Zhao Chao, Dai Wenting, Qiu Lihua
South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou, China.
Key Laboratory of South China Sea Fishery Resources Exploitation & Utilization, Ministry of Agriculture, Guangzhou, China.
Genet Mol Biol. 2017 Jan-Mar;40(1):93-103. doi: 10.1590/1678-4685-GMB-2016-0144. Epub 2017 Mar 2.
P53 And DNA Damage-Regulated Gene 1 (PDRG1) is a novel gene which plays an important role in chaperone-mediated protein folding. In the present study, the full-length complementary DNA (cDNA) sequence of the PDRG1 gene from Penaeus monodon (PmPDRG1) was cloned by the rapid amplification of cDNA ends (RACE) method. The cDNA of PmPDRG1 spans 1,613 bp, interrupted by only one short intron, and encodes a protein of 136 amino acids with calculated molecular weight of 15.49 kDa. The temporal expression profile of PmPDRG1 in different tissues and in different developmental stages of the ovary was investigated by real-time quantitative PCR (RT-qPCR). An RNA interference (RNAi) experiment was performed to study the relationship between P. monodon p53 (Pmp53) and PmPDRG1, and the results showed that the relative expression level of PmPDRG1 mRNA was notably up-regulated from 12 h to 96 h after Pmp53 was silenced both in ovary and hepatopancreas. To further explore the role of PmPDRG1 in ovarian development, dopamine (DA) and 5-hydroxytryptamine (5-HT)-injected shrimps were analyzed by RT-qPCR, indicating that PmPDRG1 may be involved in the regulation of ovarian development of P. monodon.
P53与DNA损伤调节基因1(PDRG1)是一个新基因,在伴侣介导的蛋白质折叠中起重要作用。在本研究中,采用cDNA末端快速扩增(RACE)方法克隆了斑节对虾PDRG1基因(PmPDRG1)的全长互补DNA(cDNA)序列。PmPDRG1的cDNA全长1613 bp,仅被一个短内含子打断,编码一个由136个氨基酸组成的蛋白质,计算分子量为15.49 kDa。通过实时定量PCR(RT-qPCR)研究了PmPDRG1在不同组织和卵巢不同发育阶段的时空表达谱。进行了RNA干扰(RNAi)实验以研究斑节对虾p53(Pmp53)与PmPDRG1之间的关系,结果表明,在卵巢和肝胰腺中沉默Pmp53后12小时至96小时,PmPDRG1 mRNA的相对表达水平显著上调。为进一步探究PmPDRG1在卵巢发育中的作用,通过RT-qPCR分析了注射多巴胺(DA)和5-羟色胺(5-HT)的对虾,表明PmPDRG1可能参与斑节对虾卵巢发育的调控。