TY - JOUR
T1 - Direct introduction of gene constructs into the pronucleus-like structure of cloned embryos
T2 - a new strategy for the generation of genetically modified pigs
AU - Kurome, Mayuko
AU - Leuchs, Simon
AU - Kessler, Barbara
AU - Kemter, Elisabeth
AU - Jemiller, Eva Maria
AU - Foerster, Beatrix
AU - Klymiuk, Nikolai
AU - Zakhartchenko, Valeri
AU - Wolf, Eckhard
N1 - Publisher Copyright:
© 2016, Springer International Publishing Switzerland.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - Due to a rising demand of porcine models with complex genetic modifications for biomedical research, the approaches for their generation need to be adapted. In this study we describe the direct introduction of a gene construct into the pronucleus (PN)-like structure of cloned embryos as a novel strategy for the generation of genetically modified pigs, termed “nuclear injection”. To evaluate the reliability of this new strategy, the developmental ability of embryos in vitro and in vivo as well as the integration and expression efficiency of a transgene carrying green fluorescence protein (GFP) were examined. Eighty percent of the cloned pig embryos (633/787) exhibited a PN-like structure, which met the prerequisite to technically perform the new method. GFP fluorescence was observed in about half of the total blastocysts (21/40, 52.5%), which was comparable to classical zygote PN injection (28/41, 68.3%). In total, 478 cloned embryos injected with the GFP construct were transferred into 4 recipients and from one recipient 4 fetuses (day 68) were collected. In one of the fetuses which showed normal development, the integration of the transgene was confirmed by PCR in different tissues and organs from all three primary germ layers and placenta. The integration pattern of the transgene was mosaic (48 out of 84 single-cell colonies established from a kidney were positive for GFP DNA by PCR). Direct GFP fluorescence was observed macro- and microscopically in the fetus. Our novel strategy could be useful particularly for the generation of pigs with complex genetic modifications.
AB - Due to a rising demand of porcine models with complex genetic modifications for biomedical research, the approaches for their generation need to be adapted. In this study we describe the direct introduction of a gene construct into the pronucleus (PN)-like structure of cloned embryos as a novel strategy for the generation of genetically modified pigs, termed “nuclear injection”. To evaluate the reliability of this new strategy, the developmental ability of embryos in vitro and in vivo as well as the integration and expression efficiency of a transgene carrying green fluorescence protein (GFP) were examined. Eighty percent of the cloned pig embryos (633/787) exhibited a PN-like structure, which met the prerequisite to technically perform the new method. GFP fluorescence was observed in about half of the total blastocysts (21/40, 52.5%), which was comparable to classical zygote PN injection (28/41, 68.3%). In total, 478 cloned embryos injected with the GFP construct were transferred into 4 recipients and from one recipient 4 fetuses (day 68) were collected. In one of the fetuses which showed normal development, the integration of the transgene was confirmed by PCR in different tissues and organs from all three primary germ layers and placenta. The integration pattern of the transgene was mosaic (48 out of 84 single-cell colonies established from a kidney were positive for GFP DNA by PCR). Direct GFP fluorescence was observed macro- and microscopically in the fetus. Our novel strategy could be useful particularly for the generation of pigs with complex genetic modifications.
KW - Large-size DNA constructs
KW - Microinjection
KW - Multiple transgenic pigs
KW - Pronucleus-like structure
KW - Somatic cell nuclear transfer
UR - http://www.scopus.com/inward/record.url?scp=85006511676&partnerID=8YFLogxK
U2 - 10.1007/s11248-016-0004-z
DO - 10.1007/s11248-016-0004-z
M3 - Article
C2 - 27943082
AN - SCOPUS:85006511676
SN - 0962-8819
VL - 26
SP - 309
EP - 318
JO - Transgenic Research
JF - Transgenic Research
IS - 2
ER -