Signatures of selection acting on the innate immunity gene Toll‐like receptor 2 (TLR2) during the evolutionary history of rodents

Patterns of selection acting on immune defence genes have recently been the focus of considerable interest. Yet, when it comes to vertebrates, studies have mainly focused on the acquired branch of the immune system. Consequently, the direction and strength of selection acting on genes of the vertebr...

Full description

Saved in:
Bibliographic Details
Published inJournal of evolutionary biology Vol. 24; no. 6; pp. 1232 - 1240
Main Authors TSCHIRREN, B., RÅBERG, L., WESTERDAHL, H.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.06.2011
Oxford University Press
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Patterns of selection acting on immune defence genes have recently been the focus of considerable interest. Yet, when it comes to vertebrates, studies have mainly focused on the acquired branch of the immune system. Consequently, the direction and strength of selection acting on genes of the vertebrate innate immune defence remain poorly understood. Here, we present a molecular analysis of selection on an important receptor of the innate immune system of vertebrates, the Toll‐like receptor 2 (TLR2), across 17 rodent species. Although purifying selection was the prevalent evolutionary force acting on most parts of the rodent TLR2, we found that codons in close proximity to pathogen‐binding and TLR2–TLR1 heterodimerization sites have been subject to positive selection. This indicates that parasite‐mediated selection is not restricted to acquired immune system genes like the major histocompatibility complex, but also affects innate defence genes. To obtain a comprehensive understanding of evolutionary processes in host–parasite systems, both innate and acquired immunity thus need to be considered.
Bibliography:SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 14
ObjectType-Article-1
ObjectType-Feature-2
content type line 23
ObjectType-Article-2
ISSN:1010-061X
1420-9101
1420-9101
DOI:10.1111/j.1420-9101.2011.02254.x