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      Development of genome engineering technologies in cattle: from random to specific

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          Abstract

          The production of transgenic farm animals (e.g., cattle) via genome engineering for the gain or loss of gene functions is an important undertaking. In the initial stages of genome engineering, DNA micro-injection into one-cell stage embryos (zygotes) followed by embryo transfer into a recipient was performed because of the ease of the procedure. However, as this approach resulted in severe mosaicism and has a low efficiency, it is not typically employed in the cattle as priority, unlike in mice. To overcome the above issue with micro-injection in cattle, somatic cell nuclear transfer (SCNT) was introduced and successfully used to produce cloned livestock. The application of SCNT for the production of transgenic livestock represents a significant advancement, but its development speed is relatively slow because of abnormal reprogramming and low gene targeting efficiency. Recent genome editing technologies (e.g., ZFN, TALEN, and CRISPR-Cas9) have been rapidly adapted for applications in cattle and great results have been achieved in several fields such as disease models and bioreactors. In the future, genome engineering technologies will accelerate our understanding of genetic traits in bovine and will be readily adapted for bio-medical applications in cattle.

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          Most cited references38

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          Altering the genome by homologous recombination.

          M Capecchi (1989)
          Homologous recombination between DNA sequences residing in the chromosome and newly introduced, cloned DNA sequences (gene targeting) allows the transfer of any modification of the cloned gene into the genome of a living cell. This article discusses the current status of gene targeting with particular emphasis on germ line modification of the mouse genome, and describes the different methods so far employed to identify those rare embryonic stem cells in which the desired targeting event has occurred.
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            Gene targeting in mice: functional analysis of the mammalian genome for the twenty-first century.

            Gene targeting in mouse embryonic stem cells has become the 'gold standard' for determining gene function in mammals. Since its inception, this technology has revolutionized the study of mammalian biology and human medicine. Here I provide a personal account of the work that led to the generation of gene targeting which now lies at the centre of functional genomic analysis.
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              Gene-edited CRISPR mushroom escapes US regulation.

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                Author and article information

                Contributors
                +82-2-880-1280 , snujang@snu.ac.kr
                Journal
                J Anim Sci Biotechnol
                J Anim Sci Biotechnol
                Journal of Animal Science and Biotechnology
                BioMed Central (London )
                1674-9782
                2049-1891
                30 January 2018
                30 January 2018
                2018
                : 9
                : 16
                Affiliations
                [1 ]ISNI 0000 0004 0470 5905, GRID grid.31501.36, Department of Veterinary Clinical Science, College of Veterinary Medicine and the Research Institute of Veterinary Science, , Seoul National University, ; Seoul, 08826 Republic of Korea
                [2 ]ISNI 0000 0004 0470 5905, GRID grid.31501.36, Farm Animal Clinical Training and Research Center, Institute of GreenBio Science Technology, Seoul National University, ; PyeongChang-Gun, Gangwon-do 25354 Republic of Korea
                [3 ]GRID grid.410897.3, Emergence Center for Food-Medicine Personalized Therapy System, Advanced Institutes of Convergence Technology, Seoul National University, ; SuWon, Gyeonggi-do 16629 Republic of Korea
                [4 ]ISNI 0000 0004 0470 5905, GRID grid.31501.36, College of Veterinary Medicine, Seoul National University, ; #85, Room631, 1 Gwanak-ro, Gwanak-gu, Seoul, 08826 Republic of Korea
                Author information
                http://orcid.org/0000-0003-3804-1871
                Article
                232
                10.1186/s40104-018-0232-6
                5789629
                29423215
                9477f57a-c968-4467-bcd8-19a0948903ac
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
                : 10 July 2017
                : 9 January 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003725, National Research Foundation of Korea;
                Award ID: 2017R1A2B3004972
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100003668, Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry and Fisheries;
                Award ID: No. 109023-05-5-CG000
                Award Recipient :
                Funded by: BK21
                Award ID: BK21
                Award Recipient :
                Categories
                Review
                Custom metadata
                © The Author(s) 2018

                Animal science & Zoology
                cattle,crispr-cas9,genome engineering technologies,transgenesis,transposon

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