Noninvasive visualization of molecular events in the mammalian zygote
Version of Record online: 12 AUG 2005
Copyright © 2005 Wiley-Liss, Inc.
Volume 43, Issue 2, pages 71–79, October 2005
How to Cite
Yamagata, K., Yamazaki, T., Yamashita, M., Hara, Y., Ogonuki, N. and Ogura, A. (2005), Noninvasive visualization of molecular events in the mammalian zygote. Genesis, 43: 71–79. doi: 10.1002/gene.20158
- Issue online: 7 SEP 2005
- Version of Record online: 12 AUG 2005
- Manuscript Accepted: 16 JUL 2005
- Manuscript Received: 1 APR 2005
- one-cell zygote;
- preimplantation development;
- fluorescence imaging;
- DNA methylation;
- spindle formation
Following fertilization, a number of molecular events are triggered in the mammalian zygote. As biochemical studies using mammalian gametes and zygotes have inherent difficulties, the molecular nature of these processes is currently unclear. We have developed a method to visualize these events. In vitro transcribed mRNAs encoding for proteins fused with green fluorescent protein were microinjected into oocytes or embryos and fluorescence signals were observed. Using this technique we succeeded in obtaining images of the DNA methylation status in living mouse and rabbit embryos. Moreover, time-lapse images were acquired of spindle and nuclear formation during second meiosis and first mitosis. Importantly, the microinjected embryos developed to the normal offspring even after observation, suggesting that the technique is relatively noninvasive. Thus, our method may help elucidate the molecular aspects of fertilization and preimplantation development and, based on the real-time genetic and epigenetic status, could become a tool to select “good quality” embryos before implantation. genesis 43:71–79, 2005. © 2005 Wiley-Liss, Inc.