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Stem Cell Reviews and Reports

, Volume 9, Issue 4, pp 523–530 | Cite as

Use of UTF1 Genetic Control Elements as iPSC Reporter

  • Amir Morshedi
  • Monireh Soroush Noghabi
  • Peter DrögeEmail author
Article

Abstract

The reprogramming of adult somatic cells into an embryonic stem cell (ESC) state by various means has opened a new chapter in basic and applied life science. While this technology will create great opportunities for regenerative medicine, the more immediate impact is likely to be found in human disease modeling and drug testing/development. An important aspect in the latter contexts is the ability to reliably monitor the pluripotent stem cell state, in particular with respect to human cell reprogramming using patient-specific somatic cells and high-throughput screens. Undifferentiated transcription factor 1 (UTF1) belongs to the core transcriptional network characterizing pluripotency. UTF1 is involved in ESC-specific chromatin organization, and its expression pattern during cell reprogramming and subsequent differentiation appears to be tightly connected with the pluripotent stem cell state. Here, we capitalized on these features and generated a reliable reporter system that was used to monitor induced pluripotent stem cell (iPSC) formation and subsequent differentiation. Our reporter cassette comprises less than 2.3 kb and remains functional during many cell passages after genomic integration. The fact that the human UTF1 genetic control elements work in a mouse background and the demonstrated functionality of the reporter in an epigenetic state further qualifies this system as a versatile new tool for iPSC research.

Keywords

Induced pluripotent stem cells Undifferentiated transcription factor 1 Pluripotency reporter Differentiation Reporter gene silencing 

Notes

Acknowledgements

Special thanks go to Drs. K. Karjalainen and K. Pfannkuche for retroviral 4F expression vectors and a modified cardiomyocyte differentiation protocol, respectively. We also thank Dr. L.-F. Zhang for the provision of mESCs. This work was funded by the National Medical Research Council, Singapore (NMRC1114/2007), and SINGA (A*STAR) and NTU graduate scholarships.

Author Contributions

A.M.: collection of data, conception and design, analysis and interpretation, manuscript writing; M.S.N.: cell culture; manuscript writing; P.D.: conception, design, analysis and interpretation, manuscript writing.

Conflict of Interest

The authors indicate no potential conflicts of interest.

Supplementary material

12015_2011_9342_MOESM1_ESM.xlsx (21 kb)
Suppl. Table 1 (XLSX 20 kb)
12015_2011_9342_MOESM2_ESM.xlsx (70 kb)
Suppl. Table 2 (XLSX 70 kb)

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Copyright information

© Springer Science+Business Media, LLC 2011

Authors and Affiliations

  • Amir Morshedi
    • 1
  • Monireh Soroush Noghabi
    • 2
  • Peter Dröge
    • 1
    Email author
  1. 1.School of Biological SciencesNanyang Technological UniversitySingaporeSingapore
  2. 2.Stem Cell and Developmental Biology, Genome Institute of SingaporeSingaporeSingapore

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