Unknown

Dataset Information

0

Novel codon-optimized mini-intronic plasmid for efficient, inexpensive, and xeno-free induction of pluripotency.


ABSTRACT: The development of human induced pluripotent stem cell (iPSC) technology has revolutionized the regenerative medicine field. This technology provides a powerful tool for disease modeling and drug screening approaches. To circumvent the risk of random integration into the host genome caused by retroviruses, non-integrating reprogramming methods have been developed. However, these techniques are relatively inefficient or expensive. The mini-intronic plasmid (MIP) is an alternative, robust transgene expression vector for reprogramming. Here we developed a single plasmid reprogramming system which carries codon-optimized (Co) sequences of the canonical reprogramming factors (Oct4, Klf4, Sox2, and c-Myc) and short hairpin RNA against p53 ("4-in-1 CoMiP"). We have derived human and mouse iPSC lines from fibroblasts by performing a single transfection. Either independently or together with an additional vector encoding for LIN28, NANOG, and GFP, we were also able to reprogram blood-derived peripheral blood mononuclear cells (PBMCs) into iPSCs. Taken together, the CoMiP system offers a new highly efficient, integration-free, easy to use, and inexpensive methodology for reprogramming. Furthermore, the CoMIP construct is color-labeled, free of any antibiotic selection cassettes, and independent of the requirement for expression of the Epstein-Barr Virus nuclear antigen (EBNA), making it particularly beneficial for future applications in regenerative medicine.

SUBMITTER: Diecke S 

PROVIDER: S-EPMC4308704 | biostudies-literature | 2015 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

Novel codon-optimized mini-intronic plasmid for efficient, inexpensive, and xeno-free induction of pluripotency.

Diecke Sebastian S   Lu Jiamiao J   Lee Jaecheol J   Termglinchan Vittavat V   Kooreman Nigel G NG   Burridge Paul W PW   Ebert Antje D AD   Churko Jared M JM   Sharma Arun A   Kay Mark A MA   Wu Joseph C JC  

Scientific reports 20150128


The development of human induced pluripotent stem cell (iPSC) technology has revolutionized the regenerative medicine field. This technology provides a powerful tool for disease modeling and drug screening approaches. To circumvent the risk of random integration into the host genome caused by retroviruses, non-integrating reprogramming methods have been developed. However, these techniques are relatively inefficient or expensive. The mini-intronic plasmid (MIP) is an alternative, robust transgen  ...[more]

Similar Datasets

| S-EPMC3666631 | biostudies-literature
| S-EPMC5087309 | biostudies-literature
| S-EPMC8402753 | biostudies-literature
| S-EPMC4265750 | biostudies-other
| S-EPMC8322621 | biostudies-literature
| S-EPMC7031065 | biostudies-literature
| S-EPMC5012651 | biostudies-literature
| S-EPMC4814334 | biostudies-literature
| S-EPMC7509596 | biostudies-literature
| S-EPMC5233437 | biostudies-literature