Molecular mechanisms utilized by alternative c-kit gene products in the control of spermatogonial proliferation and sperm-mediated egg activation

Pellegrino Rossi, S. Dolci, C. Sette, R. Geremia

Research output: Contribution to journalArticle

35 Citations (Scopus)

Abstract

The c-kit proto-oncogene plays a dual role in the control of male fertility in mice through two alternative gene products: (1) c-kit [the transmembrane tyrosine kinase receptor for stem cell factor (SCF)], which is expressed and functional in differentiating spermatogonia of the postnatal testis, in which c-kit is essential for pre-meiotic proliferation; and (2) tr-kit, an intracellular protein which is specifically accumulated during spermiogenesis through the use of an alternative intronic promoter, and which is able to trigger mouse egg activation when microinjected into the cytoplasm of metaphase II arrested oocytes. Here, we summarize the most recent findings about the molecular pathways through which c-kit regulates cell cycle progression in mitotic germ cells, and those through which sperm-derived tr-kit triggers parthenogenetic completion of meiosis II and pronuclear formation in microinjected mouse eggs.

Original languageEnglish
Pages (from-to)71-78
Number of pages8
JournalAndrologia
Volume35
Issue number1
DOIs
Publication statusPublished - Feb 2003

Fingerprint

Ovum
Spermatozoa
Genes
Spermatogonia
Stem Cell Factor
Proto-Oncogenes
Meiosis
Receptor Protein-Tyrosine Kinases
Spermatogenesis
Metaphase
Contraception
Germ Cells
Eggs
Oocytes
Testis
Cell Cycle
Cytoplasm
Proteins

Keywords

  • c-kit
  • Cell cycle
  • Egg activation
  • Fertilization
  • Spermatogenesis
  • Spermatogonia
  • Stem cell factor
  • Tyrosine kinases

ASJC Scopus subject areas

  • Nephrology
  • Endocrinology

Cite this

Molecular mechanisms utilized by alternative c-kit gene products in the control of spermatogonial proliferation and sperm-mediated egg activation. / Rossi, Pellegrino; Dolci, S.; Sette, C.; Geremia, R.

In: Andrologia, Vol. 35, No. 1, 02.2003, p. 71-78.

Research output: Contribution to journalArticle

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