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Regulation of male germline transmission patterns by the Trp53-Cdkn1a pathway.
Kanatsu-Shinohara, Mito; Naoki, Honda; Tanaka, Takashi; Tatehana, Misako; Kikkawa, Takako; Osumi, Noriko; Shinohara, Takashi.
Affiliation
  • Kanatsu-Shinohara M; Department of Molecular Genetics, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan; AMED-CREST, Chiyodaku, Tokyo 100-0004, Japan.
  • Naoki H; Laboratory of Data-driven Biology, Graduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, Hiroshima, Japan.
  • Tanaka T; Department of Molecular Genetics, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan.
  • Tatehana M; Department of Developmental Neuroscience, United Centers for Advanced Research and Translational Medicine (ART), Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Kikkawa T; Department of Developmental Neuroscience, United Centers for Advanced Research and Translational Medicine (ART), Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Osumi N; Department of Developmental Neuroscience, United Centers for Advanced Research and Translational Medicine (ART), Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Shinohara T; Department of Molecular Genetics, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan. Electronic address: tshinoha@virus.kyoto-u.ac.jp.
Stem Cell Reports ; 17(9): 1924-1941, 2022 09 13.
Article in En | MEDLINE | ID: mdl-35931081
ABSTRACT
A small number of offspring are born from the numerous sperm generated from spermatogonial stem cells (SSCs). However, little is known regarding the rules and molecular mechanisms that govern germline transmission patterns. Here we report that the Trp53 tumor suppressor gene limits germline genetic diversity via Cdkn1a. Trp53-deficient SSCs outcompeted wild-type (WT) SSCs and produced significantly more progeny after co-transplantation into infertile mice. Lentivirus-mediated transgenerational lineage analysis showed that offspring bearing the same virus integration were repeatedly born in a non-random pattern from WT SSCs. However, SSCs lacking Trp53 or Cdkn1a sired transgenic offspring in random patterns with increased genetic diversity. Apoptosis of KIT+ differentiating germ cells was reduced in Trp53- or Cdkn1a-deficient mice. Reduced CDKN1A expression in Trp53-deficient spermatogonia suggested that Cdkn1a limits genetic diversity by supporting apoptosis of syncytial spermatogonial clones. Therefore, the TRP53-CDKN1A pathway regulates tumorigenesis and the germline transmission pattern.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Semen / Adult Germline Stem Cells Limits: Animals Language: En Journal: Stem Cell Reports Year: 2022 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Semen / Adult Germline Stem Cells Limits: Animals Language: En Journal: Stem Cell Reports Year: 2022 Document type: Article Affiliation country: Japan