Abstract

BackgroundThe critical role of Major Histocompatibility Complex (Mhc) genes in disease resistance and their highly polymorphic nature make them exceptional candidates for studies investigating genetic effects on survival, mate choice and conservation. Species that harbor many Mhc loci and high allelic diversity are particularly intriguing as they are potentially under strong selection and studies of such species provide valuable information as to the mechanisms maintaining Mhc diversity. However comprehensive genotyping of complex multilocus systems has been a major challenge to date with the result that little is known about the consequences of this complexity in terms of fitness effects and disease resistance.ResultsIn this study, we genotyped the Mhc class I exon 3 of the great tit (Parus major) from two nest-box breeding populations near Oxford, UK that have been monitored for decades. Characterization of Mhc class I exon 3 was adopted and bidirectional sequencing was carried using the 454 sequencing platform. Full analysis of sequences through a stepwise variant validation procedure allowed reliable typing of more than 800 great tits based on 214,357 reads; from duplicates we estimated the repeatability of typing as 0.94. A total of 862 alleles were detected, and the presence of at least 16 functional loci was shown - the highest number characterized in a wild bird species. Finally, the functional alleles were grouped into 17 supertypes based on their antigen binding affinities.ConclusionsWe found extreme complexity at the Mhc class I of the great tit both in terms of allelic diversity and gene number. The presence of many functional loci was shown, together with a pseudogene family and putatively non-functional alleles; there was clear evidence that functional alleles were under strong balancing selection. This study is the first step towards an in-depth analysis of this gene complex in this species, which will help understanding how parasite-mediated and sexual selection shape and maintain host genetic variation in nature. We believe that study systems like ours can make important contributions to the field of evolutionary biology and emphasize the necessity of integrating long-term field-based studies with detailed genetic analysis to unravel complex evolutionary processes.

Highlights

  • The critical role of Major Histocompatibility Complex (Mhc) genes in disease resistance and their highly polymorphic nature make them exceptional candidates for studies investigating genetic effects on survival, mate choice and conservation

  • Characterization of great tit Mhc class I exon 3 Amplification of genomic DNA using nine different primer pair combinations yielded three distinct PCR products that differed at the length of exon 3 (282 bp, 276 bp or 273 bp)

  • We found that even the pseudogene alleles were being transcribed, as they were present in the cDNA library

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Summary

Introduction

The critical role of Major Histocompatibility Complex (Mhc) genes in disease resistance and their highly polymorphic nature make them exceptional candidates for studies investigating genetic effects on survival, mate choice and conservation. The Mhc is known to be the most variable gene group in vertebrates, both in terms of allelic diversity and gene number [2]. Differences in the number and organization of Mhc genes are explained by a birth and death model of evolution [11]. According to this model, new genes are formed by duplication events and, while some retain their function in the genome, others are inactivated or deleted [12]. Because an individual Mhc molecule can recognize and bind to a few antigens only, which is determined by the amino acid composition in their antigen-binding site (ABS), gene duplications and polymorphism at the ABS are thought to be adaptations enabling individuals to respond to a greater variety of antigens [13]

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