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| 抑制Ligase4或Xrcc6活性增强斑马鱼原始生殖细胞中DNA同源重组的效率 | |
| 引用本文： | 魏志强,熊凤,何牡丹,王厚鹏,朱作言,孙永华. 抑制Ligase4或Xrcc6活性增强斑马鱼原始生殖细胞中DNA同源重组的效率[J]. 水生生物学报, 2015, 39(2): 339-348. DOI: 10.7541/2015.45 |
| 作者姓名： | 魏志强 熊凤 何牡丹 王厚鹏 朱作言 孙永华 |
| 作者单位： | 1. 中国科学院水生生物研究所淡水生态与生物技术国家重点实验室, 武汉 430072; 2. 中国科学院大学, 北京 100049; 3. 湖北医药学院附属太和医院生物医学研究所, 十堰, 442000 |
| 基金项目： | The National Basic Research Program of China (grant numbers 2010CB126306 & 2012CB944504); the National Science Fund for Excellent Young Scholars of NSFC (grant number 31222052); the FEBL grant 2011FBZ23 |
| 摘 要： | 利用斑马鱼作为体内模型, 研究旨在提高斑马鱼原始生殖细胞(Primordial germ cells, PGCs)中同源重组(Homologous recombination, HR)的效率。首先, 将UAS:mRFP-nos1载体显微注射到Tg (kop:KalTA4) 转基因胚胎中标记转基因PGCs, 结果表明筛选PGCs特异表达mRFP的胚胎能够相对提高转基因的生殖系传递效率。随后建立了PGCs中HR效率的评估体系, 并且证明抑制DNA ligase IV(Lig4)和Xrcc6(曾用名Ku70)的活性不但在全胚胎水平, 而且在PGCs水平都能够显著提高HR的效率。研究表明Tg (kop:KalTA4) 转基因品系是开展HR介导的基因打靶的一个有效平台。 |
| 关 键 词： | 斑马鱼 原始生殖细胞 基因打靶 同源重组 Ligase 4 Xrcc6 |
| 收稿时间： | 2014-04-21 |
SUPPRESSION OF LIGASE4 OR XRCC6 ACTIVITIES ENHANCES THE DNA HOMOLOGOUS RECOMBINATION EFFICIENCY IN ZEBRAFISH PRIMORDIAL GERM CELLS |
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| Wei Zhi-Qiang,Xiong Feng,He Mu-Dan,Wang Hou-Peng,Zhu Zuo-Yan,Sun Yong-Hua. SUPPRESSION OF LIGASE4 OR XRCC6 ACTIVITIES ENHANCES THE DNA HOMOLOGOUS RECOMBINATION EFFICIENCY IN ZEBRAFISH PRIMORDIAL GERM CELLS[J]. Acta Hydrobiologica Sinica, 2015, 39(2): 339-348. DOI: 10.7541/2015.45 | |
| Authors: | Wei Zhi-Qiang Xiong Feng He Mu-Dan Wang Hou-Peng Zhu Zuo-Yan Sun Yong-Hua |
| Affiliation: | 1. State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China; 2. University of Chinese Academy of Sciences, Beijing 100049, China; 3. Institute of Biomedicine, Taihe Hospital, Hubei University of Medicine, Shiyan 442000, China |
| Abstract: | Primordial germ cells (PGCs) give rise to gametes which transmit the genetic information to next generation, therefore PGCs provide us an ideal cell type for genetic manipulation. Homologous recombination (HR) is the most efficient technique to create designed genetic modifications, however, its efficiency is rather low in vertebrates. In this study, by using zebrafish as an in vivo model, we aimed to enhance the efficiency of HR in zebrafish PGCs. First, we injected UAS:mRFP-nos1 construct into Tg (kop:KalTA4) embryos to label the transgenic PGCs, and we showed that screening of PGCs-specific mRFP expression led to relatively high-efficient germline transmission of transgene. Then we established an in vivo assay to evaluate the HR frequency in PGCs. We further revealed that suppression of the activities of DNA ligase IV (Lig4) and Xrcc6 (previously known as Ku70) could significantly increase the HR efficiency, not only at whole embryo level but also in PGCs. We proposed that the Tg(kop:KalTA4) line could be used as an effective platform for HR-mediated gene targeting. |
| Keywords: | Zebrafish Primordial germ cells Gene targeting Homologous recombination Ligase 4 Xrcc6 |
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