Differences in gene expression of human xylosyltransferases and determination of acceptor specificities for various proteoglycans

• Published in: Biochemical and biophysical research communications Vol. 391; no. 1; pp. 685 - 691
• Main Authors: Roch, Christina, Kuhn, Joachim, Kleesiek, Knut, Götting, Christian
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.2010
• Subjects: 60 APPLIED LIFE SCIENCES; Alpha-Globulins - chemistry; Alpha-Globulins - genetics; Amino Acid Motifs; AMINO ACID SEQUENCE; ANIMAL CELLS; BIOSYNTHESIS; CALVES; Cell Line; Gene Expression Regulation, Enzymologic; GENES; GLUTATHIONE; Glutathione Transferase - chemistry; Glutathione Transferase - genetics; Glycosaminoglycan; Glycosaminoglycans - chemistry; Glycosaminoglycans - genetics; HAMSTERS; Humans; IN VIVO; Isoenzymes - genetics; Kinetic analysis; MESSENGER-RNA; Molecular Sequence Data; MUTAGENESIS; MUTATIONS; OVARIES; Pentosyltransferases - chemistry; Pentosyltransferases - genetics; Proteoglycan; Proteoglycans - chemistry; Recombinant Fusion Proteins - chemistry; Recombinant Fusion Proteins - genetics; SPECIFICITY; UDP Xylose-Protein Xylosyltransferase; Xylose - chemistry; Xylosyltransferase; PBS; Proteoglycan; CI; Xylosyltransferase; GST; Kinetic analysis; CHO; GAG; XT-II; SD; XT-I; ND; FCS; PG; IPTG; Glycosaminoglycan; WT
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2009.11.121

The xylosyltransferase (XT) isoforms XT-I and XT-II initiate the posttranslational glycosaminoglycan (GAG) synthesis. Here, we determined the relative expression of both isoforms in 33 human cell lines. The majority of tested cell lines showed dominant XYLT2 gene expression, while only in 23132/87, JAR, NCI-H510A and THP-1 was the XT-I mRNA expression higher. Nearly equal expression levels were detected in six cell lines. Additionally, to shed light on putative differences in acceptor specificities the acceptor properties of potential acceptor sequences were determined. Peptides were expressed as glutathione-S-transferase fusion proteins containing putative or known GAG attachment sites of in vivo proteoglycans. Kinetic analysis showed that Km and Vmax values for XT-I mediated xylosylation were slightly higher than those for XT-II, and that XT-I showed a lesser stringency concerning the acceptor sequence. Mutagenesis of the bikunin peptide sequence in the G-S-G attachment site and flanking regions generated potential acceptor molecules. Here, mutations on the N-terminal side and the attachment site were found to be more susceptible to a loss of acceptor function than mutations in the C-terminus. Altogether the known consensus sequence a-a-a-a-G-S-G-a-a/G-a (‘a’ representing Asp or Glu) for XT-I mediated xylosylation could be approved and additionally extended to apply to XT-II as well.