Press releases

Beginning of life: how does symmetry come into play?

04 Jan 2016 | By Inserm (Newsroom) | Cell biology, development and evolution

The first embryonic division, which follows gamete fusion (oocyte and spermatozoon), starts the development of a new individual, the genesis of a functional adult body. This division is symmetric in the one-cell embryo stage (also known as the zygote); it leads to the formation of two daughter cells of identical size. Conversely, it is asymmetric in the oocyte, which has the same size and shape as the zygote. Why? What directs the zygote to divide symmetrically, while the oocyte divides asymmetrically during meiosis? Such are the questions pondered by Marie-Emilie Terret, a researcher at Inserm, and Marie-Hélène Verlhac, a researcher at CNRS and director of the Asymmetric Divisions in Oocytes team at the Center for Interdisciplinary Research in Biology (CIRB; Inserm/CNRS/Collège de France)[1]. By combining biology, physics and mathematics, the researchers succeeded in demonstrating, in mice, the regulatory mechanics that determine, in a very short time, the geometry and hence the fate (symmetric or asymmetric division) of the cell. In future, the elements arising from this work may contribute to improving the efficacy of in vitro fertilisation.

Details of these results are published today in the journal Nature communications.


At the one-cell stage, the embryo very closely resembles an oocyte: a round, isolated cell, similar in size to an oocyte. The geometry of a cell’s division is determined by the position of the microtubule spindle, the machinery that carries and separates the chromosomes. In most animal cells, the centrosomes organise the microtubule network, which is essential to the formation and positioning of the division spindle. But oocytes and zygotes lack centrosomes. A major difference between these two types of cells, however, lies in the geometry of their divisions. Indeed, during meiosis oocytes divide in an extremely asymmetric manner in terms of size, allowing the formation of a single enormous oocyte and the expulsion of “polar bodies” containing the excess genetic material. Conversely, the zygote divides in a perfectly symmetric manner, leading to the formation of two daughter cells of identical size.

CP Terret

Mouse oocyte and embryo at the one-cell stage. The top images show the actin networks; the bottom images show the microtubule spindles with aligned chromosomes.

(c) Marie-Emilie Terret

The geometry of division is determined by the position of the spindle: eccentric in oocytes, centred in zygotes. The Asymmetric Divisions in Oocytes team had previously shown that the eccentric position of the division spindle in the oocyte depends on the mechanics of the actin networks. In the work published today, the team of researchers shows that the centred position of the division spindle in the zygote is also due to the mechanics of the actin networks, but controlled differently.

Three steps are required for this symmetric division:

  1. The coarse centring of the male and female pronuclei, requiring a network of actin and myosin-Vb.
  2. The fine centring of the division spindle, requiring strong rigidity in the oocyte.
  3. The passive maintenance of the spindle in the centre of the cell.

The mechanics of actin/myosin networks therefore make it possible to change from an asymmetric division to a symmetric division, a change in geometry needed for the transition from oocyte to embryo.


The research team is already formulating hypotheses regarding the mode of action of actin, which plays a role in the physical characteristics of the cell membrane (rigid or soft), which in turn influence the geometry of division. “Our next work will involve the more detailed study of interactions between actin and microtubules in an attempt to understand their respective roles in the architecture of the cell at the moment of division, and the potential involvement of other intermediary proteins,” explains Marie-Emilie Terret.

A better understanding of the physical characteristics and behaviour of the oocyte during division, whether fertilised or not, has the potential to contribute useful new elements to medically assisted conception. During in vitro fertilisation (IVF), for instance, the storage temperature of the oocytes can have an impact on the quality of the actin networks, and consequently affect division, and hence the formation of a zygote.

Increasing the efficacy of IVF might therefore represent a long-term objective for this research team, one of the few in France working on this theme.

[1] In collaboration with researchers from the Laboratory for Analysis and Modelling for Biology and Environment (LAMBE; CNRS/CEA/University of Évry Val d’Essonne/Cergy Pontoise University), the Theoretical Physics of Condensed Matter Laboratory (LPTMC; CNRS/UPMC) and the Curie Physical Chemistry Laboratory (CNRS/Institut Curie/UPMC).

Researcher Contact
Marie-Emilie Terret Chargée de recherche Inserm Centre interdisciplinaire de recherche en biologie (Inserm/CNRS/Collège de France) rf.ecnarf-ed-egelloc@terret.eilime-eiram 01 44 27 16 92
Marie-Hélène Verlhac Directrice de recherche CNRS Centre interdisciplinaire de recherche en biologie (Inserm/CNRS/Collège de France) rf.ecnarf-ed-egelloc@cahlrev.eneleh-eiram 01 44 27 10 82
Press Contact
“F-actin mechanics control spindle centring in the mouse zygote” Agathe Chaigne 1,w, Clément Campillo 2, Raphaël Voituriez 3,*, Nir S. Gov 4,*, Cécile Sykes 5,6,7, Marie-Hélène Verlhac1 & Marie-Emilie Terret 1 1 CIRB, Collège de France, and CNRS-UMR7241 and INSERM-U1050, Equipe labellisée Ligue contre le Cancer, Paris F-75005, France. 2 Université Evry Val d’Essonne, LAMBE, Boulevard F Mitterrand, Evry 91025, France. 3 UMR7600-CNRS/UPMC, 4 Place Jussieu, Paris F-75005, France. 4 Department of Chemical Physics, Weizmann Institute of Science, Rehovot 76100, Israel. 5 CNRS-UMR168, Paris F-75248, France. 6 UPMC, 4 Place Jussieu, Paris F-75248, France. 7 Institut Curie, Centre de Recherche, Laboratoire Physico-Chimie, Paris F-75248, France. w Present address: Laboratory for Molecular Cell Biology,UCL, London WC1E 6BT, UK. * These authors contributed equally to this work. Nature communications, 4 janvier 2016