Characterization of the bovine type I IFN locus: rearrangements, expansions, and novel subfamilies

<p>Abstract</p> <p>Background</p> <p>The Type I interferons (IFN) have major roles in the innate immune response to viruses, a function that is believed to have led to expansion in the number and complexity of their genes, although these genes have remained confined to...

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Main Authors: Walker Angela M, Roberts R Michael
Format: Article
Language:English
Published: BMC 2009-04-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/10/187
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spelling doaj-46082d272e0849fb9be6707ee9c439b92020-11-24T21:44:40ZengBMCBMC Genomics1471-21642009-04-0110118710.1186/1471-2164-10-187Characterization of the bovine type I IFN locus: rearrangements, expansions, and novel subfamiliesWalker Angela MRoberts R Michael<p>Abstract</p> <p>Background</p> <p>The Type I interferons (IFN) have major roles in the innate immune response to viruses, a function that is believed to have led to expansion in the number and complexity of their genes, although these genes have remained confined to single chromosomal region in all mammals so far examined. <it>IFNB </it>and <it>IFNE </it>define the limits of the locus, with all other Type I IFN genes except <it>IFNK </it>distributed between these boundaries, strongly suggesting that the locus has broadened as IFN genes duplicated and then evolved into a series of distinct families.</p> <p>Results</p> <p>The Type I IFN locus in <it>Bos taurus </it>has undergone significant rearrangement and expansion compared to mouse and human, however, with the constituent genes separated into two sub-loci separated by >700 kb. The <it>IFNW </it>family is greatly expanded, comprising 24 potentially functional genes and at least 8 pseudogenes. The <it>IFNB </it>(n = 6), represented in human and mouse by one copy, are also present as multiple copies in <it>Bos taurus</it>. The <it>IFNT</it>, which encode a non-virally inducible, ruminant-specific IFN secreted by the pre-implantation conceptus, are represented by three genes and two pseudogenes. The latter have sequences intermediate between <it>IFNT </it>and <it>IFNW</it>. A new Type I IFN family (<it>IFNX</it>) of four members, one of which is a pseudogene, appears to have diverged from the <it>IFNA </it>lineage at least 83 million years ago, but is absent in all other sequenced genomes with the possible exception of the horse, a non-ruminant herbivore.</p> <p>Conclusion</p> <p>In summary, we have provided the first comprehensive annotation of the Type I IFN locus in <it>Bos taurus</it>, thereby providing an insight into the functional evolution of the Type I IFN in ruminants. The diversity and global spread of the ruminant species may have required an expansion of the Type I IFN locus and its constituent genes to provide broad anti-viral protection required for foraging and foregut fermentation.</p> http://www.biomedcentral.com/1471-2164/10/187
collection DOAJ
language English
format Article
sources DOAJ
author Walker Angela M
Roberts R Michael
spellingShingle Walker Angela M
Roberts R Michael
Characterization of the bovine type I IFN locus: rearrangements, expansions, and novel subfamilies
BMC Genomics
author_facet Walker Angela M
Roberts R Michael
author_sort Walker Angela M
title Characterization of the bovine type I IFN locus: rearrangements, expansions, and novel subfamilies
title_short Characterization of the bovine type I IFN locus: rearrangements, expansions, and novel subfamilies
title_full Characterization of the bovine type I IFN locus: rearrangements, expansions, and novel subfamilies
title_fullStr Characterization of the bovine type I IFN locus: rearrangements, expansions, and novel subfamilies
title_full_unstemmed Characterization of the bovine type I IFN locus: rearrangements, expansions, and novel subfamilies
title_sort characterization of the bovine type i ifn locus: rearrangements, expansions, and novel subfamilies
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2009-04-01
description <p>Abstract</p> <p>Background</p> <p>The Type I interferons (IFN) have major roles in the innate immune response to viruses, a function that is believed to have led to expansion in the number and complexity of their genes, although these genes have remained confined to single chromosomal region in all mammals so far examined. <it>IFNB </it>and <it>IFNE </it>define the limits of the locus, with all other Type I IFN genes except <it>IFNK </it>distributed between these boundaries, strongly suggesting that the locus has broadened as IFN genes duplicated and then evolved into a series of distinct families.</p> <p>Results</p> <p>The Type I IFN locus in <it>Bos taurus </it>has undergone significant rearrangement and expansion compared to mouse and human, however, with the constituent genes separated into two sub-loci separated by >700 kb. The <it>IFNW </it>family is greatly expanded, comprising 24 potentially functional genes and at least 8 pseudogenes. The <it>IFNB </it>(n = 6), represented in human and mouse by one copy, are also present as multiple copies in <it>Bos taurus</it>. The <it>IFNT</it>, which encode a non-virally inducible, ruminant-specific IFN secreted by the pre-implantation conceptus, are represented by three genes and two pseudogenes. The latter have sequences intermediate between <it>IFNT </it>and <it>IFNW</it>. A new Type I IFN family (<it>IFNX</it>) of four members, one of which is a pseudogene, appears to have diverged from the <it>IFNA </it>lineage at least 83 million years ago, but is absent in all other sequenced genomes with the possible exception of the horse, a non-ruminant herbivore.</p> <p>Conclusion</p> <p>In summary, we have provided the first comprehensive annotation of the Type I IFN locus in <it>Bos taurus</it>, thereby providing an insight into the functional evolution of the Type I IFN in ruminants. The diversity and global spread of the ruminant species may have required an expansion of the Type I IFN locus and its constituent genes to provide broad anti-viral protection required for foraging and foregut fermentation.</p>
url http://www.biomedcentral.com/1471-2164/10/187
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