Zheng Zhe, Du Xiaodong, Xiong Xinwei, Jiao Yu, Deng Yuewen, Wang Qingheng, Huang Ronglian
Fishery College, Guangdong Ocean University, Zhanjiang, China.
Guangdong Technology Research Center for Pearl Aquaculture and Process, Guangdong Ocean University, Zhanjiang, China.
PLoS One. 2017 Jun 1;12(6):e0178561. doi: 10.1371/journal.pone.0178561. eCollection 2017.
Heterodimeric PEBP2/CBFs are key regulators in diverse biological processes, such as haematopoietic stem-cell generation, bone formation and cancers. In this work, we cloned runt-like transcriptional factor (designated as PmRunt) and CBF β (designated as PmCBF) gene, which comprise the heterodimeric transcriptional factor in Pinctada martensii. PmRunt was identified with an open reading frame that encodes 545 amino acids and has typical Runt domain. Phylogenetic analysis results speculated that runt-like transcriptional factors (RDs) in vertebrates and invertebrates are separated into two branches. In molluscs, PmRunt and other RDs are clustered in one of these branches. Direct interaction between PmRunt and PmCBF was evidenced by yeast two-hybrid assay results. Gene repression by RNA interference decreased the expression level of PmRunt, and subsequent observation of the inner surface of the nacre by scanning electron microscopy demonstrated disordered growth. The luciferase activities of reporters that contain promoter regions of Collagen VI-like (PmColVI) and PmNacrein were enhanced by PmRunt. Meanwhile, Pm-miR-183 apparently inhibited the relative luciferase activity of reporters containing the 3'-UTR of PmRunt. The expression level of PmRunt was repressed after Pm-miR-183 was overexpressed in the mantle tissue. Therefore, we proposed that PmRunt could be targeted by Pm-miR-183 and regulate the transcription of PmColVI and PmNacrein by increasing their transcriptional activity, thereby governing nacre formation.
异源二聚体PEBP2/CBFs是多种生物过程中的关键调节因子,如造血干细胞生成、骨形成和癌症。在本研究中,我们克隆了合浦珠母贝中构成异源二聚体转录因子的类Runt转录因子(命名为PmRunt)和CBFβ(命名为PmCBF)基因。PmRunt被鉴定出具有一个编码545个氨基酸的开放阅读框,并具有典型的Runt结构域。系统发育分析结果推测,脊椎动物和无脊椎动物中的类Runt转录因子(RDs)分为两个分支。在软体动物中,PmRunt和其他RDs聚集在其中一个分支中。酵母双杂交试验结果证明了PmRunt和PmCBF之间的直接相互作用。RNA干扰导致的基因抑制降低了PmRunt的表达水平,随后通过扫描电子显微镜观察珍珠层内表面显示生长紊乱。PmRunt增强了含有类胶原蛋白VI(PmColVI)和PmNacrein启动子区域的报告基因的荧光素酶活性。同时,Pm-miR-183明显抑制了含有PmRunt 3'-UTR的报告基因的相对荧光素酶活性。在套膜组织中过表达Pm-miR-183后,PmRunt的表达水平受到抑制。因此,我们提出PmRunt可能是Pm-miR-183的靶标,并通过增加其转录活性来调节PmColVI和PmNacrein的转录,从而控制珍珠层的形成。