Msx1 and Msx2 promote meiosis initiation

Author:

Le Bouffant Ronan123,Souquet Benoit123,Duval Nathalie4,Duquenne Clotilde123,Hervé Roxane123,Frydman Nelly56,Robert Benoit4,Habert René123,Livera Gabriel123

Affiliation:

1. CEA, DSV/iRCM/SCSR/LDG, Laboratoire de Développement des Gonades, Unité Cellules Souches et Radiation, F-92265 Fontenay aux Roses, France.

2. Univ Paris Diderot, Sorbonne Paris Cité, LDG, UMR-967, F-92265 Fontenay aux Roses, France.

3. INSERM, U967, F-92265 Fontenay aux Roses, France.

4. CNRS URA2578, Génétique Moléculaire de la Morphogenèse, Institut Pasteur, Paris, France.

5. Université Paris-Sud, Clamart, F-92140, AP-HP, Service de Gynécologie-Obstétrique et Médecine de la Reproduction, Hôpital Antoine Béclère, F-92140 Clamart, France.

6. INSERM, U782, F-92140 Clamart, France.

Abstract

The mechanisms regulating germ line sex determination and meiosis initiation are poorly understood. Here, we provide evidence for the involvement of homeobox Msx transcription factors in foetal meiosis initiation in mammalian germ cells. Upon meiosis initiation, Msx1 and Msx2 genes are strongly expressed in the foetal ovary, possibly stimulated by soluble factors found there: bone morphogenetic proteins Bmp2 and Bmp4, and retinoic acid. Analysis of Msx1/Msx2 double mutant embryos revealed a majority of undifferentiated germ cells remaining in the ovary and, importantly, a decrease in the number of meiotic cells. In vivo, the Msx1/Msx2 double-null mutation prevented full activation of Stra8, a gene required for meiosis. In F9 cells, Msx1 can bind to Stra8 regulatory sequences and Msx1 overexpression stimulates Stra8 transcription. Collectively, our data demonstrate for the first time that some homeobox genes are required for meiosis initiation in the female germ line.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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