| Literature DB >> 27645998 |
Tomomi Izumikawa1, Katsufumi Dejima2, Yukiko Watamoto1, Kazuko H Nomura2, Nanako Kanaki2, Marika Rikitake2, Mai Tou2, Daisuke Murata2, Eri Yanagita2, Ai Kano2, Shohei Mitani3, Kazuya Nomura4, Hiroshi Kitagawa5.
Abstract
Chondroitin sulfate (CS)/chondroitin (Chn) chains are indispensable for embryonic cell division and cytokinesis in the early developmental stages in Caenorhabditis elegans and mice, whereas heparan sulfate (HS) is essential for axon guidance during nervous system development. These data indicate that the fundamental functions of CS and HS are conserved from worms to mammals and that the function of CS/Chn differs from that of HS. Although previous studies have shown that C. elegans produces HS and non-sulfated Chn, whether the organism produces CS remains unclear. Here, we demonstrate that C. elegans produces a small amount of 4-O-sulfated Chn and report the identification of C41C4.1, an orthologue of the human chondroitin 4-O-sulfotransferase gene. Loss of C41C4.1 in C. elegans resulted in a decline in 4-O-sulfation of CS and an increase in the number of sulfated units in HS. C41C4.1 deletion mutants exhibited reduced survival rates after synchronization with sodium hypochlorite. Collectively, these results show for the first time that CS glycans are present in C. elegans and that the Chn 4-O-sulfotransferase responsible for the sulfation plays an important role in protecting nematodes from oxidative stress.Entities:
Keywords: Caenorhabditis elegans (C. elegans); chondroitin sulfate; oxidative stress; proteoglycan; sulfotransferase
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Year: 2016 PMID: 27645998 PMCID: PMC5087745 DOI: 10.1074/jbc.M116.757328
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157