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Nucleic Acids Research, Vol 27, Issue 17 e17-e17, Copyright © 1999 by Oxford University Press

ARTICLES

Serial analysis of gene expression: rapid RT-PCR analysis of unknown SAGE tags

A van den Berg, J van der Leij and S Poppema
Department of Pathology and Laboratory Medicine, University Hospital Groningen, PO Box 30.001, 9700 Groningen, The Netherlands.

In a pilot study on SAGE on Reed-Sternberg cells we have sequenced 1055 tags representing 701 genes. Screening of the GenBank database resulted in the identification of a corresponding gene or EST for 490 of them. For 211 of the tags no homology could be detected. A major problem of the serial analysis of gene expression (SAGE) approach is how to further analyse the unknown tags. We have developed an RT-PCR-based method, rapid analysis of unknown SAGE tags (RAST-PCR), to analyse the expression of the corresponding genes. This approach can be used as a screening method to investigate whether or not the gene is differentially expressed between several cell types of interest.
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