畜牧兽医学报 ›› 2018, Vol. 49 ›› Issue (12): 2584-2592.doi: 10.11843/j.issn.0366-6964.2018.12.007

• 遗传育种 • 上一篇    下一篇

三种小分子化合物对猪胎儿成纤维细胞DNA精确修复效率的影响

李国玲1, 王豪强1, 阮晓芳1, 莫健新1, 全绒1, 钟翠丽1, 李紫聪1, 吴珍芳1,2, 刘德武1, 张献伟1,2*   

  1. 1. 华南农业大学 动物科学学院, 国家生猪种业工程技术研究中心, 广州 510642;
    2. 广东温氏食品集团股份有限公司, 新兴 527439
  • 收稿日期:2018-01-22 出版日期:2018-12-23 发布日期:2019-01-23
  • 通讯作者: 张献伟,博士,主要从事动物遗传育种研究,E-mail:zxianw@163.com
  • 作者简介:李国玲(1991-),男,广东云浮人,博士生,主要从事遗传育种与基因编辑研究,E-mail:792268184@qq.com
  • 基金资助:

    国家转基因重大专项(2016ZX08006002);粤西"扬帆计划"博士后人才扶持项目(2016)

Effect of Three Small Molecule Compounds on Precise DNA Repair Efficiency in Porcine Fetal Fibroblasts

LI Guo-ling1, WANG Hao-qiang1, RUAN Xiao-fang1, MO Jian-xin1, QUAN Rong1, ZHONG Cui-li1, LI Zi-cong1, WU Zhen-fang1,2, LIU De-wu1, ZHANG Xian-wei1,2*   

  1. 1. National Engineering Research Center for Breeding Swine Industry, College of Animal Science, South China Agricultural University, Guangzhou 510642, China;
    2. Guangdong Wens Foodstuff Group Co., Ltd, Xinxing 527439, China
  • Received:2018-01-22 Online:2018-12-23 Published:2019-01-23

摘要:

旨在研究3种小分子化合物(RS-1、Chir99021和PD173074)对猪胎儿成纤维细胞DNA精确修复效率的影响。本研究以猪胎儿成纤维细胞(porcine fetal fibroblasts,PFFs)为试验对象,利用HDR通路关键因子Rad51激活剂RS-1、Wnt信号通路关键因子糖原合成酶激酶-3(glycogen synthase kinase 3,GSK-3)抑制剂Chir99021和成纤维细胞生长因子受体(fibroblast growth factor receptor,FGFR1)抑制剂PD173074培养细胞,通过流式细胞术检测绿色荧光细胞数百分比来验证3种小分子化合物对DNA精确修复效率的影响。结果显示:1)经不同剂量的Chir99021和PD173074处理后,PFFs DNA损伤修复因子LIG4、NHEJ1、XRCC5、XRCC6和Rad51表达水平都显著下调(P<0.05),而经不同浓度PD173074(0.1~0.5 μmol·L-1)处理后,PNKP因子表达上调(P<0.05)。2)Chir99021低剂量时可显著提高同源重组修复(homologous recombination,HR)介导的同源重组效率,Chir99021高剂量时可显著提高单链退火修复(single strand annealing,SSA)介导的同源重组效率;RS-1和PD173074低剂量时可显著提高HR效率(P<0.05),但RS-1在高浓度时显著下调SSA修复效率(P<0.05),而PD173074对SSA效率无显著影响(P>0.05);此外单链寡核苷酸介导的DNA修复(single-stranded oligonucleotide,ssODN)效率并不受小分子化合物处理的影响(P>0.05)。本研究结果表明,适当浓度小分子化合物的应用有利于不同策略的基因敲入细胞系的产生,为获得精确的遗传修饰的动物模型打基础。

关键词: 同源重组修复, 非同源重组, Chir99021, RS-1, PD173074

Abstract:

The aim of this study was to investigate the effects of 3 small molecule compounds (RS-1, Chir99021 and PD173074) on the DNA precise repair efficiency in porcine fetal fibroblasts. In this study,the activator RS-1 for Rad51, the inhibitor Chir99021 for glycogen synthase kinase 3 (GSK-3) and the inhibitor PD173074 for fibroblast growth factor receptor (FGFR1) were used to culture porcine fetal fibroblasts, and then the percentage of green fluorescent cells was detected by flow cytometry to verify the effect of 3 small molecule compounds on DNA repair efficiency. The results showed that:1) After treatment with different doses of Chir99021 and PD173074, the expression levels of PFFs DNA damage repair factors LIG4, NHEJ1, XRCC5, XRCC6 and Rad51 were significantly down-regulated (P<0.05), and after treatment with different doses of of PD173074, the expression level of PNKP factor was significantly up-regulated (P<0.05).2) The low dose of Chir99021 significantly increased the efficiency of homologous recombination (P<0.05) mediated by homologous recombination (HR) repair(P<0.05). High dose of Chir99021 could significantly improve the efficiency of homologous recombination mediated by single strand annealing (SSA) repair(P<0.05).The low doses of RS-1 and PD173074 significantly increased HR efficiency (P<0.05), but RS-1 significantly down-regulated SSA repair efficiency at high concentration (P<0.05), while PD173074 had no significant effect on SSA efficiency (P>0.05). Furthermore, the single-stranded oligonucleotide-mediated DNA repair (ssODN) was not affected (P>0.05) by small molecule compounds. This study indicates that the application of small molecule compounds with appropriate concentrations will facilitate the generation of gene knock-in cell lines, which laying the foundation for obtaining genetic modification animal models.

Key words: homologous recombination repair, nonhomologous recombination, Chir99021, RS-1, PD173074

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