Structure of genomic DNA in chicken populations revealed by multilocus DNA probe

V. Terletskiy, V. Tyshchenko
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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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用多位点DNA探针分析鸡群体基因组DNA结构
分子遗传技术在育种工作中发挥着越来越重要的作用,以改善现有的鸡品种和种群,以及保护有价值的基因库。小型地方品种是可用于育种的宝贵基因的来源。本工作的目的是利用标记分子探针(GTG)对6个鸡种群的基因组DNA结构进行多位点分析。使用标记DNA探针进行多位点分析,可以同时处理大量的遗传位点,并计算群体内和群体之间的群体遗传参数。分析了多位点探针(GTG)5在6个鸡品种和群体分子杂交反应中的应用情况。结果表明,黑白Australorp与秃颈鸡有较大的遗传距离(D = 0.155)。秃头鸡是与其他品种隔离饲养的,以保持秃头鸡的独特特征。以平均杂合度为标准,秃颈鸡的种群数量超过了乌尔洛乌和黑白australorp。显然,这是由于在最后两个种群中进行的密集育种工作,这降低了遗传多样性。鉴定了个别品种特有的标记DNA片段。多位点分析作为鉴定鸡品种和群体基因组组织特征的有效工具得到了证实。
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审稿时长
12 weeks
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