Abstract：
:Reprogramming somatic cells into induced pluripotent stem cells (iPSCs) has been suspected of causing de novo copy number variation. To explore this issue, here we perform a whole-genome and transcriptome analysis of 20 human iPSC lines derived from the primary skin fibroblasts of seven individuals using next-generation sequencing. We find that, on average, an iPSC line manifests two copy number variants (CNVs) not apparent in the fibroblasts from which the iPSC was derived. Using PCR and digital droplet PCR, we show that at least 50% of those CNVs are present as low-frequency somatic genomic variants in parental fibroblasts (that is, the fibroblasts from which each corresponding human iPSC line is derived), and are manifested in iPSC lines owing to their clonal origin. Hence, reprogramming does not necessarily lead to de novo CNVs in iPSCs, because most of the line-manifested CNVs reflect somatic mosaicism in the human skin. Moreover, our findings demonstrate that clonal expansion, and iPSC lines in particular, can be used as a discovery tool to reliably detect low-frequency CNVs in the tissue of origin. Overall, we estimate that approximately 30% of the fibroblast cells have somatic CNVs in their genomes, suggesting widespread somatic mosaicism in the human body. Our study paves the way to understanding the fundamental question of the extent to which cells of the human body normally acquire structural alterations in their DNA post-zygotically.
journal_name
Naturejournal_title
Natureauthors
Abyzov A,Mariani J,Palejev D,Zhang Y,Haney MS,Tomasini L,Ferrandino AF,Rosenberg Belmaker LA,Szekely A,Wilson M,Kocabas A,Calixto NE,Grigorenko EL,Huttner A,Chawarska K,Weissman S,Urban AE,Gerstein M,Vaccarino FMdoi
10.1038/nature11629subject
Has Abstractpub_date
2012-12-20 00:00:00pages
438-42issue
7429eissn
0028-0836issn
1476-4687pii
nature11629journal_volume
492pub_type
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