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. 2013 Mar 8;2(1):39–51.

Table 2.

Genomic alterations of induced pluripotent stem (iPS) cells

Cell type Factors used for repro-gramming No of aberrant/analysed clones Karyotype Literature
miPS cell lines 4 factors including c-Myc 6 of 9 cell lines Trisomy or Robertsonian translocation of chromosome 14, trisomy 8 Chen Q et al, Chromosome Res (2011) [29]
miPS cell lines Various conditions 27 of 127 cell lines with gene expression profiles obtained from the GEO database* Trisomy 8, trisomy 11/gains of 11D-11E, deletions of 14C-14E Ben-David U & Benvenisty N, Stem Cells (2012) [18]
hiPSC Non-Silencing of 4 factors 1 of 4 clones using karyotyping and mFISH Translocation between chromosome 1 and 17, gain of 1q, trisomy 5 Ramos-Mejia V et al, Cell Res (2010) [26]
hiPSC Cell lines from different institutions 13 of 66 cell lines with gene expression profiles obtained from the GEO database* Trisomy 1, 9, 12 and 17, gain of 12p and 17q, Loss of 15q Mayshar Y et al, Cell Stem Cell (2010) [23]
hiPS cell llines No influence of reprogramming factors 22 hiPS cell lines analysed with SNP arrays Median number of of copy number variations (CNV) 109; higher number in early than in late passages Hussein SM et al, Nature (2011) [13]
hiPSC Cell lines from different institutions 3 of 11 cell lines analysed with karyotyping and SNP arrays Extra copies of chromosome 12, inversion of chromosome 5 The International Stem Cell Initiative, Nat Biotechnol (2011) [14]
hiPS Different time points during cultivation and differentiation 37 cell lines analysed with high-resolution SNP arrays Deletions of regions containing tumor suppressor genes, duplications of regions containing oncogenes Laurent LC et al, Cell Stem Cell 2011) [15]
hiPSC Reprogramming by 4 of 8, 2 of 6, 3 of 4 clones, resp, using array containing probes for chr. 5-13 and parts of chr. 4 and 14 Deletion of chromosome 9, 13, 14, duplication of chromosome 13, gain of chromosome 8, amplification of chromosome 7 Pasi CE et al, Cell Death Diff (2011) [28]
- c-MYC
- 3 factors
- 4 factors
hiPSC Prolonged culture 1 of 2 cell lines analysed by G-banding, aCGH, FISH ish amp(1)(q21qter) Dekel-Naftali et al, Eur J Hum Genet (2012) [21]
*

chromosome aberrations were detected by a methodology based on gene expression profiling (Ben-David et al., Cell Stem Cell 2011 [59]).