Generation of functional oocytes from male mice in vitro

Nature. 2023 Mar;615(7954):900-906. doi: 10.1038/s41586-023-05834-x. Epub 2023 Mar 15.

Abstract

Sex chromosome disorders severely compromise gametogenesis in both males and females. In oogenesis, the presence of an additional Y chromosome or the loss of an X chromosome disturbs the robust production of oocytes1-5. Here we efficiently converted the XY chromosome set to XX without an additional Y chromosome in mouse pluripotent stem (PS) cells. In addition, this chromosomal alteration successfully eradicated trisomy 16, a model of Down's syndrome, in PS cells. Artificially produced euploid XX PS cells differentiated into mature oocytes in culture with similar efficiency to native XX PS cells. Using this method, we differentiated induced pluripotent stem cells from the tail of a sexually mature male mouse into fully potent oocytes, which gave rise to offspring after fertilization. This study provides insights that could ameliorate infertility caused by sex chromosome or autosomal disorders, and opens the possibility of bipaternal reproduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Down Syndrome / genetics
  • Down Syndrome / therapy
  • Female
  • Fertilization
  • Genetic Engineering* / methods
  • Homosexuality, Male
  • In Vitro Techniques*
  • Infertility / therapy
  • Male
  • Mice
  • Oocytes* / metabolism
  • Oocytes* / physiology
  • Pluripotent Stem Cells / metabolism
  • Sex Chromosome Disorders / complications
  • Sex Chromosome Disorders / genetics
  • Sex Chromosome Disorders / therapy
  • X Chromosome* / genetics
  • Y Chromosome / genetics

Supplementary concepts

  • Chromosome 16, trisomy