[No authors listed]
The innate immune system includes antimicrobial peptides that protect multicellular organisms from a diverse spectrum of microorganisms. beta-Defensins comprise one important family of mammalian antimicrobial peptides. The annotation of the human genome fails to reveal the expected diversity, and a recent query of the draft sequence with the blast search engine found only one new beta-defensin gene (DEFB3). To define better the beta-defensin gene family, we adopted a genomics approach that uses hmmer, a computational search tool based on hidden Markov models, in combination with blast. This strategy identified 28 new human and 43 new mouse beta-defensin genes in five syntenic chromosomal regions. Within each syntenic cluster, the gene sequences and organization were similar, suggesting each cluster pair arose from a common ancestor and was retained because of conserved functions. Preliminary analysis indicates that at least 26 of the predicted genes are transcribed. These results demonstrate the value of a genomewide search strategy to identify genes with conserved structural motifs. Discovery of these genes represents a new starting point for exploring the role of beta-defensins in innate immunity.
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Defb7, Defb11, Defb15, Defb10, Defb36, DEFB118, DEFB104A, DEFB127, DEFB129, DEFB105A, DEFB106A, DEFB107A, DEFB108B, DEFB109P1, DEFB110, DEFB112, DEFB113, DEFB114, DEFB115, DEFB116, DEFB117, DEFB119, DEFB121, DEFB122, DEFB123, DEFB124, DEFB125, DEFB128, DEFB130, DEFB107B, DEFB104B, DEFB108P1, DEFB108P2, DEFB108P4, DEFB106B, DEFB105B, DEFB108P3, DEFB135, DEFB136, DEFB131, DEFB126
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