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      DC-SIGN; a related gene, DC-SIGNR; and CD23 form a cluster on 19p13.

      The Journal of Immunology Author Choice
      Amino Acid Sequence, Cell Adhesion Molecules, Cell Line, Chromosome Mapping, Chromosomes, Human, Pair 19, immunology, Cloning, Molecular, DNA, Complementary, chemistry, isolation & purification, Dendritic Cells, metabolism, Exons, Gene Expression, Genetic Linkage, Humans, Introns, Lectins, biosynthesis, genetics, Lectins, C-Type, Molecular Sequence Data, Multigene Family, Organ Specificity, Receptors, Cell Surface, Receptors, IgE, Reverse Transcriptase Polymerase Chain Reaction

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          Abstract

          DC-SIGN is a C-type lectin, expressed on a dendritic cell subset. It is able to bind ICAM3 and HIV gp120 in a calcium-dependent manner. Here we report the genomic organization of DC-SIGN and map it to chromosome 19p13 adjacent to the C-type lectin CD23 (FcepsilonRII). We also report a novel, closely linked gene, DC-SIGNR, which shows 73% identity to DC-SIGN at the nucleic acid level and a similar genomic organization. Proteins encoded by both genes have tracts of repeats of 23 aa, predicted to form a coiled coil neck region. They also possess motifs that are known to bind mannose in a calcium-dependent fashion. We show concomitant expression of the two genes in endometrium, placenta, and stimulated KG1 cells (phenotypically similar to monocyte-derived dendritic cells). The existence of a DC-SIGN-related gene calls for reinterpretation of the HIV data to consider possible DC-SIGN/DC-SIGNR hetero-oligomerization.

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