A general transcription co-factor, Smad3, potentiates master transcription factor mediated cell identity conversions [ChIP-seq]
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ABSTRACT: We have identified that expression of constitutive active Smad3 (Smad3CA) significantly enhanced reprogramming by Oct4, Sox2, Klf4, c-Myc. Smad3 is known to interact with several master transcription factors and boost their activity during development. Therefore, we hypothesized that Smad3CA is recruited to Oct4 binding sites during reprogramming. To test this hypothesis, we investigated genome-wide Smad3 binding sites in the presence and absence of reprogramming factor expression.
ORGANISM(S): Mus musculus
PROVIDER: GSE85177 | GEO | 2017/11/03
SECONDARY ACCESSION(S): PRJNA336441
REPOSITORIES: GEO
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