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      Gene targeting of Desrt, a novel ARID class DNA-binding protein, causes growth retardation and abnormal development of reproductive organs.

      Genome research
      AT Rich Sequence, genetics, Adrenal Glands, abnormalities, Amino Acid Sequence, Animals, Base Sequence, Binding Sites, DNA-Binding Proteins, chemistry, Female, Gene Targeting, methods, Genitalia, Female, growth & development, Genitalia, Male, Growth Disorders, Humans, Immune System, Male, Mice, Mice, Inbred BALB C, Mice, Inbred Strains, Molecular Sequence Data, Mutation, Peptide Fragments, Sequence Homology, Nucleic Acid, Transcription Factors

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          Abstract

          We have cloned and characterized a novel murine DNA-binding protein Desrt, with a motif characteristic of the ARID (A-T rich interaction domain) family of transcription factors. The Desrt gene encodes an 83-kD protein that is shown to bind DNA and is widely expressed in adult tissues. To examine the in vivo function of Desrt, we have generated mice with a targeted mutation in the ARID domain of Desrt. Homozygous mutants have reduced viability, pronounced growth retardation, and a high incidence of abnormalities of the female and male reproductive organs including cryptorchidism. This may thus serve as a model to dissect the mechanisms involved in the development of the reproductive tract including testicular descent. Gene-targeted mice also display a reduction in the thickness of the zona reticularis of the adrenal gland and transient aberrations of the T and B cell compartments of primary lymphoid organs. These data show that this novel DNA-binding protein, Desrt, has a nonredundant function during growth and in the development of the reproductive system.

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