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Profiling of differentially expressed genes in human stem cells by cDNA microarray

Authors
Kim, Chul GeunLee, Jong JooJung, Dae YoungJeon, JinseonHeo, Hyen SeokKang, Ho ChulShin, June HoCho, Yoon ShinChat, Kyung JoonKim, Chan GilDo, Byung-RokKim, Kyung SukKims, Hyun-Soo
Issue Date
Jun-2006
Publisher
KOREAN SOC MOLECULAR & CELLULAR BIOLOGY
Keywords
cDNA microarray; expression profiling; human CD34(+); hematopoietic stem/progenitor cells; human CD133(+) hematopoietic; stem/progenitor cells; human embryonic stem cells; human mesenchymal stem cells; stem cell signature
Citation
MOLECULES AND CELLS, v.21, no.3, pp.343 - 355
Indexed
SCIE
SCOPUS
KCI
Journal Title
MOLECULES AND CELLS
Volume
21
Number
3
Start Page
343
End Page
355
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/181400
ISSN
1016-8478
Abstract
Stem cells are unique cell populations with the ability to undergo both self-renewal and differentiation, although a wide variety of adult stem cells as well as embryonic stem cells have been identified and stem cell plasticity has recently been reported. To identify genes implicated in the control of the stem cell state as well as the characteristics of each stem cell line, we analyzed the expression profiles of genes in human embryonic, hematopoietic (CD34(+) and CD133(+)), and mesenchymal stem cells using cDNA microarrays, and identified genes that were differentially expressed in specific stem cell populations. In particular we were able to identify potential hESC signature-like genes that encode transcription factors (TFAP2C and MYCN), an RNA binding protein (IMP-3), and a functionally uncharacterized protein (MAGEA4). The overlapping sets of 22 up-regulated and 141 downregulated genes identified in this study of three human stem cell types may also provide insight into the developmental mechanisms common to all human stem cells. Furthermore, our comprehensive analyses of gene expression profiles in various adult stem cells may help to identify the genetic pathways involved in self-renewal as well as in multi-lineage specific differentiation.
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