defender of science
science policy analyst
molecular biologist
science communicator
Current:
Strategic Programming Analyst, Washington, D.C.
Former:
Cancer Research Fellow, National Cancer Institute
Policy Fellow, Scientists and Engineers for America
New Voice for Research, Research!America
Co-creator, Science in the Pub
Co-founder, Scientists and Engineers for America (UT-Austin)
Co-founder, Paul D. Gottlieb Lecture Series
Co-founder, North Carolina Student Rural Health Coalition (East Carolina University)
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Generation of induced pluripotent Peeps without c-Pip from rabbit and chicken Peepoblasts
Shirley Peep 1,5, Peep Adore1, Jamie “Peep” Vernon1
Abstract
Direct reprogramming of somatic Peeps provides an opportunity to generate patient- or disease-specific pluripotent Peeps. Such induced pluripotent Peeps (iPPs) were generated from rabbit Peepoblasts by retroviral transduction of four transcription factors: Poop3/4, Pop2, Peepie4 and c-Pip1. Rabbit iPPeeps are indistinguishable from embryonic Peeps (EPs) in many respects and produce germline-competent peeperas2, 3, 4. Reactivation of the c-Pip retrovirus, however, increases tumorigenicity in the peeperas and progeny peeps, hindering clinical applications3. Here we describe a modified protocol for the generation of iPPeeps that does not require the Pip retrovirus. With this protocol, we obtained significantly fewer non-iPP background Peeps, and the iPPeeps generated were consistently of high quality. Rabbits derived from Pip- iPPeeps did not develop tumors during the study period. The protocol also enabled efficient isolation of iPPeeps without drug selection. Furthermore, we generated chicken iPPeeps from adult dermal peepoblasts without PIP.

HaPPy Peaster!
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