Funabara Daisuke, Ohmori Fumito, Kinoshita Shigeharu, Koyama Hiroki, Mizutani Saeri, Ota Ayaka, Osakabe Yuki, Nagai Kiyohito, Maeyama Kaoru, Okamoto Kikuhiko, Kanoh Satoshi, Asakawa Shuichi, Watabe Shugo
Graduate School of Bioresources, Mie University, Tsu, Mie, Japan.
Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan.
PLoS One. 2014 Jan 15;9(1):e84706. doi: 10.1371/journal.pone.0084706. eCollection 2014.
In our previous publication, we identified novel gene candidates involved in shell formation by EST analyses of the nacreous and prismatic layer-forming tissues in the pearl oyster Pinctada fucata. In the present study, 14 of those genes, including two known genes, were selected and further examined for their involvement in shell formation using the RNA interference. Molecular characterization based on the deduced amino acid sequences showed that seven of the novel genes encode secretory proteins. The tissue distribution of the transcripts of the genes, as analyzed by RT-PCR and in situ hybridization, was mostly consistent with those obtained by the EST analysis reported previously. Shells in the pearl oysters injected with dsRNAs targeting genes 000027, 000058, 000081, 000096, 000113 (nacrein), 000118, 000133 and 000411 (MSI60), which showed expression specific to the nacreous layer forming tissues, showed abnormal surface appearance in this layer. Individuals injected with dsRNAs targeting genes 000027, 000113 and 000133 also exhibited abnormal prismatic layers. Individuals injected with dsRNAs targeting genes 000031, 000066, 000098, 000145, 000194 and 000200, which showed expression specific to prismatic layer forming tissues, displayed an abnormal surface appearance in both the nacreous and prismatic layers. Taken together, the results suggest that the genes involved in prismatic layer formation might also be involved in the formation of the nacreous layers.
在我们之前的出版物中,通过对合浦珠母贝珍珠层和棱柱层形成组织的EST分析,我们鉴定出了参与贝壳形成的新基因候选物。在本研究中,从这些基因中选择了14个,包括两个已知基因,并使用RNA干扰进一步检测它们在贝壳形成中的作用。基于推导的氨基酸序列的分子特征表明,其中7个新基因编码分泌蛋白。通过RT-PCR和原位杂交分析的这些基因转录本的组织分布,大多与之前报道的EST分析结果一致。向合浦珠母贝注射靶向基因000027、000058、000081、000096、000113(珍珠质蛋白)、000118、000133和000411(MSI60)的dsRNA,这些基因在珍珠层形成组织中表现出特异性表达,注射后的贝壳在该层出现异常表面外观。注射靶向基因000027、000113和000133的dsRNA个体的棱柱层也表现异常。向合浦珠母贝注射靶向基因000031、000066、000098、000145、000194和000200的dsRNA,这些基因在棱柱层形成组织中表现出特异性表达,注射后的个体在珍珠层和棱柱层均出现异常表面外观。综上所述,结果表明参与棱柱层形成的基因可能也参与珍珠层的形成。