Molecular cloning and expression pattern of oriental river prawn (Macrobrachium nipponense) nitric oxide synthase

作者：Rahman, N. M. A.; Fu, H. T.^*; Sun, S. M.; Qiao, H.; Jin, S.; Bai, H. K.; Zhang, W. Y.; Liang, G. X.; Gong, Y. S.; Xiong, Y. W.; Wu, Y.

来源：Genetics and Molecular Research, 2016, 15(3): 15038541.

DOI：10.4238/gmr.15038541

• Macrobrachium nipponense
• Nitric oxide synthase
• Cloning
• Expression pattern
• RT-qPCR
• Post-larvae

Nitric oxide synthase (NOS) produces nitric oxide (NO) by catalyzing the conversion of L-arginine to L-citrulline, with the concomitant oxidation of nicotinamide adenine dinucleotide phosphate. Recently, various studies have verified the importance of NOS invertebrates and invertebrates. However, the NOS gene family in the oriental river prawn Macrobrachium nipponense is poorly understood. In this study, we cloned the full-length NOS complementary DNA from M. nipponense (MnNOS) and characterized its expression pattern in different tissues and at different developmental stages. Real-time quantitative polymerase chain reaction (RT-qPCR) showed the MnNOS gene to be expressed in all investigated tissues, with the highest levels observed in the androgenic gland (P < 0.05). Our results revealed that the MnNOS gene may play a key role in M. nipponense male sexual differentiation. Moreover, RT-qPCR revealed that MnNOS mRNA expression was significantly increased in post-larvae 10 days after metamorphosis (P < 0.05). The expression of this gene in various tissues indicates that it may perform versatile biological functions in M. nipponense.

• 出版日期2016
• 单位中国水产科学研究院; 中国水产科学研究院淡水渔业研究中心; 南京农业大学