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Characterization of transgenic mice expressing cancer-associated variants of human NOTCH1

  1. Author:
    Berquam-Vrieze, K. E.
    Swing, D. A.
    Tessarollo, L.
    Dupuy, A. J.
  2. Author Address

    [Berquam-Vrieze, Katherine E.; Dupuy, Adam J.] Univ Iowa, Carver Coll Med, Dept Anat & Cell Biol, Iowa City, IA 52242 USA. [Swing, Deborah A.; Tessarollo, Lino] NCI, Mouse Canc Genet Program, Frederick, MD 21701 USA.;Dupuy, AJ (reprint author), Univ Iowa, Coll Med, Dept Anat & Cell Biol, Iowa City, IA 52242 USA;adam-dupuy@uiowa.edu
    1. Year: 2012
    2. Date: Feb
  1. Journal: Genesis
    1. 50
    2. 2
    3. Pages: 112-118
  2. Type of Article: Article
  3. ISSN: 1526-954X
  1. Abstract:

    The Notch1 receptor plays a critical role in cell fate decisions during development. Activation of Notch signaling has been implicated in several types of cancer, particularly T-cell acute lymphoblastic leukemia (T-ALL). Consequently, several transgenic mouse strains have been made to study the role of Notch1 in T-ALL. However, the existing Notch1 transgenic lines mimic a translocation event found in only similar to 1% of T-ALL cases. Here we describe three novel NOTCH1 transgenic mouse strains that have Cre-inducible expression of the entire human NOTCH1 locus, each possessing a common mutation found in T-ALL. Unlike existing Notch1 transgenic strains, these NOTCH1 transgenic strains express full-length receptors from anendogenous human promoter that should be susceptible to a number of Notch antagonists that have recently been developed. These strains will allow researchers to modulate Notch signaling to study bothnormal development and cancer biology. genesis 50:112118, 2012. (C) 2011 Wiley Periodicals, Inc.

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External Sources

  1. DOI: 10.1002/dvg.20798
  2. WOS: 000299835500004

Library Notes

  1. Fiscal Year: FY2011-2012
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