Back to Search Start Over

Bovine β-defensin gene family: opportunities to improve animal health?

Authors :
Meade, K. G.
Cormican, P.
Narciandi, F.
Lloyd, A.
O'Farrelly, C.
Source :
Physiological Genomics; 1/1/2014, Vol. 46 Issue 1, p17-28, 12p
Publication Year :
2014

Abstract

Recent analysis of the bovine genome revealed an expanded suite of defensin genes that encode what are referred to as antimicrobial or host defense peptides (HDPs). Whereas primate genomes also encode α- and θ-defensins, the bovine genome contains only the β-defensin subfamily of HDPs. β-Defensins perform diverse functions that are critical to protection against pathogens but also in regulation of the immune response and reproduction. As the most comprehensively studied subclass of HDPs, β-defensins possess the widest taxonomic distribution, found in invertebrates as well as plants, indicating an ancient point of origin. Cross-species comparison of the genomic arrangement of β-defensin gene repertoire revealed them to vary in number among species presumably due to differences in pathogenic selective pressures but also genetic drift. β-Defensin genes exist in a single cluster in birds, but four gene clusters exist in dog, rat, mouse, and cow. In humans and chimpanzees, one of these clusters is split in two as a result of a primate-specific pericentric inversion producing five gene clusters. A cluster of β-defensin genes on bovine chromosome 13 has been recently characterized, and full genome sequencing has identified extensive gene copy number variation on chromosome 27. As a result, cattle have the most diverse repertoire of β-defensin genes so far identified, where four clusters contain at least 57 genes. This expansion of β-defensin HDPs may hold significant potential for combating infectious diseases and provides opportunities to harness their immunological and reproductive functions in commercial cattle populations. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10948341
Volume :
46
Issue :
1
Database :
Complementary Index
Journal :
Physiological Genomics
Publication Type :
Academic Journal
Accession number :
103743276
Full Text :
https://doi.org/10.1152/physiolgenomics.00085.2013