Department of Biological Sciences, Graduate School of Science, The University of Tokyo

Department of Biological Sciences
Graduate School of Science
The University of Tokyo

Labs Ohsugi Lab

JP

Core Division / Biology Ohsugi Lab

Laboratory Website

Professor Miho Ohsugi

Associate Professor Masatoshi Hara

Assistant Professor Tomo Kondo

Assistant Professor Ryohei Nakamura

Subject of research

  1. 1. Decoding the unique mechanisms of cell division during oocyte meiosis and early cleavage in mammals
  2. 2. Investigating how genome ploidy and cell size influence mammalian embryonic development
  3. 3. Understanding the mechanisms of cytoplasmic flow generation and organelle positioning in mouse oocytes
  4. 4. Developing new methods to manipulate mouse embryos by targeting the cell division machinery.

Elucidating Mammal-Specific Mechanisms of Fertilization and Embryonic Development

A totipotent zygote is created when sperm and oocyte fuse in the process of fertilization. This zygote then undergoes a specialized form of cell division called cleavage, gradually differentiating and progressing through embryonic development. Although this process shares universal features across species, it also exhibits unexpected diversity. It has become clear that mammals, in which fertilization and development occur entirely within the female body, exhibit many differences from other vertebrates.
Our laboratory focuses on investigating these mammal-specific features of fertilization and early development. We explore how organelle positioning, such as that of the spindle, is controlled during the ~2-hour period following sperm–egg fusion that culminates in zygote formation.
We also examine why chromosome missegregation and aneuploidy frequently occur during cleavage-stage divisions, and why mammalian embryos are particularly sensitive to changes in ploidy.
Using live imaging and other cell biological approaches, we aim to understand these processes at the molecular level and shed light on the unique aspects of mammalian embryogenesis.
 
  • Mouse 2-cell embryo with maternal and paternal chromosomes differentially stained