TY - JOUR
T1 - Generation of functional oocytes from male mice in vitro
AU - Murakami, Kenta
AU - Hamazaki, Nobuhiko
AU - Hamada, Norio
AU - Nagamatsu, Go
AU - Okamoto, Ikuhiro
AU - Ohta, Hiroshi
AU - Nosaka, Yoshiaki
AU - Ishikura, Yukiko
AU - Kitajima, Tomoya S.
AU - Semba, Yuichiro
AU - Kunisaki, Yuya
AU - Arai, Fumio
AU - Akashi, Koichi
AU - Saitou, Mitinori
AU - Kato, Kiyoko
AU - Hayashi, Katsuhiko
N1 - Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2023/3/30
Y1 - 2023/3/30
N2 - 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.
AB - 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.
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U2 - 10.1038/s41586-023-05834-x
DO - 10.1038/s41586-023-05834-x
M3 - Article
C2 - 36922585
AN - SCOPUS:85149959936
SN - 0028-0836
VL - 615
SP - 900
EP - 906
JO - Nature
JF - Nature
IS - 7954
ER -