{"title":"建立新型克隆 GFP 表达转基因银鲫。","authors":"Ren Uehara , Shinji Takeda , Daichi Oku , Ryo Sasaki , Masaru Murakami , Hajime Shiba , Fumihiko Katakura , Tadaaki Moritomo","doi":"10.1016/j.dci.2024.105290","DOIUrl":null,"url":null,"abstract":"<div><div>The clonal triploid ginbuna crucian carp <em>Carassius auratus langsdorfii</em>, a naturally occurring gynogenetic fish, is suitable for cell transplantation studies to reveal the roles of stem cells and immune cells. To ensure long-term traceability of donor cells within recipient fish, we have established a transgenic ginbuna line that expresses green fluorescent protein (GFP). The <em>Xenopus laevis ef1a</em> promoter was introduced for regulating GFP expression. <em>Tol2</em> transposon-based transgenesis to ginbuna embryos resulted in producing a putative founder fish (F0) in a mosaic fluorescent fashion; the frequency of germline transmission was 14.9%. All embryos of GFP-positive offspring (F1)-derived F2 generation expressed GFP widely across the body. The result of Southern blot analysis showed that the transgene was present on a single DNA fragment of equivalent size among F1 and F2 individuals tested, indicating that the transgene was stably transmitted without translocation. Analysis of the fluorescence intensity of organs obtained from F1 and F2 juveniles using fluorescence microscope showed that eyes, brain, skeletal muscle, heart and gonad exhibited a strong GFP fluorescence while gill, spleen and intestine gave a weak signal; no fluorescence was observed in erythrocytes. Flow cytometric analyses of peripheral leukocytes from F1 and F2 adult fish revealed all cell populations expressed GFP. Scale grafts from the transgenic fish to the wild-type fish exhibited persistent engraftment. Together, our transgenic line can be a powerful tool for studying cellular dynamics by cell transplantation and provide a solid basis for further immunological research advances in teleost.</div></div>","PeriodicalId":11228,"journal":{"name":"Developmental and comparative immunology","volume":"162 ","pages":"Article 105290"},"PeriodicalIF":2.7000,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Establishment of a novel clonal GFP-expressing transgenic ginbuna crucian carp\",\"authors\":\"Ren Uehara , Shinji Takeda , Daichi Oku , Ryo Sasaki , Masaru Murakami , Hajime Shiba , Fumihiko Katakura , Tadaaki Moritomo\",\"doi\":\"10.1016/j.dci.2024.105290\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The clonal triploid ginbuna crucian carp <em>Carassius auratus langsdorfii</em>, a naturally occurring gynogenetic fish, is suitable for cell transplantation studies to reveal the roles of stem cells and immune cells. To ensure long-term traceability of donor cells within recipient fish, we have established a transgenic ginbuna line that expresses green fluorescent protein (GFP). The <em>Xenopus laevis ef1a</em> promoter was introduced for regulating GFP expression. <em>Tol2</em> transposon-based transgenesis to ginbuna embryos resulted in producing a putative founder fish (F0) in a mosaic fluorescent fashion; the frequency of germline transmission was 14.9%. All embryos of GFP-positive offspring (F1)-derived F2 generation expressed GFP widely across the body. The result of Southern blot analysis showed that the transgene was present on a single DNA fragment of equivalent size among F1 and F2 individuals tested, indicating that the transgene was stably transmitted without translocation. Analysis of the fluorescence intensity of organs obtained from F1 and F2 juveniles using fluorescence microscope showed that eyes, brain, skeletal muscle, heart and gonad exhibited a strong GFP fluorescence while gill, spleen and intestine gave a weak signal; no fluorescence was observed in erythrocytes. Flow cytometric analyses of peripheral leukocytes from F1 and F2 adult fish revealed all cell populations expressed GFP. Scale grafts from the transgenic fish to the wild-type fish exhibited persistent engraftment. Together, our transgenic line can be a powerful tool for studying cellular dynamics by cell transplantation and provide a solid basis for further immunological research advances in teleost.