Production of Mutated Porcine Embryos Using Zinc Finger Nucleases and a Reporter-based Cell Enrichment System

To facilitate the construction of genetically-modified pigs, we produced cloned embryos derived from porcine fibroblasts transfected with a pair of engineered zinc finger nuclease (ZFN) plasmids to create targeted mutations and enriched using a reporter plasmid system. The reporter expresses RFP and...

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Bibliographic Details
Published in:Asian-australasian journal of animal sciences Vol. 27; no. 3; pp. 324 - 329
Main Authors: Koo, Ok Jae, Park, Sol Ji, Lee, Choongil, Kang, Jung Taek, Kim, Sujin, Moon, Joon Ho, Choi, Ji Yei, Kim, Hyojin, Jang, Goo, Kim, Jin-Soo, Kim, Seokjoong, Lee, Byeong-Chun
Format: Journal Article
Language:Korean
Published: 2014
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Summary:To facilitate the construction of genetically-modified pigs, we produced cloned embryos derived from porcine fibroblasts transfected with a pair of engineered zinc finger nuclease (ZFN) plasmids to create targeted mutations and enriched using a reporter plasmid system. The reporter expresses RFP and eGFP simultaneously when ZFN-mediated site-specific mutations occur. Thus, double positive cells ($RFP^+/eGFP^+$) were selected and used for somatic cell nuclear transfer. Two types of reporter based enrichment systems were used in this study; the cloned embryos derived from cells enriched using a magnetic sorting-based system showed better developmental competence than did those derived from cells enriched by flow cytometry. Mutated sequences, such as insertions, deletions, or substitutions, together with the wild-type sequence, were found in the cloned porcine blastocysts. Therefore, genetic mutations can be achieved in cloned porcine embryos reconstructed with ZFN-treated cells that were enriched by a reporter-based system.
Bibliography:KISTI1.1003/JNL.JAKO201409150680221
ISSN:1011-2367
1976-5517