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PMID: 20887957 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Identification and classification of chromosomal aberrations in human induced pluripotent stem cells.

Cell stem cell ·Vol. 7 ·No. 4 ·2010-10-08 ·Pages 521-31

Mayshar Y, Ben-David U, Lavon N, Biancotti JC, Yakir B, Clark AT, Plath K, Lowry WE, Benvenisty N

Abstract

Because of their somatic cell origin, human induced pluripotent stem cells (HiPSCs) are assumed to carry a normal diploid genome, and adaptive chromosomal aberrations have not been fully evaluated. Here, we analyzed the chromosomal integrity of 66 HiPSC and 38 human embryonic stem cell (HESC) samples from 18 different studies by global gene expression meta-analysis. We report identification of a substantial number of cell lines carrying full and partial chromosomal aberrations, half of which were validated at the DNA level. Several aberrations resulted from culture adaptation, and others are suspected to originate from the parent somatic cell. Our classification revealed a third type of aneuploidy already evident in early passage HiPSCs, suggesting considerable selective pressure during the reprogramming process. The analysis indicated high incidence of chromosome 12 duplications, resulting in significant enrichment for cell cycle-related genes. Such aneuploidy may limit the differentiation capacity and increase the tumorigenicity of HiPSCs.

MeSH Terms
Aneuploidy Chromosome Aberrations/classification Gene Expression Profiling Humans Induced Pluripotent Stem Cells
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Mayshar Yoav
Department of Genetics, Silberman Institute of Life Sciences, The Hebrew University, Jerusalem 91904, Israel.
Ben-David Uri
Lavon Neta
Biancotti Juan-Carlos
Yakir Benjamin
Clark Amander T
Plath Kathrin
Lowry William E
Benvenisty Nissim
Article Info
Journal
Cell stem cell
Abbr.
Cell Stem Cell
ISSN
1875-9777
Published
2010-10-08
Pages
521-31
Language
English
Region
United States
NLM ID
101311472
Subset
IM
Grants
NIGMS NIH HHS · P01 GM099134 · United States
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