Hu Guang-Wei, Yan Xi-Wu, Qin Yan-Jie, Nie Hong-Tao
Engineering and Technology Research Center of Shellfish Breeding in Liaoning Province, Dalian Ocean University, Dalian, 116023, China.
Mol Biol Rep. 2014 Jun;41(6):3583-90. doi: 10.1007/s11033-014-3221-7. Epub 2014 Feb 25.
Inhibitor of growth protein 3 (ING3), a new member of ING family, is involved in the regulation of various processes. In this study, a full-length cDNA of ING3 (named as RpING3) was cloned from the gill of Ruditapes philippinarum by rapid amplification of cDNA ends method for the first time. The cDNA obtained was 1442 bp exclusive of poly (A) residues with a 1248 bp open reading frame encoding 415 amino acids. The RpING3 protein has a calculated molecular weight of 46.59 kDa and isoelectric point of 6.62. Two conserved motif and some functional sites were found. Tissue distribution analysis of the RpING3 mRNA revealed that the RpING3 expression level was much higher in gill and digestive gland while lower in mantle, foot and adductor muscle. The temporal expression of RpING3 in digestive gland after lead exposure was recorded by quantitative real-time PCR. The result showed that RpING3 was rapidly up-regulated at 6 h post-exposure and reached tenfold of the control group. These results suggest that RpING3 dependent signaling pathway is present in Manila clam and RpING3 may play important roles in protecting cells from heavy metal damage in R. philippinarum.
生长抑制蛋白3(ING3)是ING家族的新成员,参与多种生理过程的调控。本研究首次采用cDNA末端快速扩增法从菲律宾蛤仔鳃中克隆出ING3的全长cDNA(命名为RpING3)。获得的cDNA长度为1442 bp(不包括poly(A)尾),开放阅读框为1248 bp,编码415个氨基酸。RpING3蛋白的计算分子量为46.59 kDa,等电点为6.62。发现了两个保守基序和一些功能位点。对RpING3 mRNA的组织分布分析表明,RpING3在鳃和消化腺中的表达水平较高,而在外套膜、足和闭壳肌中的表达水平较低。通过实时定量PCR记录了铅暴露后消化腺中RpING3的时序表达。结果显示,暴露后6小时RpING3迅速上调,达到对照组的10倍。这些结果表明,菲律宾蛤仔中存在依赖RpING3的信号通路,且RpING3可能在保护菲律宾蛤仔细胞免受重金属损伤方面发挥重要作用。