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TCL1 participates in early embryonic development and is overexpressed in human seminomas.

Overexpression of the TCL1 oncogene has been shown to play a causative role in T cell leukemias of humans and mice. The characterization of Tcl1-deficient mice in these studies indicates an important developmental role for Tcl1 in early embryogenesis. In wild-type embryos, Tcl1 is abundant in the first three mitotic cycles, during which it shuttles between nuclei and the embryo cortical regions in a cell-cycle-dependent fashion. The absence of this protein in early embryogenesis results in reduced fertility of female mice. The present studies elucidate the mechanism responsible for the reduced female fertility through analysis of the oogenesis stages and early embryo development in Tcl1-deficient mice. Even though Tcl1(-/-) females display normal oogenesis and rates of oocyte maturation/ovulation and fertilization, the lack of maternally derived Tcl1 impairs the embryo's ability to undergo normal cleavage and develop to the morula stage, especially under in vitro culture conditions. Beyond this crisis point, differentiative traits of zygotic genome activation and embryo compaction can take place normally. In contrast with this unanticipated role in early embryogenesis, we observed an overexpression of TCL1 in human seminomas. This finding suggests that TCL1 dysregulation could contribute to the development of this germinal cell cancer as well as lymphoid malignancies.

Pubmed ID: 12181493

Authors

  • Narducci MG
  • Fiorenza MT
  • Kang SM
  • Bevilacqua A
  • Di Giacomo M
  • Remotti D
  • Picchio MC
  • Fidanza V
  • Cooper MD
  • Croce CM
  • Mangia F
  • Russo G

Journal

Proceedings of the National Academy of Sciences of the United States of America

Publication Data

September 3, 2002

Associated Grants

  • Agency: NIAID NIH HHS, Id: AI39816
  • Agency: NCI NIH HHS, Id: CA76259
  • Agency: Telethon, Id: D.102

Mesh Terms

  • Animals
  • Base Sequence
  • Blastomeres
  • DNA Primers
  • DNA-Binding Proteins
  • Embryonic Development
  • Embryonic and Fetal Development
  • Female
  • Gene Expression Regulation, Developmental
  • Infertility, Female
  • Mice
  • Mice, Knockout
  • Pregnancy
  • Proto-Oncogene Proteins
  • Seminoma
  • Transcription Factors