGnRH <strong>and</strong><br />

cGnRH-II serving as neurotransmitters or neuromodulators.<br />

3. Shiraishi T., S.D. Ketkar, H. Kitano, M. Nyuji, A. Yamaguchi, <strong>and</strong> M. Matsuyama. 2008. Time<br />

course of final oocyte maturation <strong>and</strong> ovulation in chub mackerel Scomber japonicus induced<br />

by hCG <strong>and</strong> GnRHa. Fish. Sci. 74: 764-769.<br />

The question of whether the ovulation <strong>and</strong> spawning time in chub mackerel Scomber<br />

japonicus is entrained by a circadian rhythm was tested by administering human chorionic<br />

gonadotropin (hCG) <strong>and</strong> gonadotropin-releasing hormone analogue (GnRHa) at two ‘opposite’<br />

times, 14:00 <strong>and</strong> 02:00 hours, <strong>and</strong> the time courses of FOM <strong>and</strong> ovulation were compared. When<br />

hCG was injected, ovulation occurred 33 h post-injection in both groups. Similarly, ovulation<br />

began at 36 h post-injection of GnRHa, regardless of the timing of injection. These results<br />

indicated that timing of ovulation in chub mackerel depends on the timing of luteinizing hormone<br />

(LH) stimulation.<br />

4. The following are published reports of our reproductive studies in chub mackerel:<br />

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