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Differentiating human embryonic stem cells express a unique housekeeping gene signature.

Synnergren, Jane, 1967 (författare)
Högskolan i Skövde,Institutionen för kommunikation och information
Giesler, Theresa L (författare)
GE Healthcare, Piscataway, NJ, United States
Adak, Sudeshna (författare)
GE John F. Welch Technology Centre Export Promotion Industrial Park, Bangalore, India
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Tandon, Reeti (författare)
GE John F. Welch Technology Centre Export Promotion Industrial Park, Bangalore, India
Noaksson, Karin (författare)
Cellartis AB, Göteborg, Sweden
Lindahl, Anders, 1954 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för klinisk kemi och transfusionsmedicin,Institute of Biomedicine, Department of Clinical Chemistry and Transfusion Medicine,Department of Clinical Chemistry/Transfusion Medicine, Sahlgrenska University Hospital, Göteborg, Sweden
Nilsson, Patric (författare)
Högskolan i Skövde,Institutionen för vård och natur
Nelson, Deirdre (författare)
GE Global Research Center, Niskayuna, NY, United States
Olsson, Björn (författare)
Högskolan i Skövde,Institutionen för kommunikation och information
Englund, Mikael C. O., 1971 (författare)
Cellartis AB, Göteborg, Sweden
Sartipy, Peter (författare)
Cellartis AB, Göteborg, Sweden / Cellartis AB, Arvid Wallgrens Backe 20, SE-41346 Göteborg, Sweden
Abbot, Stewart (författare)
GE Global Research Center, Niskayuna, NY, United States
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 (creator_code:org_t)
2007-02-01
2007
Engelska.
Ingår i: Stem cells (Dayton, Ohio). - : Oxford University Press (OUP). - 1066-5099 .- 1549-4918. ; 25:2, s. 473-80
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Housekeeping genes (HKGs) are involved in basic functions needed for the sustenance of the cell and are assumed to be constitutively expressed at a constant level. Based on these features, HKGs are frequently used for normalization of gene expression data. In the present study, we used the CodeLink Gene Expression Bioarray system to interrogate changes in gene expression occurring during differentiation of human ESCs (hESCs). Notably, in the three hESC lines used for the study, we observed that the RNA levels of 56 frequently used HKGs varied to a degree that rendered them inappropriate as reference genes. Therefore, we defined a novel set of HKGs specifically for hESCs. Here we present a comprehensive list of 292 genes that are stably expressed (coefficient of variation <20%) in differentiating hESCs. These genes were further grouped into high-, medium-, and low-expressed genes. The expression patterns of these novel HKGs show very little overlap with results obtained from somatic cells and tissues. We further explored the stability of this novel set of HKGs in independent, publicly available gene expression data from hESCs and observed substantial similarities with our results. Gene expression was confirmed by real-time quantitative polymerase chain reaction analysis. Taken together, these results suggest that differentiating hESCs have a unique HKG signature and underscore the necessity to validate the expression profiles of putative HKGs. In addition, this novel set of HKGs can preferentially be used as controls in gene expression analyses of differentiating hESCs.

Nyckelord

Animals
Biological Markers
metabolism
Cell Differentiation
genetics
Embryonic Stem Cells
cytology
metabolism
Gene Expression Profiling
Gene Expression Regulation
Genes
Essential
Humans
Mice
RNA
Messenger
genetics
metabolism
Reverse Transcriptase Polymerase Chain Reaction
Gene expression

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