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Protein O-mannosylation in the murine brain: Occurrence of Mono-O-Mannosyl glycans and identification of new substrates

2016, Bartels, Markus F., Winterhalter, Patrick R., Yu, Jin, Liu, Yan, Lommel, Mark, Möhrlen, Frank, Hu, Huaiyu, Feizi, Ten, Westerlind, Ulrika, Ruppert, Thomas, Strahl, Sabine

Protein O-mannosylation is a post-translational modification essential for correct development of mammals. In humans, deficient O-mannosylation results in severe congenital muscular dystrophies often associated with impaired brain and eye development. Although various O-mannosylated proteins have been identified in the recent years, the distribution of O-mannosyl glycans in the mammalian brain and target proteins are still not well defined. In the present study, rabbit monoclonal antibodies directed against the O-mannosylated peptide YAT(α1-Man)AV were generated. Detailed characterization of clone RKU-1-3-5 revealed that this monoclonal antibody recognizes O-linked mannose also in different peptide and protein contexts. Using this tool, we observed that mono-O-mannosyl glycans occur ubiquitously throughout the murine brain but are especially enriched at inhibitory GABAergic neurons and at the perineural nets. Using a mass spectrometry-based approach, we further identified glycoproteins from the murine brain that bear single O-mannose residues. Among the candidates identified are members of the cadherin and plexin superfamilies and the perineural net protein neurocan. In addition, we identified neurexin 3, a cell adhesion protein involved in synaptic plasticity, and inter-alpha-trypsin inhibitor 5, a protease inhibitor important in stabilizing the extracellular matrix, as new O-mannosylated glycoproteins.

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Discovery of 505-million-year old chitin in the basal demosponge Vauxia gracilenta

2013, Ehrlich, H., Rigby, J.K., Botting, J.P., Tsurkan, M.V., Werner, C., Schwille, P., Petrášek, Z., Pisera, A., Simon, P., Sivkov, V.N., Vyalikh, D.V., Molodtsov, S.L., Kurek, D., Kammer, M., Hunoldt, S., Born, R., Stawski, D., Steinhof, A., Bazhenov, V.V., Geisler, T.

Sponges are probably the earliest branching animals, and their fossil record dates back to the Precambrian. Identifying their skeletal structure and composition is thus a crucial step in improving our understanding of the early evolution of metazoans. Here, we present the discovery of 505-million-year-old chitin, found in exceptionally well preserved Vauxia gracilenta sponges from the Middle Cambrian Burgess Shale. Our new findings indicate that, given the right fossilization conditions, chitin is stable for much longer than previously suspected. The preservation of chitin in these fossils opens new avenues for research into other ancient fossil groups.