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Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage
Authors:International Stem Cell Initiative  Amps Katherine  Andrews Peter W  Anyfantis George  Armstrong Lyle  Avery Stuart  Baharvand Hossein  Baker Julie  Baker Duncan  Munoz Maria B  Beil Stephen  Benvenisty Nissim  Ben-Yosef Dalit  Biancotti Juan-Carlos  Bosman Alexis  Brena Romulo Martin  Brison Daniel  Caisander Gunilla  Camarasa María V  Chen Jieming  Chiao Eric  Choi Young Min  Choo Andre B H  Collins Daniel  Colman Alan  Crook Jeremy M  Daley George Q  Dalton Anne  De Sousa Paul A  Denning Chris  Downie Janet  Dvorak Petr  Montgomery Karen D  Feki Anis  Ford Angela  Fox Victoria  Fraga Ana M  Frumkin Tzvia  Ge Lin  Gokhale Paul J
Affiliation:Centre for Stem Cell Biology, Department of Biomedical Science, The University of Sheffield, Sheffield, UK.
Abstract:The International Stem Cell Initiative analyzed 125 human embryonic stem (ES) cell lines and 11 induced pluripotent stem (iPS) cell lines, from 38 laboratories worldwide, for genetic changes occurring during culture. Most lines were analyzed at an early and late passage. Single-nucleotide polymorphism (SNP) analysis revealed that they included representatives of most major ethnic groups. Most lines remained karyotypically normal, but there was a progressive tendency to acquire changes on prolonged culture, commonly affecting chromosomes 1, 12, 17 and 20. DNA methylation patterns changed haphazardly with no link to time in culture. Structural variants, determined from the SNP arrays, also appeared sporadically. No common variants related to culture were observed on chromosomes 1, 12 and 17, but a minimal amplicon in chromosome 20q11.21, including three genes expressed in human ES cells, ID1, BCL2L1 and HM13, occurred in >20% of the lines. Of these genes, BCL2L1 is a strong candidate for driving culture adaptation of ES cells.
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