Totipotency of mouse zygotes extends to single blastomeres of embryos at the four-cell stage

被引:0
|
作者
Marino Maemura
Hiroaki Taketsuru
Yuki Nakajima
Ruiqi Shao
Ayaka Kakihara
Jumpei Nogami
Yasuyuki Ohkawa
Yu-ichi Tsukada
机构
[1] Kyushu University,Graduate School of Systems Life Sciences
[2] INAMORI Frontier Research Center,Advanced Biological Information Research Division
[3] Kyushu University,Division of Transcriptomics
[4] Medical Institute of Bioregulation,undefined
[5] Kyushu University,undefined
来源
Scientific Reports | / 11卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
In multicellular organisms, oocytes and sperm undergo fusion during fertilization and the resulting zygote gives rise to a new individual. The ability of zygotes to produce a fully formed individual from a single cell when placed in a supportive environment is known as totipotency. Given that totipotent cells are the source of all multicellular organisms, a better understanding of totipotency may have a wide-ranging impact on biology. The precise delineation of totipotent cells in mammals has remained elusive, however, although zygotes and single blastomeres of embryos at the two-cell stage have been thought to be the only totipotent cells in mice. We now show that a single blastomere of two- or four-cell mouse embryos can give rise to a fertile adult when placed in a uterus, even though blastomere isolation disturbs the transcriptome of derived embryos. Single blastomeres isolated from embryos at the eight-cell or morula stages and cultured in vitro manifested pronounced defects in the formation of epiblast and primitive endoderm by the inner cell mass and in the development of blastocysts, respectively. Our results thus indicate that totipotency of mouse zygotes extends to single blastomeres of embryos at the four-cell stage.
引用
收藏
相关论文
共 50 条
  • [41] Expression of DNA Methyltransferase Genes in Four-Cell Bovine Embryos Cultured in the Presence of Oviductal Fluid
    Barrera, D.
    Garcia, E. V.
    Sinowatz, F.
    Palma, G. A.
    Jimenez-Diaz, M. A.
    Miceli, D. C.
    ANATOMIA HISTOLOGIA EMBRYOLOGIA, 2013, 42 (04) : 312 - 315
  • [42] Influence of oocyte aging on developmental ability of reconstituted embryos produced from oocyte cytoplast and single blastomeres of two-cell stage embryos
    Taniguchi, T
    Taniguchi, R
    Kanagawa, H
    JOURNAL OF VETERINARY MEDICAL SCIENCE, 1996, 58 (07): : 635 - 640
  • [43] INVITRO DEVELOPMENT OF HALF-EMBRYOS AND CHIMERAS RECONSTRUCTED FROM FROZEN THAWED BLASTOMERES ISOLATED FROM 8-CELL STAGE MOUSE EMBRYOS
    LANDA, V
    AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY AND MICROBIOLOGY, 1985, 7 (02): : 83 - 83
  • [44] Esrrb-Cre excises loxP-flanked alleles in early four-cell embryos
    Lee, Sungeun
    Pallerla, Srinivas R.
    Kim, Suyeon
    Shaffer, Benjamin
    Simerly, Calvin R.
    Chaillet, J. Richard
    Barak, Yaacov
    GENESIS, 2016, 54 (01) : 53 - 61
  • [45] The effect of superovulation on the contributions of individual blastomeres from 2-cell stage CF1 mouse embryos to the blastocyst
    Katayama, Mika
    Roberts, R. Michael
    INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY, 2010, 54 (04): : 675 - 681
  • [46] CARM1 is heterogeneous in mouse four-cell embryo and important to blastocyst development
    Sun, Hongzheng
    Su, Jianmin
    Wu, Teng
    Wang, Fengyu
    Kang, Jian
    Zhang, Jingcheng
    Xing, Xupeng
    Cheng, Yuyao
    Zhang, Yong
    REPRODUCTION, 2020, 159 (01) : 91 - 104
  • [47] DEVELOPMENT OF SINGLE BLASTOMERES DERIVED FROM PORCINE TWO-CELL EMBRYOS
    Dang-Nguyen, T. Q.
    Kaneda, M.
    Somfai, T.
    Akagi, S.
    Nakai, M.
    Kikuchi, K.
    Kanai, Y.
    Nagai, T.
    REPRODUCTION FERTILITY AND DEVELOPMENT, 2010, 22 (01) : 222 - 222
  • [48] DEVELOPMENTAL FATES OF BLASTOMERES OF 8-CELL-STAGE XENOPUS-LAEVIS EMBRYOS
    MASHO, R
    KUBOTA, HY
    DEVELOPMENT GROWTH & DIFFERENTIATION, 1986, 28 (02) : 113 - 123
  • [50] EVALUATION OF DIFFERENT BIOPSY METHODS OF BLASTOMERES FROM 2-CELL MOUSE EMBRYOS
    NIJS, M
    CAMUS, M
    VANSTEIRTEGHEM, AC
    HUMAN REPRODUCTION, 1988, 3 (08) : 999 - 1003