| Literature DB >> 29395327 |
Zhen Liu1, Yijun Cai1, Yan Wang1, Yanhong Nie1, Chenchen Zhang1, Yuting Xu1, Xiaotong Zhang1, Yong Lu1, Zhanyang Wang1, Muming Poo1, Qiang Sun2.
Abstract
Generation of genetically uniform non-human primates may help to establish animal models for primate biology and biomedical research. In this study, we have successfully cloned cynomolgus monkeys (Macaca fascicularis) by somatic cell nuclear transfer (SCNT). We found that injection of H3K9me3 demethylase Kdm4d mRNA and treatment with histone deacetylase inhibitor trichostatin A at one-cell stage following SCNT greatly improved blastocyst development and pregnancy rate of transplanted SCNT embryos in surrogate monkeys. For SCNT using fetal monkey fibroblasts, 6 pregnancies were confirmed in 21 surrogates and yielded 2 healthy babies. For SCNT using adult monkey cumulus cells, 22 pregnancies were confirmed in 42 surrogates and yielded 2 babies that were short-lived. In both cases, genetic analyses confirmed that the nuclear DNA and mitochondria DNA of the monkey offspring originated from the nucleus donor cell and the oocyte donor monkey, respectively. Thus, cloning macaque monkeys by SCNT is feasible using fetal fibroblasts.Entities:
Keywords: Genetic editing; Human disease models; Macaque monkey cloning; Non-human primates; Somatic cell nuclear transfer; cumulus cells; epigenetic modulators; fetal fibroblasts; primate neurobiology; reprogramming
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Year: 2018 PMID: 29395327 DOI: 10.1016/j.cell.2018.01.020
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582