Project: PRJNA539951
Here we analysed the transcriptomic response of human embryonic stem cell line H9 to sustained activation of the canonical Wnt pathway by eiother treating cells with CHIR99021 or recombinant Wnt3a or inducing the overexpression of constitutively active beta-catenin mutant Overall design: hESC cell line H9 was treated with 10 µM CHIR99021 or 240 ng/ml of rWnt3a. In parallel, H9 line with stable integration of doxycycline-regulatable deltaN90 mutant of beta-catenin was treated with 1 µg/ml of Doxycycline. Cells were collected at time points 0 hours (undifferentiated cells), 8 hours, 16 hours, 24 hours, 48 hours and 72 hours (additionally 96 and 120 hours for rWnt3a treatment) and subjected to total RNA sequencing using Illumina platform.
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