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

被引:413
作者
Schutte, BC
Mitros, JP
Bartlettt, JA
Walters, JD
Jia, HP
Welsh, MJ
Casavant, TL
McCray, PB [1 ]
机构
[1] Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
[2] Univ Iowa, Genet PhD Program, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[4] Univ Iowa, Dept Physiol & Biophys, Iowa City, IA 52242 USA
[5] Univ Iowa, Howard Hughes Med Inst, Iowa City, IA 52242 USA
关键词
D O I
10.1073/pnas.042692699
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 (DEF83). To define better the G-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.
引用
收藏
页码:2129 / 2133
页数:5
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