摘要
<span style="font-family:Verdana;">The Tswana chicken is native to Botswana and comprises strains such as the naked neck, normal, dwarf, frizzled</span><span style="font-family:Verdana;">,</span><span style="font-family:;" "=""><span style="font-family:Verdana;"> and rumples. </span><span style="font-family:Verdana;">The origins of the different strain</span><span style="font-family:Verdana;">s of Tswana chicken remain unknown and it is not yet clear if the different</span><span style="font-family:Verdana;"> strains represent distinct breeds within the large Tswana chicken population. Genetic characterization of different strains of Tswana chickens using SNP arrays can elucidate their genetic relationships and ascertain if the strains represent distinct breeds</span></span><span style="font-family:Verdana;"> of</span><span style="font-family:Verdana;"> Tswana chicken population. The aim of this study was therefore to investigate population structure and diversity and to estimate genetic distances/identity between the naked neck, normal and dwarf strains of Tswana chickens. A total of 96 chickens </span><span style="font-family:Verdana;">(</span><span style="font-family:Verdana;">normal strain (n = 39), naked neck strain (n = 32), dwarf strain (n = 13) and </span><span style="font-family:Verdana;">commercial</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">broiler (n = 12)</span><span style="font-family:Verdana;">)</span><span style="font-family:;" "=""><span style="font-family:Verdana;"> were used in the study. SNP genotyping was carried out using the Illumina chicken iSelect SNP 60 Bead chip using the Infinium assay compatible with the Illumina HiScan SQ genotyping platform. The observed heterozygosity (H</span><sub><span style="font-family:Verdana;">o</span></sub><span style="font-family:Verdana;">) values were 0.610 ± 0.012, 0.611 ± 0.014, 0.613 ± 0.0006 for normal, naked neck and dwarf strains of Tswana chickens respectively and averaged 0.611 ± 0.016 across the three strains of Tswana chickens compared to Ho of 0.347 ± 0.023 in commercial broiler chicken. The expected heterozygosity (H</span><sub><span style="font-family:Verdana;">e</span></sub><span style="font-family:Verdana;">) values were 0.613 ± 0.00012, 0.614 ± 0.00013, 0.608 ± 0.00021 for normal, naked neck and dwarf strains of Tswana chickens respectively and averaged 0.612 ± 0.00015 across the three strains of Tswana chickens compared to H</span><sub><span style="font-family:Verdana;">e</span></sub><span style="font-family:Verdana;"> of 0.577 ± 0.00022 in commercial broiler chicken. Principal component analysis (PCA) was used to get an insight into the population structure of indigenous Tswana chickens. The first two principal components revealed a set of three clusters. The normal strain of Tswana chicken and commercial broiler clustered together in one group. The dwarf strain clustered separately in one group and the naked neck and normal strains clustered together in the last group. The separate clustering of the dwarf strain from the rest of Tswana chicken strains suggests significant genetic uniqueness of the dwarf strain and very close genetic similarities between the normal and naked neck strains. </span><span style="font-family:Verdana;">The clustering pattern was confirmed by less genetic differentiation and less genetic distances between the naked neck and normal strains of Tswana chicken than between the two strains and the dwarf strain of Tswana chicken.</span></span>
<span style="font-family:Verdana;">The Tswana chicken is native to Botswana and comprises strains such as the naked neck, normal, dwarf, frizzled</span><span style="font-family:Verdana;">,</span><span style="font-family:;" "=""><span style="font-family:Verdana;"> and rumples. </span><span style="font-family:Verdana;">The origins of the different strain</span><span style="font-family:Verdana;">s of Tswana chicken remain unknown and it is not yet clear if the different</span><span style="font-family:Verdana;"> strains represent distinct breeds within the large Tswana chicken population. Genetic characterization of different strains of Tswana chickens using SNP arrays can elucidate their genetic relationships and ascertain if the strains represent distinct breeds</span></span><span style="font-family:Verdana;"> of</span><span style="font-family:Verdana;"> Tswana chicken population. The aim of this study was therefore to investigate population structure and diversity and to estimate genetic distances/identity between the naked neck, normal and dwarf strains of Tswana chickens. A total of 96 chickens </span><span style="font-family:Verdana;">(</span><span style="font-family:Verdana;">normal strain (n = 39), naked neck strain (n = 32), dwarf strain (n = 13) and </span><span style="font-family:Verdana;">commercial</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">broiler (n = 12)</span><span style="font-family:Verdana;">)</span><span style="font-family:;" "=""><span style="font-family:Verdana;"> were used in the study. SNP genotyping was carried out using the Illumina chicken iSelect SNP 60 Bead chip using the Infinium assay compatible with the Illumina HiScan SQ genotyping platform. The observed heterozygosity (H</span><sub><span style="font-family:Verdana;">o</span></sub><span style="font-family:Verdana;">) values were 0.610 ± 0.012, 0.611 ± 0.014, 0.613 ± 0.0006 for normal, naked neck and dwarf strains of Tswana chickens respectively and averaged 0.611 ± 0.016 across the three strains of Tswana chickens compared to Ho of 0.347 ± 0.023 in commercial broiler chicken. The expected heterozygosity (H</span><sub><span style="font-family:Verdana;">e</span></sub><span style="font-family:Verdana;">) values were 0.613 ± 0.00012, 0.614 ± 0.00013, 0.608 ± 0.00021 for normal, naked neck and dwarf strains of Tswana chickens respectively and averaged 0.612 ± 0.00015 across the three strains of Tswana chickens compared to H</span><sub><span style="font-family:Verdana;">e</span></sub><span style="font-family:Verdana;"> of 0.577 ± 0.00022 in commercial broiler chicken. Principal component analysis (PCA) was used to get an insight into the population structure of indigenous Tswana chickens. The first two principal components revealed a set of three clusters. The normal strain of Tswana chicken and commercial broiler clustered together in one group. The dwarf strain clustered separately in one group and the naked neck and normal strains clustered together in the last group. The separate clustering of the dwarf strain from the rest of Tswana chicken strains suggests significant genetic uniqueness of the dwarf strain and very close genetic similarities between the normal and naked neck strains. </span><span style="font-family:Verdana;">The clustering pattern was confirmed by less genetic differentiation and less genetic distances between the naked neck and normal strains of Tswana chicken than between the two strains and the dwarf strain of Tswana chicken.</span></span>