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Mice deficient for the wild-type p53-induced phosphatase gene (Wip1) exhibit defects in reproductive organs, immune function, and cell cycle control.

The Wip1 gene is a serine/threonine phosphatase that is induced in a p53-dependent manner by DNA-damaging agents. We show here that Wip1 message is expressed in moderate levels in all organs, but is present at very high levels in the testes, particularly in the postmeiotic round spermatid compartment of the seminiferous tubules. We have confirmed that Wip1 mRNA is induced by ionizing radiation in mouse tissues in a p53-dependent manner. To further determine the normal biological function of Wip1 in mammalian organisms, we have generated Wip1-deficient mice. Wip1 null mice are viable but show a variety of postnatal abnormalities, including variable male runting, male reproductive organ atrophy, reduced male fertility, and reduced male longevity. Mice lacking Wip1 show increased susceptibility to pathogens and diminished T- and B-cell function. Fibroblasts derived from Wip1 null embryos have decreased proliferation rates and appear to be compromised in entering mitosis. The data are consistent with an important role for Wip1 in spermatogenesis, lymphoid cell function, and cell cycle regulation.

Pubmed ID: 11809801


  • Choi J
  • Nannenga B
  • Demidov ON
  • Bulavin DV
  • Cooney A
  • Brayton C
  • Zhang Y
  • Mbawuike IN
  • Bradley A
  • Appella E
  • Donehower LA


Molecular and cellular biology

Publication Data

February 25, 2002

Associated Grants

  • Agency: NCI NIH HHS, Id: CA54897

Mesh Terms

  • Animals
  • B-Lymphocytes
  • Body Constitution
  • Cell Cycle
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • Embryonic and Fetal Development
  • Female
  • Gene Expression Regulation
  • Gene Targeting
  • Humans
  • Immune System
  • In Situ Hybridization
  • Kidney
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neoplasm Proteins
  • Phosphoprotein Phosphatases
  • RNA, Messenger
  • Radiation, Ionizing
  • Reproduction
  • Spermatogenesis
  • Spleen
  • Stem Cells
  • T-Lymphocytes
  • Testis