2010
High-resolution DNA analysis of human embryonic stem cell lines reveals culture-induced copy number changes and loss of heterozygosity
NARVA, Elisa; Reija AUTIO; Nelly RAHKONEN; Lingjia KONG; Neil HARRISON et al.Základní údaje
Originální název
High-resolution DNA analysis of human embryonic stem cell lines reveals culture-induced copy number changes and loss of heterozygosity
Autoři
NARVA, Elisa; Reija AUTIO; Nelly RAHKONEN; Lingjia KONG; Neil HARRISON; Danny KITSBERG; Lodovica BORGHESE; Joseph ITSKOVITZ-ELDOR; Omid RASOOL; Petr DVOŘÁK; Outi HOVATTA; Timo OTONSKI; Timo TUURI; Wei CUI; Oliver BRUSTLE; Duncan BAKER; Edna MALTBY; Harry D. MOORE; Nissim BEVENISTY; Peter W. ANDREWS; Olli YLI-HARJA a Riita LAHESMAA
Vydání
Nature Biotechnology, 2010, 1087-0156
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
Genetika a molekulární biologie
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 31.090
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/10:00043710
Organizační jednotka
Lékařská fakulta
UT WoS
Klíčová slova anglicky
COMPARATIVE GENOMIC HYBRIDIZATION; ES CELLS; INSTABILITY; EXPRESSION; CANCER; CHROMOSOME-16; CARCINOMA; GENES
Změněno: 18. 1. 2011 14:52, prof. Ing. Petr Dvořák, CSc.
Anotace
V originále
Prolonged culture of human embryonic stem cells (hESCs) can lead to adaptation and the acquisition of chromosomal abnormalities, underscoring the need for rigorous genetic analysis of these cells. Here we report the highest-resolution study of hESCs to date using an Affymetrix SNP 6.0 array containing 906,600 probes for single nucleotide polymorphisms (SNPs) and 946,000 probes for copy number variations (CNVs). Analysis of 17 different hESC lines maintained in different laboratories identified 843 CNVs of 50 kb-3 Mb in size. We identified, on average, 24% of the loss of heterozygosity (LOH) sites and 66% of the CNVs changed in culture between early and late passages of the same lines. Thirty percent of the genes detected within CNV sites had altered expression compared to samples with normal copy number states, of which >44% were functionally linked to cancer. Furthermore, LOH of the q arm of chromosome 16, which has not been observed previously in hESCs, was detected.
Návaznosti
| LC06077, projekt VaV |
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| MSM0021622430, záměr |
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