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Stem-cell genomics

Jonathan B Weitzman

Author Affiliations

Genome Biology 2001, 2:spotlight-20010706-01  doi:10.1186/gb-spotlight-20010706-01


The electronic version of this article is the complete one and can be found online at:


Published:6 July 2001

© 2001 BioMed Central Ltd

Research news

The surprising plasticity and trans-differentiation of transplanted stem-cells suggest that there may be a set of universal stem-cell genes that govern the undifferentiated proliferative state. In the July 3 Proceedings of the National Academy of Sciences, Terskikh et al. report attempts to define a common stem-cell gene profile by comparing hematopoietic and neural stem-cells (Proc Natl Acad Sci USA 2001, 98:7934-7939). They isolated hematopoietic stem cells (HSC) from mouse bone marrow and created a subtracted cDNA library enriched in HSC genes. High-throughput sequencing identified 223 sequences representing known (40%) and novel genes. There were similarities and differences between these adult HSC genes and those characterized in fetal HSC. The HSC enrichment was demonstrated by PCR, northern and in situ hybridization experiments. The genes encode cell-surface proteins (notably two novel seven-transmembrane receptors), nuclear proteins and signalling molecules. Terskikh et al. compared their results with analysis of neural stem cells and performed microarray analysis to define common stem-cell genes. Some of the HSC-enriched genes were expressed in the germinal zones of the brain, which contain neural progenitor cells. The authors suggest that identifying overlapping stem-cell gene profiles may indicate genes that regulate the common feature of stem cells, namely their capacity for self-renewal.

References

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    PubMed Abstract | Publisher Full Text OpenURL

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    PubMed Abstract | Publisher Full Text OpenURL