</div></div>\",\"PeriodicalId\":11228,\"journal\":{\"name\":\"Developmental and comparative immunology\",\"volume\":\"162 \",\"pages\":\"Article 105290\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-11-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Developmental and comparative immunology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0145305X24001629\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"FISHERIES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental and comparative immunology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0145305X24001629","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0
摘要
克隆三倍体银鲫(Carassius auratus langsdorfii)是一种天然雌雄同体鱼类,适合用于细胞移植研究,以揭示干细胞和免疫细胞的作用。为了确保受体鱼体内供体细胞的长期可追溯性,我们建立了一个表达绿色荧光蛋白(GFP)的转基因金线鱼品系。为了调节 GFP 的表达,我们引入了 Xenopus laevis ef1a 启动子。基于 Tol2 转座子的转基因技术可在金枪鱼胚胎中以镶嵌荧光方式产生推定的创始鱼(F0),种系传递频率为 14.9%。GFP 阳性后代(F1)产生的 F2 代的所有胚胎都在全身广泛表达 GFP。Southern 印迹分析的结果表明,受测的 F1 和 F2 个体中,转基因存在于大小相当的单个 DNA 片段上,表明转基因是稳定传递的,没有发生易位。利用荧光显微镜对 F1 和 F2 幼体器官的荧光强度进行分析表明,眼睛、大脑、骨骼肌、心脏和性腺显示出较强的 GFP 荧光,而鳃、脾脏和肠道则显示出微弱的信号;红细胞未观察到荧光。对 F1 和 F2 成鱼外周白细胞的流式细胞分析显示,所有细胞群都表达了 GFP。从转基因鱼到野生型鱼的鳞片移植显示出持续的接种。总之,我们的转基因品系可以成为通过细胞移植研究细胞动态的有力工具,并为进一步推进远洋鱼类的免疫学研究奠定坚实的基础。
Establishment of a novel clonal GFP-expressing transgenic ginbuna crucian carp
The clonal triploid ginbuna crucian carp Carassius auratus langsdorfii, a naturally occurring gynogenetic fish, is suitable for cell transplantation studies to reveal the roles of stem cells and immune cells. To ensure long-term traceability of donor cells within recipient fish, we have established a transgenic ginbuna line that expresses green fluorescent protein (GFP). The Xenopus laevis ef1a promoter was introduced for regulating GFP expression. Tol2 transposon-based transgenesis to ginbuna embryos resulted in producing a putative founder fish (F0) in a mosaic fluorescent fashion; the frequency of germline transmission was 14.9%. All embryos of GFP-positive offspring (F1)-derived F2 generation expressed GFP widely across the body. The result of Southern blot analysis showed that the transgene was present on a single DNA fragment of equivalent size among F1 and F2 individuals tested, indicating that the transgene was stably transmitted without translocation. Analysis of the fluorescence intensity of organs obtained from F1 and F2 juveniles using fluorescence microscope showed that eyes, brain, skeletal muscle, heart and gonad exhibited a strong GFP fluorescence while gill, spleen and intestine gave a weak signal; no fluorescence was observed in erythrocytes. Flow cytometric analyses of peripheral leukocytes from F1 and F2 adult fish revealed all cell populations expressed GFP. Scale grafts from the transgenic fish to the wild-type fish exhibited persistent engraftment. Together, our transgenic line can be a powerful tool for studying cellular dynamics by cell transplantation and provide a solid basis for further immunological research advances in teleost.
期刊介绍:
Developmental and Comparative Immunology (DCI) is an international journal that publishes articles describing original research in all areas of immunology, including comparative aspects of immunity and the evolution and development of the immune system. Manuscripts describing studies of immune systems in both vertebrates and invertebrates are welcome. All levels of immunological investigations are appropriate: organismal, cellular, biochemical and molecular genetics, extending to such fields as aging of the immune system, interaction between the immune and neuroendocrine system and intestinal immunity.