| Literature DB >> 30318303 |
Zhi-Kun Li1, Le-Yun Wang1, Li-Bin Wang2, Gui-Hai Feng1, Xue-Wei Yuan3, Chao Liu2, Kai Xu2, Yu-Huan Li2, Hai-Feng Wan1, Ying Zhang1, Yu-Fei Li2, Xin Li1, Wei Li4, Qi Zhou5, Bao-Yang Hu6.
Abstract
Unisexual reproduction is widespread among lower vertebrates, but not in mammals. Deletion of the H19 imprinted region in immature oocytes produced bimaternal mice with defective growth; however, bipaternal reproduction has not been previously achieved in mammals. We found that cultured parthenogenetic and androgenetic haploid embryonic stem cells (haESCs) display DNA hypomethylation resembling that of primordial germ cells. Through MII oocyte injection or sperm coinjection with hypomethylated haploid ESCs carrying specific imprinted region deletions, we obtained live bimaternal and bipaternal mice. Deletion of 3 imprinted regions in parthenogenetic haploid ESCs restored normal growth of fertile bimaternal mice, whereas deletion of 7 imprinted regions in androgenetic haploid ESCs enabled production of live bipaternal mice that died shortly after birth. Phenotypic analyses of organ and body size of these mice support the genetic conflict theory of genomic imprinting. Taken together, our results highlight the factors necessary for crossing same-sex reproduction barriers in mammals.Entities:
Keywords: DNA hypomethylation; bimaternal mice; bipaternal mice; conflict theory; genomic imprinting; haploid embryonic stem cell; uniparental reproduction barrier
Mesh:
Year: 2018 PMID: 30318303 DOI: 10.1016/j.stem.2018.09.004
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633