Evolution of the interferon alpha gene family in eutherian mammals

Woelk, C.H., Frost, S.D.W., Richman, D.D., Higley, P.E. and Kosakovsky Pond, S.L. (2007) Evolution of the interferon alpha gene family in eutherian mammals Gene, 397, (1-2), pp. 38-50. (doi:10.1016/j.gene.2007.03.018).


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Interferon alpha (IFNA) genes code for proteins with important signaling roles during the innate immune response. Phylogenetically, IFNA family members in eutherians (placental mammals) cluster together in a species-specific manner except for closely related species (i.e. Homo sapiens and Pan troglodytes) where gene-specific clustering is evident. Previous research has been unable to clarify whether gene conversion or recent gene duplication accounts for gene-specific clustering, partly because the similarity of members of the IFNA family within species has made it historically difficult to identify the exact composition of IFNA gene families. IFNA gene families were fully characterized in recently available genomes from Canis familiaris, Macaca mulatta, P. troglodytes and Rattus norvegicus, and combined with previously characterized IFNA gene families from H. sapiens and Mus musculus, for the analysis of both whole and partial gene conversion events using a variety of statistical methods. Gene conversion was inferred in every eutherian species analyzed and comparison of the IFNA gene family locus between primate species revealed independent gene duplication in M. mulatta. Thus, both gene conversion and gene duplication have shaped the evolution of the IFNA gene family in eutherian species. Scenarios may be envisaged whereby the increased production of a specific IFN-? protein would be beneficial against a particular pathogenic infection. Gene conversion, similar to duplication, provides a mechanism by which the protein product of a specific IFNA gene can be increased.

Item Type: Article
Digital Object Identifier (DOI): doi:10.1016/j.gene.2007.03.018
ISSNs: 0378-1119 (print)
Keywords: interferon alpha, gene conversion, gene duplication, innate immunity
Organisations: Clinical & Experimental Sciences
ePrint ID: 352764
Date :
Date Event
August 2007Published
Date Deposited: 04 Jun 2013 15:04
Last Modified: 17 Apr 2017 15:30
Further Information:Google Scholar
URI: http://eprints.soton.ac.uk/id/eprint/352764

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