Inducing Somatic Pkd1 Mutations in Vivo in a Mouse Model of Autosomal-Dominant Polycystic Kidney Disease

Abstract

Autosomal Dominant Polycystic Kidney Disease (ADPKD) is one of the worlds most common life-threatening genetic diseases. Over 95 of diagnosed cases of ADPKD are caused by mutations in PKD1 or PKD2 genes. The overall goal of this project is to identify, at the single cell level, the mechanisms that drive the progression of a homozygous Pkd2 null renal cell towards a pathogenic clonal cyst in a mouse model of ADPKD. We have established two genetic models to induce mutations: one during embryogenesis (Six2-cre) and one in the adult(Villin-cre). The embryonic model has generated clones of wild type and mutant cells that persist in the adult. The adult model has failed to induce sufficient recombination. In this report we summarize the results obtained with the embryonic model while proposing an alternative approach to increase recombination efficiency.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2016
Accession Number
AD1046750

Entities

People

  • Cristina Cebrian-ligero

Organizations

  • Board of Regents of the University of Michigan

Tags

DTIC Thesaurus Topics

  • Biomedical Research
  • Cell Polarity
  • Cells
  • Chromosomes
  • Demographic Cohorts
  • Diseases And Disorders
  • Electronic Mail
  • Frequency
  • Genes
  • Genetic Diseases
  • Genetic Phenomena
  • Genetics
  • Kidney Diseases
  • Medical Personnel
  • Mutations
  • Professional Development
  • Students

Fields of Study

  • Biology

Readers

  • Molecular Biology and Genetics
  • Molecular and Cellular Biochemistry
  • Oncology

Technology Areas

  • Biotechnology