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      One-step generation of multiple transgenic mouse lines using an improved Pronuclear Injection-based Targeted Transgenesis ( i-PITT)

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          Abstract

          Background

          The pronuclear injection (PI) is the simplest and widely used method to generate transgenic (Tg) mice. Unfortunately, PI-based Tg mice show uncertain transgene expression due to random transgene insertion in the genome, usually with multiple copies. Thus, typically at least three or more Tg lines are produced by injecting over 200 zygotes and the best line/s among them are selected through laborious screening steps. Recently, we developed technologies using Cre- loxP system that allow targeted insertion of single-copy transgene into a predetermined locus through PI. We termed the method as PI-based Targeted Transgenesis (PITT). A similar method using PhiC31- attP/ B system was reported subsequently.

          Results

          Here, we developed an improved-PITT ( i-PITT) method by combining Cre- loxP, PhiC31- attP/ B and FLP- FRT systems directly under C57BL/6N inbred strain, unlike the mixed strain used in previous reports. The targeted Tg efficiency in the i-PITT typically ranged from 10 to 30%, with 47 and 62% in two of the sessions, which is by-far the best Tg rate reported. Furthermore, the system could generate multiple Tg mice simultaneously. We demonstrate that injection of up to three different Tg cassettes in a single injection session into as less as 181 zygotes resulted in production of all three separate Tg DNA containing targeted Tg mice.

          Conclusions

          The i-PITT system offers several advantages compared to previous methods: multiplexing capability ( i-PITT is the only targeted-transgenic method that is proven to generate multiple different transgenic lines simultaneously), very high efficiency of targeted-transgenesis (up to 62%), significantly reduces animal numbers in mouse-transgenesis and the system is developed under C57BL/6N strain, the most commonly used pure genetic background. Further, the i-PITT system is freely accessible to scientific community.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12864-015-1432-5) contains supplementary material, which is available to authorized users.

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          Most cited references28

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          Partitioning of lipid-modified monomeric GFPs into membrane microdomains of live cells.

          Many proteins associated with the plasma membrane are known to partition into submicroscopic sphingolipid- and cholesterol-rich domains called lipid rafts, but the determinants dictating this segregation of proteins in the membrane are poorly understood. We suppressed the tendency of Aequorea fluorescent proteins to dimerize and targeted these variants to the plasma membrane using several different types of lipid anchors. Fluorescence resonance energy transfer measurements in living cells revealed that acyl but not prenyl modifications promote clustering in lipid rafts. Thus the nature of the lipid anchor on a protein is sufficient to determine submicroscopic localization within the plasma membrane.
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            Bright and stable near infra-red fluorescent protein for in vivo imaging

            The ability of non-invasive monitoring of deep-tissue developmental, metabolic, and pathogenic processes will advance modern biotechnology. Imaging of live mammals using fluorescent probes is more feasible within a “near-infrared optical window” (NIRW) 1 . Here we report a phytochrome-based near infra-red fluorescent protein (iRFP) with the excitation/emission maxima at 690/713 nm. Bright fluorescence in a living mouse proved iRFP to be a superior probe for non-invasive imaging of internal mammalian tissues. Its high intracellular stability, low cytotoxicity, and lack of the requirement to add external biliverdin-chromophore makes iRFP as easy to use as conventional GFP-like proteins. Compared to earlier phytochrome-derived fluorescent probes, the iRFP protein has better in vitro characteristics and performs well in cells and in vivo, having greater effective brightness and photostability. Compared to the far-red GFP-like proteins, iRFP has substantially higher signal to background ratio in a mouse model owing to its infra-red shifted spectra.
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              Codon-improved Cre recombinase (iCre) expression in the mouse.

              By applying the mammalian codon usage to Cre recombinase, we improved Cre expression, as determined by immunoblot and functional analysis, in three different mammalian cell lines. The improved Cre (iCre) gene was also designed to reduce the high CpG content of the prokaryotic coding sequence, thereby reducing the chances of epigenetic silencing in mammals. Transgenic iCre expressing mice were obtained with good frequency, and in these mice loxP-mediated DNA recombination was observed in all cells expressing iCre. Moreover, iCre fused to two estrogen receptor hormone binding domains for temporal control of Cre activity could also be expressed in transgenic mice. However, Cre induction after administration of tamoxifen yielded only low Cre activity. Thus, whereas efficient activation of Cre fusion proteins in the brain needs further improvements, our studies indicate that iCre should facilitate genetic experiments in the mouse. Copyright 2002 Wiley-Liss, Inc.
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                Author and article information

                Contributors
                masato@is.icc.u-tokai.ac.jp
                hiromi@tokai-u.jp
                jmochida@rtc.riken.jp
                m-hirose@rtc.riken.jp
                a-hasegawa@rtc.riken.jp
                ogura@rtc.riken.jp
                ryuta@tokai-u.jp
                kimura@is.icc.u-tokai.ac.jp
                isotani@biken.osaka-u.ac.jp
                ikawa@biken.osaka-u.ac.jp
                masasato@ms.kagoshima-u.ac.jp
                cgurumurthy@unmc.edu
                Journal
                BMC Genomics
                BMC Genomics
                BMC Genomics
                BioMed Central (London )
                1471-2164
                9 April 2015
                9 April 2015
                2015
                : 16
                : 1
                : 274
                Affiliations
                [ ]Department of Molecular Life Science, Division of Basic Medical Science and Molecular Medicine, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 259-1193 Japan
                [ ]RIKEN BioResource Center, 3-1-1 Koyadai, Tsukuba, Ibaraki 305-0074 Japan
                [ ]Graduate School of Life and Environmental Science, University of Tsukuba, 1-1-1 Ten-noudai, Tsukuba, Ibaraki 305-8572 Japan
                [ ]Graduate School of Engineering, Tokai University, Kitakaname, Hiratsuka, Kanagawa 259-1292 Japan
                [ ]Immunology Frontier Research Center, Osaka University, 3-1 Yamadaoka, Suita, Osaka 565-0871 Japan
                [ ]Research Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Osaka 565-0871 Japan
                [ ]Section of Gene Expression Regulation, Frontier Science Research Center, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima, Kagoshima 890-8544 Japan
                [ ]Mouse Genome Engineering Core Facility, Department of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE 68198 USA
                Article
                1432
                10.1186/s12864-015-1432-5
                4404087
                25887549
                07542768-0903-46df-b675-7682ac62b5dc
                © Ohtsuka et al.; licensee BioMed Central. 2015

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 18 February 2015
                : 4 March 2015
                Categories
                Methodology Article
                Custom metadata
                © The Author(s) 2015

                Genetics
                transgenic mouse,pronuclear injection-based targeted transgenesis,cre-loxp,phic31-attp/b,flp-frt,rosa26,transportation of the cauda epididymides

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