Abstract

BackgroundThe availability of larger-scale SNP data sets in the chicken genome allows to achieve a higher resolution of the pattern of linkage disequilibrium (LD). In this study, 36 k and 57 k genotypes from two independent genotyping chips were used to systematically characterize genome-wide extent and structure of LD in the genome of four chicken populations. In total, we analyzed genotypes of 454 animals from two commercial and two experimental populations of white and brown layers which allows to some extent a generalization of the results.ResultsThe number of usable SNPs in this study was 19 k to 37 k in brown layers and 8 k to 19 k in white layers. Our analyzes showed a large difference of LD between the lines of white and brown layers. A mean value of r2 = 0.73 ± 0.36 was observed in pair-wise distances of < 25 Kb for commercial white layers, and it dropped to 0.60 ± 0.38 with distances of 75 to 120 Kb, the interval which includes the average inter-marker space in this line. In contrast, an overall mean value of r2= 0.32 ± 0.33 was observed for SNPs less than 25 Kb apart from each other and dropped to 0.21 ± 0.26 at a distance of 100 kb in commercial brown layers. There was a remarkable similarity of the LD patterns among the two populations of white layers. The same was true for the two populations of brown layers, while the LD pattern between white and brown layers was clearly different. Inferring the population demographic history from LD data resulted in a larger effective population size in brown than white populations, reflecting less inbreeding among brown compared to white egg layers.ConclusionsWe report comprehensive LD map statistics for the genome of egg laying chickens with an up to 3 times higher resolution compared to the maps available so far. The results were found to be consistent between analyzes based on the parallel SNP chips and across different populations (commercial vs. experimental) within the brown and the white layers. It is concluded that the current density of usable markers in this study is sufficient for association mapping and the implementation of genomic selection in these populations to achieve a similar accuracy as in implementations of association mapping and genomic selection in mammalian farm animals.

Highlights

  • The availability of larger-scale single nucleotide polymorphisms (SNPs) data sets in the chicken genome allows to achieve a higher resolution of the pattern of linkage disequilibrium (LD)

  • As in many other species, microsatellites recently have been replaced by single nucleotide polymorphisms (SNPs) and maps based on high-density SNP arrays reveal much lower levels of LD, limited to ≤ 100 kb [9,10,11]

  • The results were found to be consistent between analyses based on the parallel SNP chips, indicating that results were independent of the panel used, as expected when SNPs are neutral and most LD is generated by drift (Figure 7)

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Summary

Introduction

The availability of larger-scale SNP data sets in the chicken genome allows to achieve a higher resolution of the pattern of linkage disequilibrium (LD). Information on the extent of LD in genomic regions harboring quantitative trait loci (QTLs) is necessary for effective applications of marker assisted selection in commercial breeding recombination variability and blocking structure is of key importance for the genome-based analysis of population history and for the fine-tuning of applications like association mapping and genomic selection. Since the first genetic linkage map of chicken was published by Serebrovsky and Petrov [5] several versions of linkage maps, mostly based on microsatellite markers, have been constructed [6,7,8]. These studies have reported substantial LD over long distances for pairs of loci being up to 5 cM apart. The latest map included 13,340 markers with a total map length of 3,054 cM in broilers [12]

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