TY - JOUR
T1 - Nucleic acids delivery methods for genome editing in zygotes and embryos
T2 - The old, the new, and the old-new
AU - Sato, Masahiro
AU - Ohtsuka, Masato
AU - Watanabe, Satoshi
AU - Gurumurthy, Channabasavaiah B.
N1 - Funding Information:
MS was partially supported by a grant (no. 15K07695) from the Ministry of Education, Science, Sports, and Culture, Japan. CBG was partially supported by an Institutional Development Award (IDeA) from the National Institute of General Medical Sciences of the National Institutes of Health under grant number P20GM103471.
Publisher Copyright:
� 2016 Sato et al.
PY - 2016
Y1 - 2016
N2 - In the recent years, sequence-specific nucleases such as ZFNs, TALENs, and CRISPR/Cas9 have revolutionzed the fields of animal genome editing and transgenesis. However, these new techniques require microinjection to deliver nucleic acids into embryos to generate gene-modified animals. Microinjection is a delicate procedure that requires sophisticated equipment and highly trained and experienced technicians. Though over a dozen alternate approaches for nucleic acid delivery into embryos were attempted during the pre-CRISPR era, none of them became routinely used as microinjection. The addition of CRISPR/Cas9 to the genome editing toolbox has propelled the search for novel delivery approaches that can obviate the need for microinjection. Indeed, some groups have recently developed electroporation-based methods that have the potential to radically change animal transgenesis. This review provides an overview of the old and new delivery methods, and discusses various strategies that were attempted during the last three decades. In addition, several of the methods are re-evaluated with respect to their suitability to deliver genome editing components, particularly CRISPR/Cas9, to embryos. Reviewers: Drs. Eugene Koonin and Haruhiko Siomi.
AB - In the recent years, sequence-specific nucleases such as ZFNs, TALENs, and CRISPR/Cas9 have revolutionzed the fields of animal genome editing and transgenesis. However, these new techniques require microinjection to deliver nucleic acids into embryos to generate gene-modified animals. Microinjection is a delicate procedure that requires sophisticated equipment and highly trained and experienced technicians. Though over a dozen alternate approaches for nucleic acid delivery into embryos were attempted during the pre-CRISPR era, none of them became routinely used as microinjection. The addition of CRISPR/Cas9 to the genome editing toolbox has propelled the search for novel delivery approaches that can obviate the need for microinjection. Indeed, some groups have recently developed electroporation-based methods that have the potential to radically change animal transgenesis. This review provides an overview of the old and new delivery methods, and discusses various strategies that were attempted during the last three decades. In addition, several of the methods are re-evaluated with respect to their suitability to deliver genome editing components, particularly CRISPR/Cas9, to embryos. Reviewers: Drs. Eugene Koonin and Haruhiko Siomi.
KW - CRISPR/Cas
KW - Genome editing
KW - Mcroinjection
KW - Nucleic acids delivery
KW - Pronuclaer injection
KW - Transgenic
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U2 - 10.1186/S13062-016-0115-8
DO - 10.1186/S13062-016-0115-8
M3 - Review article
C2 - 27037013
AN - SCOPUS:85007453685
SN - 1745-6150
VL - 11
JO - Biology direct
JF - Biology direct
IS - 1
M1 - 16
ER -