𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Efficient production of androgenetic embryos by round spermatid injection

✍ Scribed by Hiromi Miki; Michiko Hirose; Narumi Ogonuki; Kimiko Inoue; Fuyuko Kezuka; Arata Honda; Kazuyuki Mekada; Ken-Ichi Hanaki; Hirotaka Iwafune; Atsushi Yoshiki; Fumitoshi Ishino; Atsuo Ogura


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
326 KB
Volume
47
Category
Article
ISSN
1526-954X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Mammalian androgenetic embryos can be produced by pronuclear exchange of fertilized oocytes or by dispermic in vitro fertilization of enucleated oocytes. Here, we report a new technique for producing mouse androgenetic embryos by injection of two round spermatid nuclei into oocytes, followed by female chromosome removal. We found that injection of round spermatids resulted in high rates of oocyte survival (88%). Androgenetic embryos thus produced developed into mid‐gestation fetuses at various rates, depending on the mouse strain used. All the fetuses examined maintained paternally specific genomic imprinting memories. This technique also enabled us to produce complete heterozygous F1 embryos by injecting two spermatids from different strains. The best rate of fetal survival (12% per embryos transferred) was obtained with C57BL/6 × DBA/2 androgenetic embryos. We also generated embryonic stem cell lines efficiently with the genotype of Mus musculus domesticus × M. m. molossinus. Thus, injection of two round spermatid nuclei followed by maternal enucleation is an effective alternative method of producing androgenetic embryos that consistently develop into blastocysts and mid‐gestation fetuses. genesis 47:155–160, 2009. © 2009 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Efficient production of transgenic cattl
✍ R. E. Haskell; R. A. Bowen 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 633 KB

## Abstract Production of transgenic cattle by microinjection of DNA has been difficult and costly. To explore an alternative method, one‐ to four‐cell bovine embryos were exposed to a replication‐defective retrovirus by microinjection of retrovirus producer cells into the perivitelline space. Embr