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Molecular cloning, expression pattern analysis, and in situ hybridization of a Transformer-2 gene in the oriental freshwater prawn, Macrobrachium nipponense (de Haan, 1849)

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Abstract

In this study, we isolated a full-length cDNA sequence from Macrobrachium nipponense and investigated its gene function. We named the gene Mntra-2a because of high similarities and close evolutionary divergence with arthropod tra-2. The full-length cDNA of Mntra-2a was 1293 bp, consisting of a 212 bp 5′ UTR, a 268 bp 3′ UTR, and an ORF of 813 bp encoding 270 amino acids. It contained an RNA recognition motif and a linker region. Real-time PCR analysis showed that Mntra-2a was highly expressed in the gonads of both males and females. Further in situ hybridization analysis showed that Mntra-2a was mainly located in oocytes and spermatocytes. During embryogenesis, Mntra-2a expression was higher in the cleavage and nauplius stages. During the ovarian reproductive cycle, Mntra-2a expression reached a peak at OvaryV and decreased to the lowest level at OvaryIV. These results indicated that Mntra-2a probably played important roles in embryonic development and early gonad development in M. nipponense. Our results provide basic information for further functional studies of tra-2 in M. nipponense.

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Acknowledgements

This research was supported by grants from the Jiangsu Agricultural Industry Technology System (JFRS-02); the National Key R&D Progrom of China (2018YFD0901303); National Natural Science Foundation of China (31572617); New varieties creation Major Project in Jiangsu province (PZCZ201745); China Agriculture Research System-48 (CARS-48); Central Public-interest Scientific Institution Basal Research Fund CAFS (2017JBFZ05); and Science and Technology Development Fund of Wuxi (CLE02N1514).

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Correspondence to Hongtuo Fu.

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Wang, Y., Jin, S., Fu, H. et al. Molecular cloning, expression pattern analysis, and in situ hybridization of a Transformer-2 gene in the oriental freshwater prawn, Macrobrachium nipponense (de Haan, 1849). 3 Biotech 9, 205 (2019). https://doi.org/10.1007/s13205-019-1737-1

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