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Glycobiology Advance Access originally published online on October 19, 2005
Glycobiology 2006 16(2):117-131; doi:10.1093/glycob/cwj048
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© The Author 2005. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org

A focused microarray approach to functional glycomics: transcriptional regulation of the glycome

Elena M. Comelli1,3,4, Steven R. Head1,5, Tim Gilmartin5, Thomas Whisenant5, Stuart M. Haslam6, Simon J. North6, Nyet-Kui Wong6, Takashi Kudo7, Hisashi Narimatsu7, Jeffrey D. Esko8, Kurt Drickamer6, Anne Dell6 and James C. Paulson2,4

4 Department of Molecular Biology and Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA 92037; 5 DNA Microarray Core Facility, The Scripps Research Institute, La Jolla, CA 92037; 6 Imperial College London, South Kensington Campus, London SW7 2AZ, UK; 7 AIST, Tsukuba 305–8568, Japan; and 8 University of California San Diego, La Jolla, CA 92037


1 These authors contributed equally to this work.

2 To whom correspondence should be addressed; e-mail: jpaulson{at}scripps.edu

3 Present address: Nestlé Research Centre, Department of Nutrition and Health, Vers chez les Blanc, 1000 Lausanne 26, Switzerland

Received on July 15, 2005; revised on September 15, 2005; accepted on October 11, 2005

Glycosylation is the most common posttranslational modification of proteins, yet genes relevant to the synthesis of glycan structures and function are incompletely represented and poorly annotated on the commercially available arrays. To fill the need for expression analysis of such genes, we employed the Affymetrix technology to develop a focused and highly annotated glycogene-chip representing human and murine glycogenes, including glycosyltransferases, nucleotide sugar transporters, glycosidases, proteoglycans, and glycan-binding proteins. In this report, the array has been used to generate glycogene-expression profiles of nine murine tissues. Global analysis with a hierarchical clustering algorithm reveals that expression profiles in immune tissues (thymus [THY], spleen [SPL], lymph node, and bone marrow [BM]) are more closely related, relative to those of nonimmune tissues (kidney [KID], liver [LIV], brain [BRN], and testes [TES]). Of the biosynthetic enzymes, those responsible for synthesis of the core regions of N- and O-linked oligosaccharides are ubiquitously expressed, whereas glycosyltransferases that elaborate terminal structures are expressed in a highly tissue-specific manner, accounting for tissue and ultimately cell-type-specific glycosylation. Comparison of gene expression profiles with matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) profiling of N-linked oligosaccharides suggested that the {alpha}1-3 fucosyltransferase 9, Fut9, is the enzyme responsible for terminal fucosylation in KID and BRN, a finding validated by analysis of Fut9 knockout mice. Two families of glycan-binding proteins, C-type lectins and Siglecs, are predominately expressed in the immune tissues, consistent with their emerging functions in both innate and acquired immunity. The glycogene chip reported in this study is available to the scientific community through the Consortium for Functional Glycomics (CFG) (http://www.functionalglycomics.org).

Key words: Fut9 / glycomics / glycosyltransferase / lectin / microarray


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