Laser-assisted Cytoplasmic Microinjection in Livestock Zygotes

被引:18
作者
Bogliotti, Yanina S. [1 ]
Vilarino, Marcela [1 ]
Ross, Pablo J. [1 ]
机构
[1] Univ Calif Davis, Dept Anim Sci, Davis, CA 95616 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2016年 / 116期
关键词
Genetics; Issue; 116; Cytoplasmic microinjection; laser; zygote; bovine; ovine; gene disruption; genome editing;
D O I
10.3791/54465
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cytoplasmic microinjection into one-cell embryos is a very powerful technique. As an example, it enables the delivery of genome editing tools that can create genetic modifications that will be present in every cell of an adult organism. It can also be used to deliver siRNA, mRNAs or blocking antibodies to study gene function in preimplantation embryos. The conventional technique for microinjecting embryos used in rodents consists of a very thin micropipette that directly penetrates the plasma membrane when advanced into the embryo. When this technique is applied to livestock animals it usually results in low efficiency. This is mainly because in contrast to mice and rats, bovine, ovine, and porcine zygotes have a very dark cytoplasm and a highly elastic plasma membrane that makes visualization during injection and penetration of the plasma membrane hard to achieve. In this protocol, we describe a suitable microinjection method for the delivery of solutions into the cytoplasm of cattle zygotes that has proved to be successful for sheep and pig embryos as well. First, a laser is used to create a hole in the zona pellucida. Then a blunt-end glass micropipette is introduced through the hole and advanced until the tip of the needle reaches about 3/4 into the embryo. Then, the plasma membrane is broken by aspiration of cytoplasmic content inside the needle. Finally, the aspirated cytoplasmic content followed by the solution of interest is injected back into the embryonic cytoplasm. This protocol has been successfully used for the delivery of different solutions into bovine and ovine zygotes with 100% efficiency, minimal lysis, and normal blastocysts development rates.
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页数:7
相关论文
共 11 条
[1]   DPPA3 prevents cytosine hydroxymethylation of the maternal pronucleus and is required for normal development in bovine embryos [J].
Bakhtari, Azizollah ;
Ross, Pablo J. .
EPIGENETICS, 2014, 9 (09) :1271-1279
[2]  
Bogliotti Y.S., 2015, Reproduction, Fertility and Development, V27, DOI DOI 10.1071/RDV27N1AB4
[3]   FACTORS AFFECTING THE EFFICIENCY OF INTRODUCING FOREIGN DNA INTO MICE BY MICROINJECTING EGGS [J].
BRINSTER, RL ;
CHEN, HY ;
TRUMBAUER, ME ;
YAGLE, MK ;
PALMITER, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (13) :4438-4442
[4]   Jumonji domain-containing protein 3 regulates histone 3 lysine 27 methylation during bovine preimplantation development [J].
Canovas, Sebastian ;
Cibelli, Jose B. ;
Ross, Pablo J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (07) :2400-2405
[5]  
Cibelli JB, 2002, PRINCIPLES CLONING
[6]   Fatty acid composition of lipids in immature cattle, pig and sheep oocytes with intact zona pellucida [J].
McEvoy, TG ;
Coull, GD ;
Broadbent, PJ ;
Hutchinson, JSM ;
Speake, BK .
JOURNAL OF REPRODUCTION AND FERTILITY, 2000, 118 (01) :163-170
[7]  
Ross P. J., BMC DEV BIOL, V8, P16
[8]  
Sutter Instrument, 2014, P 97 FLAM BROWN TM M
[9]  
Sutter Instrument, 2015, PIP COOKB 2015 P 97
[10]  
Wang B, 2001, MOL REPROD DEV, V60, P433, DOI 10.1002/mrd.1107