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Partial promoter substitutions generating transcriptional sentinels of diverse signaling pathways in embryonic stem cells and mice
Author(s) -
Palle Serup,
Carsten R. Gustavsen,
Tino Klein,
Leah A. Potter,
Robert Lin,
Nandita Mullapudi,
Ewa Wandzioch,
Angela Hines,
Ashley Davis,
Christine Bruun,
Nina Engberg,
Dorthe Roenn Petersen,
Janny M.L. Peterslund,
Raymond J. MacDonald,
Anne GrapinBotton,
Mark A. Magnuson,
Kenneth S. Zaret
Publication year - 2012
Publication title -
disease models and mechanisms
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.327
H-Index - 83
eISSN - 1754-8411
pISSN - 1754-8403
DOI - 10.1242/dmm.009696
Subject(s) - embryonic stem cell , biology , microbiology and biotechnology , stem cell , signal transduction , genetics , computational biology , gene
Extracellular signals in development, physiology, homeostasis and disease often act by regulating transcription. Herein we describe a general method and specific resources for determining where and when such signaling occurs in live animals and for systematically comparing the timing and extent of different signals in different cellular contexts. We used recombinase-mediated cassette exchange (RMCE) to test the effect of successively deleting conserved genomic regions of the ubiquitously active Rosa26 promoter and substituting the deleted regions for regulatory sequences that respond to diverse extracellular signals. We thereby created an allelic series of embryonic stem cells and mice, each containing a signal-responsive sentinel with different fluorescent reporters that respond with sensitivity and specificity to retinoic acids, bone morphogenic proteins, activin A, Wnts or Notch, and that can be adapted to any pathway that acts via DNA elements.

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