image: Immunostained proteins SYCP3 (green) and DAZL (red) in embryonic ovaries of a control mouse (left); a mouse with mutant null Aldh1a1, Aldh1a2, and Aldh1a3 alleles (centre); and a mouse with mutant null retinoic acid receptor gene alleles (right). In all three situations, germ cells (red) have entered meiosis, as evidenced by the presence of SYCP3 on meiotic chromosomes (green). view more
Credit: Anne-Amandine Chassot and Norbert B. Ghyselinck
Meiosis is essential to sexual reproduction. For almost 15 years, it has been commonly held that retinoic acid, a molecule derived from vitamin A, triggers meiosis in mammalian germ cells. Yet, in joint articles published in Science Advances ( 22 May 2020 ), french researchers from the Institut de Biologie Valrose (CNRS / INSERM / Université Côte d'Azur) and the IGBMC (CNRS / INSERM / University of Strasbourg), with their colleagues, demonstrate that meiosis in mice begins and proceeds normally even in the absence of retinoic acid. These findings set the stage for new research in the field of reproductive biology.
Meiosis is an essential process that results in novel assortments of chromosomes for the transmission of unique sets of genes to offspring. Beginning with a diploid[1] germ cell (an oogonium in females or a spermatogonium in males), it yields haploid[2] gametes (oocytes in females or spermatozoa in males). The union of an oocyte and a spermatozoon combines both parental haploid genomes in a single diploid cell destined to give rise to an embryo, marking the start of the next generation.
In mammals, cells found in developing gonads (ovaries in females or testes in males) provide germ cells with structural support, nourishment, and protection. They also emit molecular signals that determine what will become of the germ cells. One of the signalling molecules is retinoic acid, widely thought to trigger germ cell meiosis. Despite the 2011 publication of findings casting doubt on this assumption, the idea that retinoic acid is a switch for meiosis has risen to the status of dogma.
Together with colleagues,[3] scientists from the Institut de Biologie Valrose in Nice and the IGBMC in Strasbourg conducted two complementary studies of the mouse foetal ovary to clarify the role of this molecule, by (i) inhibiting its synthesis and (ii) removing its receptors. Neither approach prevented normal initiation of meiosis in germ cells. Furthermore, viable infant mice were born after fertilization of oocytes lacking retinoic acid receptors, proving that these cells are functionally intact.
These twin studies therefore refute the dogma of a retinoic acid trigger for meiosis in germ cells, ending a debate that has lasted nearly a decade and a half. By dismissing a long-held tenet, these findings invite the scientific community to reconsider its working assumptions and investigate new leads in the search for the real signals controlling initiation of germ cell meiosis.
###
Notes
- 1. In diploid cells, there are two sets of chromosomes, representing pairs of maternal and paternal alleles.
2. In haploid cells, there is only one set of chromosomes.
3. This work also involved male and female scientists from the Department of Reproductive Biology of the Strasbourg Teaching Hospital Network (HUS: Hôpitaux Universitaires de Strasbourg); the Biologie de la Reproduction, Environnement, Épigénétique, et Développement (BREED) research laboratory (INRAE / Université Paris-Saclay / ENVA); the University of Geneva; and the German Cancer Research Center.
Bibliography
Retinoic Acid synthesis by ALDH1A proteins is dispensable for meiosis initiation in the mouse fetal ovary. Anne Amandine Chassot, Morgane Le Rolle, Geneviève Jolivet, Isabelle Stevant, Jean-Marie Guigonis Fabio Da Silva, Serge Nef, Eric Pailhoux, Andreas Schedl, Norbert B. Ghyselinck and Marie-Christine Chaboissier. Science Advances, May 22, 2020. DOI : 10.1126/sciadv.aaz1261
Meiosis occurs normally in the fetal ovary of mice lacking all retinoic acid receptors. Nadège Vernet, Diana Condrea, Chloé Mayere, Betty Féret, Muriel Klopfenstein, William Magnant, Violaine Alunni, Marius Teletin, Sirine Souali-Crespo, Serge Nef, Manuel Mark, and Norbert B. Ghyselinck. Science Advances, May 22, 2020. DOI : 10.1126/sciadv.aaz1139.
Journal
Science Advances