Molecular Analyses of Human Induced Pluripotent Stem Cells and Embryonic Stem Cells
Recent work from our group and others has argued that human induced pluripotent stem cells (hiPSCs) generated by the introduction of four viruses bearing reprogramming factors differ from human embryonic stem cells (hESCs) at the level of gene expression (Chin et al., 2009). Many of the differences...
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Published in | Cell stem cell Vol. 7; no. 2; pp. 263 - 269 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge, MA
Elsevier Inc
06.08.2010
Cell Press |
Subjects | |
Online Access | Get full text |
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Summary: | Recent work from our group and others has argued that human induced pluripotent stem cells (hiPSCs) generated by the introduction of four viruses bearing reprogramming factors differ from human embryonic stem cells (hESCs) at the level of gene expression (Chin et al., 2009). Many of the differences seen were common across independent labs and, at least to some extent, are thought to be a result of residual expression of donor cell-specific genes (Chin et al., 2009; Ghosh et al., 2010; Marchetto et al., 2009). Two new reports reanalyze similar expression data sets as those used in Chin et al. (2009) and come to different conclusions (Newman and Cooper, 2010; Guenther et al., 2010). We compare various approaches to perform gene expression meta-analysis that all support our original conclusions and present new data to demonstrate that polycistronic delivery of the reprogramming factors and extended culture brings hiPSCs transcriptionally closer to hESCs.
► Original study controlled for lab-specific variation ► Reanalysis of gene expression data sets confirms ESC versus iPSC differences ► Data from additional lines confirm previous findings ► Call for community discussion of “best practice” for expression data meta-analysis |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Commentary-1 ObjectType-Feature-1 |
ISSN: | 1934-5909 1875-9777 |
DOI: | 10.1016/j.stem.2010.06.019 |