Generation and characterization of neurogenin1-GFP transgenic medaka with potential for rapid developmental neurotoxicity screening

被引:5
作者
Fan, Chun-Yang [1 ,2 ,3 ]
Simmons, Steven O. [1 ,2 ]
Law, Sheran H. W. [4 ]
Jensen, Karl [1 ,2 ]
Cowden, John [1 ,2 ]
Hinton, David [4 ]
Padilla, Stephanie [1 ,2 ]
Ramabhadran, Ram [1 ,2 ]
机构
[1] US EPA, Integrated Syst Toxicol Div, Natl Hlth & Environm Effects Res Lab, Res Triangle Pk, NC 27711 USA
[2] US EPA, Tox Assessment Div, Natl Hlth & Environm Effects Res Lab, Res Triangle Pk, NC 27711 USA
[3] Univ N Carolina, Curriculum Toxicol, Chapel Hill, NC 27599 USA
[4] Duke Univ, Nicholas Sch Environm & Earth Sci, Environm Sci & Policy Div, Durham, NC 27708 USA
关键词
Transgenic medaka; Zebrafish neurogenin 1; GFP; Developmental neurotoxicity screening; I-SCEI MEGANUCLEASE; HIGHLY EFFICIENT TRANSGENESIS; GERM-LINE TRANSMISSION; ORYZIAS-LATIPES; MEDIATED TRANSGENESIS; REGULATORY ELEMENTS; ZEBRAFISH EMBRYOS; FISH; GENES; EXPRESSION;
D O I
10.1016/j.aquatox.2011.05.017
中图分类号
Q17 [水生生物学];
学科分类号
071004 [水生生物学];
摘要
Fish models such as zebrafish and medaka are increasingly used as alternatives to rodents in developmental and toxicological studies. These developmental and toxicological studies can be facilitated by the use of transgenic reporters that permit the real-time, noninvasive observation of the fish. Here we report the construction and characterization of transgenic medaka lines expressing green fluorescent protein (GFP) under the control of the zebrafish neurogenin 1 (ngn1) gene promoter. Neurogenin (ngn1) is a helix-loop-helix transcription factor expressed in proliferating neuronal progenitor cells early in neuronal differentiation and plays a crucial role in directing neurogenesis. GFP expression was detected from 24 h post-fertilization until hatching, in a spatial pattern consistent with the previously reported zebrafish ngn1 expression. Temporal expression of the transgene parallels the expression profile of the endogenous medaka ngn1 transcript. Further, we demonstrate that embryos from the transgenic line permit the non-destructive, real-time screening of ngn1 promoter-directed GFP expression in a 96-well format, enabling higher throughput studies of developmental neurotoxicants. This strain has been deposited with and maintained by the National BioResource Project and is available on request (http://www.shigen.nig.ac.jp/medaka/strainDetailAction.do?quickSearch=true&strainld=5660). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 135
页数:9
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