An atlas of human gene expression from massively parallel signature sequencing (MPSS)

  1. C. Victor Jongeneel1,6,
  2. Mauro Delorenzi2,
  3. Christian Iseli1,
  4. Daixing Zhou4,
  5. Christian D. Haudenschild4,
  6. Irina Khrebtukova4,
  7. Dmitry Kuznetsov1,
  8. Brian J. Stevenson1,
  9. Robert L. Strausberg5,
  10. Andrew J.G. Simpson3, and
  11. Thomas J. Vasicek4
  1. 1 Office of Information Technology, Ludwig Institute for Cancer Research, and Swiss Institute of Bioinformatics, 1015 Lausanne, Switzerland
  2. 2 National Center for Competence in Research in Molecular Oncology, Swiss Institute for Experimental Cancer Research (ISREC) and Swiss Institute of Bioinformatics, 1066 Epalinges, Switzerland
  3. 3 Ludwig Institute for Cancer Research, New York, New York 10012, USA
  4. 4 Solexa, Inc., Hayward, California 94545, USA
  5. 5 The J. Craig Venter Institute, Rockville, Maryland 20850, USA

Abstract

We have used massively parallel signature sequencing (MPSS) to sample the transcriptomes of 32 normal human tissues to an unprecedented depth, thus documenting the patterns of expression of almost 20,000 genes with high sensitivity and specificity. The data confirm the widely held belief that differences in gene expression between cell and tissue types are largely determined by transcripts derived from a limited number of tissue-specific genes, rather than by combinations of more promiscuously expressed genes. Expression of a little more than half of all known human genes seems to account for both the common requirements and the specific functions of the tissues sampled. A classification of tissues based on patterns of gene expression largely reproduces classifications based on anatomical and biochemical properties. The unbiased sampling of the human transcriptome achieved by MPSS supports the idea that most human genes have been mapped, if not functionally characterized. This data set should prove useful for the identification of tissue-specific genes, for the study of global changes induced by pathological conditions, and for the definition of a minimal set of genes necessary for basic cell maintenance. The data are available on the Web at http://mpss.licr.org and http://sgb.lynxgen.com.

Footnotes

  • [Supplemental material is available online at www.genome.org. The following individuals kindly provided reagents, samples, or unpublished information as indicated in the paper: A. Delaney.]

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.4041005.

  • 6 Corresponding author. E-mail Victor.Jongeneel{at}licr.org; fax 41-21-6924065.

    • Accepted April 21, 2005.
    • Received September 8, 2004.
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