Although somatic cell nuclear transfer (SCNT) is frequently employed to produce
cloned animals in laboratories, this technique is expensive and inefficient.
Therefore, the handmade cloning (HMC) technique has been suggested to simplify
and advance the cloning process, however, HMC wastes many oocytes and leads to
mitochondrial heteroplasmy. To solve these problems, we propose a modified
handmade cloning (mHMC) technique that uses simple laboratory equipment, i.e., a
Pasteur pipette and an alcohol lamp, applying it to porcine embryo cloning. To
validate the application of mHMC to pig cloning, embryos produced through SCNT
and mHMC are compared using multiple methods, such as enucleation efficiency,
oxidative stress, embryo developmental competence, and gene expression. The
results show no significant differences between techniques except in the
enucleation efficiency. The 8-cell and 16-cell embryo developmental competence
and Oct4 expression levels exhibit significant differences. However, the
blastocyst rate is not significantly different between mHMC and SCNT. This study
verifies that cloned embryos derived from the two techniques exhibit similar
generation and developmental competence. Thus, we suggest that mHMC could
replace SCNT for simpler and cheaper porcine cloning.