Structure of genomic DNA in chicken populations revealed by multilocus DNA probe
- Authors: Terletskiy V.P.1, Tyshchenko V.I.1
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Affiliations:
- Russian Research Institute of Farm Animal Genetics and Breeding
- Issue: Vol 18, No 1 (2023)
- Pages: 105-115
- Section: Genetics and selection of animals
- URL: https://agrojournal.rudn.ru/agronomy/article/view/19869
- DOI: https://doi.org/10.22363/2312-797X-2023-18-1-105-115
- EDN: https://elibrary.ru/WTBNKE
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Abstract
Molecular genetic technologies are taking an increasing place in breeding work to improve existing breeds and populations of chickens, as well as in programs to preserve a valuable gene pool. Small local breeds are a source of valuable genes that can be used in breeding. The aim of this work was to obtain new knowledge about the structure of genomic DNA of six chicken populations using multilocus analysis with a labeled molecular probe (GTG)5. Multilocus analysis using labeled DNA probes provides working simultaneously with a large number of genetic loci and calculating population genetic parameters both within populations and between them. The data on use of the multilocus probe (GTG)5 in molecular hybridization reaction in six breeds and populations of chickens were analyzed. The results revealed a large genetic distance between Black-and-White Australorp and the Bald-necked chickens (D = 0.155). Bald-necked chickens are bred in isolation from other breeds to maintain the unique trait of ‘naked necks’. According to the criterion of average heterozygosity, the population of Bald-necked chickens surpassed the Yurlov Crowers and Black-and-White Australorps. Obviously, this is due to the intensive breeding work carried out in the last two populations, which reduces genetic diversity. Marker DNA fragments specific for individual breeds were identified. The effectiveness of multilocus analysis as a tool for identifying the features of genome organization in chicken breeds and populations was confirmed.
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Fig. 1. Outline of main experimental stages of multilocus analysis
Table 1
Population and genetic parameters in 3 chicken populations (Yurlov Crowers, Black-and-White Australorp and Bald-necked chickens) generated by DNA fingerprinting
Chicken population | n | Bands per lane, | P | BS1 | BS2 | D |
Yurlov Crowers Black-and- White Australorp | 10 11 | 27.7 ± 0.9 27.4 ± 0.5 | 9.2 × 10–13 6.9 × 10–12 | 0.37 0.39 | 0.29 | 0.090 |
Yurlov Crowers Bald-necked chickens | 10 11 | 27.7 ± 0.9 22.7 ± 1.6 | 9.2 × 10–13 4.6 × 10–12 | 0.37 0.32 | 0.20 | 0.145 |
Black-and- White Australorp Bald-necked chickens | 11 11 | 27.4 ± 0.5 22.7 ± 1.6 | 6.9 × 10–12 4.6 × x10–12 | 0.39 0.32 | 0.20 | 0.155 |
Note. P — the probability of occurrence of two individuals with an identical set of all DNA fragments; BS1 — coefficient of similarity within groups; BS2 — coefficient of similarity between groups; D — genetic distance.
Table 2
Specific DNA fragments and alleles with different frequency of occurrence in 3 chicken populations (Yurlov Crower, Black-and-White Australorp and Bald-necked chicken) calculated by DNA fingerprinting
DNA fragment | DNA fragment frequ | ency | Frequency of allele occurrence q = 1 — √1 — p | |||
I | II | III | I | II | III | |
85 | 0.80 | 0.27 | 0.18 | 0.55 | 0.15 | 0.09 |
106 | 0.10 | 0.00 | 0.73 | 0.05 | 0.00 | 0.48 |
108 | 0.60 | 0.91 | 0.00 | 0.37 | 0.68 | 0.00 |
112 | 0.00 | 0.91 | 0.18 | 0.00 | 0.05 | 0.09 |
Note. I — Yurlov Crower; II — Black-and-W hite Australorp; III — Bald-necked chicken; p — frequency of DNA fragment in population.
Table 3
Heterozygosity (H) in three chicken populations: Yurlov Crower, Black-and-White Australorp and Bald-necked chicken
Chicken population | n | Number of loci | Number of alleles | Number of polymorphic loci | H |
Yurlov Crower | 10 | 16.16 | 5.88 | 1.00 | 0.71 |
Black-and-White Australorp | 11 | 16.05 | 5.48 | 1.00 | 0.71 |
Bald-necked chicken | 11 | 12.91 | 6.50 | 1.00 | 0.76 |
Fig. 2. Phylogenetic tree showing genetic relationships in chicken breeds according to the Statistica 6.0™ program (Cluster analysis module): Var1 — Yurlov Crowers, Var2 — Black-and-White Australorp, Var3 — Bald-necked chicken. On the y-axis — conventional units of genetic distance
Table 4
Population and genetic parameters in 3 groups of Pavlov chickens (RRIFAGB, Moscow region, Barnaul), as revealed by DNA fingerprinting
Chiken group | n | Bands per lane, | Р | BS1 | BS2 | D |
Pavlov RRIFAGB Pavlov Moscow region | 15 12 | 10.6 ± 0.9 13.6 ± 0.9 | 4.7 × 10–5 5.5 × 10–4 | 0.39 0.58 | 0.43 | 0.055 |
Pavlov RRIFAGB Pavlov Barnaul | 15 13 | 10.6 ± 0.9 15.0 ± 1.4 | 4.7 × 10–5 7.5 × 10–5 | 0.39 0.53 | 0.36 | 0.100 |
Pavlov Moscow region Pavlov Barnaul | 12 13 | 13.6 ± 0.9 15.0 ± 1.4 | 5.5 × 10–4 7.5 × 10–5 | 0.58 0.53 | 0.45 | 0.105 |
About the authors
Valeriy P. Terletskiy
Russian Research Institute of Farm Animal Genetics and Breeding
Author for correspondence.
Email: valeriter@mail.ru
ORCID iD: 0000-0003-4043-3823
SPIN-code: 4512-5328
Doctor of Biological Sciences, Professor, Chief Researcher, Laboratory of Molecular Genetics, Russian Research Institute of Farm Animal Genetics and Breeding
55a Moskovskoe highway, Tyarlevo vil., Pushkin, St. Petersburg, 196625, Russian FederationValentina I. Tyshchenko
Russian Research Institute of Farm Animal Genetics and Breeding
Email: tinatvi@mail.ru
ORCID iD: 0000-0003-4964-9938
SPIN-code: 6294-2400
Candidate of Biological Sciences, Senior Researcher, Laboratory of Molecular Genetics, Russian Research Institute of Farm Animal Genetics and Breeding
55a Moskovskoe highway, Tyarlevo vil., Pushkin, St. Petersburg, 196625, Russian FederationReferences
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