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Complement in urochordates: cloning and characterization of two C3-like genes in the ascidian Ciona intestinalis

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Abstract

The recent identification of complement components in deuterostome invertebrates has indicated the presence of a complement system operating via an alternative pathway in echinoderms and tunicates and via a MBL-mediated pathway thus far identified only in tunicates. Here, we report the isolation of two C3-like genes, CiC3-1 and CiC3-2, from blood cell total RNA of the ascidian Ciona intestinalis. The deduced amino acid sequences of both Ciona C3-like proteins exhibit a canonical processing site for α and β chains, a thioester site with an associated catalytic histidine and a convertase cleavage site, thus showing an overall similarity to the other C3 molecules already characterized. Southern blotting analysis indicated that each gene is present as a single copy per haploid genome. In situ hybridization experiments showed that both CiC3-1 and CiC3-2 are expressed in one type of blood cell, the compartment cells. Two polyclonal antibodies, raised against two deduced peptide sequences in the α chain of CiC3-1 and CiC3-2, allowed the identification by Western blot of a single band in the blood serum, of about M r 150,000. A phylogenetic tree, based on the alignment of CiC3-1 and CiC3-2 with molecules of the α2-macroglobulin superfamily, indicated that the Ciona C3s form a cluster with Halocynthia roretzi C3. The phylogenetic analysis also suggested that the duplication event from which the CiC3-1 and CiC3-2 genes originated occurred in the urochordate lineage after the separation of the Halocynthia and Ciona ancestor.

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Marino, R., Kimura, Y., De Santis, R. et al. Complement in urochordates: cloning and characterization of two C3-like genes in the ascidian Ciona intestinalis . Immunogenetics 53, 1055–1064 (2002). https://doi.org/10.1007/s00251-001-0421-9

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  • DOI: https://doi.org/10.1007/s00251-001-0421-9

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