Identification of a Small Molecule That Turns ON the Pluripotency Gene Circuitry in Human Fibroblasts
journal contributionposted on 19.12.2014, 00:00 by Ganesh N. Pandian, Shinsuke Sato, Chandran Anandhakumar, Junichi Taniguchi, Kazuhiro Takashima, Junetha Syed, Le Han, Abhijit Saha, Toshikazu Bando, Hiroki Nagase, Hiroshi Sugiyama
A nontransgenic approach to reprogram mouse somatic cells into induced pluripotent stem cells using only small molecules got achieved to propose a potential clinical-friendly cellular reprogramming strategy. Consequently, the screening and identification of small molecules capable of inducing pluripotency genes in human cells are increasingly a focus of research. Because cellular reprogramming is multifactorial in nature, there is a need for versatile small molecules capable of modulating the complicated gene networks associated with pluripotency. We have developed a targeting small molecule called SAHA-PIP comprising the histone deacetylase inhibitor SAHA and the sequence-specific DNA binding pyrrole-imidazole polyamides for modulating distinct gene networks. Here, we report the identification of a SAHA-PIP termed Ì that could trigger genome-wide epigenetic reprogramming and turn ON the typically conserved core pluripotency gene network. Through independent lines of evidence, we report for the first time a synthetic small molecule inducer that target and activate the OCT-3/4 regulated pluripotency genes in human dermal fibroblasts.