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Discovery of five conserved β-defensin gene clusters using a computational search strategy
Journal article   Open access   Peer reviewed

Discovery of five conserved β-defensin gene clusters using a computational search strategy

Brian C Schutte, Joseph P Mitros, Jennifer A Bartlett, Jesse D Walters, Hong Peng Jia, Michael J Welsh, Thomas L Casavant and Paul B McCray
Proceedings of the National Academy of Sciences - PNAS, Vol.99(4), pp.2129-2133
02/19/2002
DOI: 10.1073/pnas.042692699
PMCID: PMC122330
PMID: 11854508
url
https://doi.org/10.1073/pnas.042692699View
Published (Version of record) Open Access

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Abstract

The innate immune system includes antimicrobial peptides that protect multicellular organisms from a diverse spectrum of microorganisms. β-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 β-defensin gene ( DEFB3 ). To define better the β-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 β-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 β-defensins in innate immunity.
Biological Sciences

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