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Genetic Diversity and Variety Identification Study of Pigeon (Columba livia) with COI Gene |
LU Jun-Xian, JIA Xiao-Xu, FU Sheng-Yong, TANG Xiu-Jun, FAN Yan-Feng, GE Qing-Lian, BU Zhu, GAO Yu-Shi* |
Jiangsu Institute of Poultry Science, Yangzhou 225125, China |
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Abstract In China, the pigeon (Columba livia) production ranks fourth after the production of chickens (Gallus gallus), ducks (Anas platyrhynchos), and geese (Anser cygnoides orientalis). The pigeon has many valuable characters, such as high nutritional value and fast growth rate. However, little information is available about the genetic diversity of the pigeons used for agricultural production. The study on the genetic diversity and variety identification of the pigeon is of great significance for genetic conservation and inbreeding programs. The sequence of the mitochondrial cytochrome oxidase subunit Ⅰ (COI) has proven to be useful for the study of the population genetics of domestic animals. For this study, the complete COI gene sequences of 60 pigeons from three breeds (White Feather King, Thaxon, and Silver King) were analyzed. Other COI gene sequences were downloaded from GenBank, including pigeon species from other countries including the rock pigeon (Columba rupestris). No insertions or deletions were found in the COI gene. The sequence read length was 1551 bp, and encoded 517 amino acids. The average nucleotide composition was 25.6% T, 32.1% A, 26.1% C, and 16.2% G, and the content of AT (51.7%) was significantly higher than that of GC (48.3%), indicating slight base bias. Seven polymorphic sites were identified, representing 0.45% of the total analyzed sites. Six haplotypes were identified in 60 pigeons from the 3 investigated populations. The most common haplotype was Hap1, which was present in 26 out the 60 birds and had a frequency of 43.3%. The next-widespread haplotype was Hap 2 with a frequency of 25.0%. Two haplotypes were population-specific: Hap 4 for the White Feather King, Hap 5 for the Silver King pigeon. The overall haplotype diversity was 0.726±0.038. The highest haplotype diversity was found in the Silver King pigeon (0.716±0.069) whereas the lowest diversity was found in the White Feather King pigeon (0.674±0.049). The nucleotide diversity was 0.000 98±0.000 44 across the three investigated breeds, ranging from 0.000 54±0.000 27 in the White Feather King to 0.001 16±0.000 45 in the Silver King pigeon. The overall mean number of nucleotide differences was 1.518. The highest haplotype diversity was found in the Silver King Pigeon (1.795) and the lowest diversity was found in the White Feather King Pigeon (0.842). Based on the COI gene sequences of the 6 haplotypes obtained in this study, and other COI gene sequences, downloaded from GenBank, the rock pigeon (C. rupestris) was used as outgroup, and the molecular phylogenetic tree was constructed by the neighbor-joining method, based on the Kimura-2 parameter mode. Phylogenetic analysis showed that pigeons clustered into 2 cades (A and B). Only one haplotype (Hap 3) was distributed in Clade B, while all other sequences were clustered in Clade A. The median-joining network was constructed using the six haplotypes identified in this study, and the obtained haplotype network showed a star-like phylogeny. Most of the haplotypes were closely related to the common central haplotype (Hap 1), thus suggesting population expansion. The results of this study indicated that the COI gene sequence of pigeons was relatively conservative and contained few mutation sites. This was less effective for the identification of different pigeon breeds. Consequently, there was a high need to incorporate multiple molecular markers such as single nucleotide polymorphism (SNP), simple sequence repeat (SSR), and copy number variations (CNV). The COI gene could be used as a candidate molecular marker to investigate the genetic diversity and origin of pigeon species, and can thus serve as a factual and comparative basis for similar studies in the future.
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Received: 12 January 2020
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Corresponding Authors:
* , gaoys100@sina.com
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[1] 付胜勇, 刘宏祥, 谢鹏, 等. 2015. 中国部分鸽mtDNAD-loop区遗传多态性与系统进化分析[J]. 江苏农业科学, 43(4): 41-43. (Fu S Y, Liu H X, Xie P, et al.2015. Study on mtDNA genetic diversity and phylogenetic relationship of Chinese pigeons[J]. Jiangsu Agricultural Sciences, 43(4): 41-43.) [2] 高玉时, 贾晓旭, 唐修君, 等. 2015. 基于线粒体基因组D-loop区全序列分析安义瓦灰鸡遗传多样性及其起源进化关系[J]. 农业生物技术学报, 23(7): 940-944. (Gao Y S, Jia X X, Tang X J, et al.2015. The genetic diversity and origin analysis of Anyi Tile-like chickens (Gallus gallus domestiaus) based on mitochondrial DNA D-loop sequence[J]. Journal of Agricultural Biotechnology, 23(7): 940-944.) [3] 高玉时, 唐修君, 屠云洁, 等. 2011. 基于线粒体COI基因15个鸡种的DNA编码研究[J]. 中国农业科学, 44(3): 587-594. (Gao Y S, Tang X J, Tu Y J, et al.2011. Studies on the DNA barcoding of fifteen chicken breeds by mtDNA COI gene[J]. Scientia Agricultura Sinica, 44(3): 587-594.) [4] 胡永胜, 方梅霞, 何丹林, 等. 2010. 鸽mtDNA遗传多样性及系统进化研究[J]. 中国家禽, 2(14):23-26. (Hu Y S, Fang M X, He D L, et al.2010. Study on mtDNA genetic diversity and phylogenetic relationship of pigeons[J]. China Poultry, 2(14): 23-26.) [5] 黄勋和, 陈洁波, 何丹林, 等. 2016. DNA条形码技术鉴定中国地方鸡品种的重新评估[J]. 中国农业科学, 49(13):2622-2633. (Huang X H, Chen J B, He D L, et al.2016. DNA barcoding of indigenous chickens in China: A reevaluation[J]. Scientia Agricultura Sinica, 49(13): 2622-2633.) [6] 贾晓旭. 2009. 鸽生长激素(GH)基因多态性及其与早期体重和屠宰性状的关联分析[D]. 硕士学位论文, 南京农业大学, 导师: 杜文兴, pp. 1-3. (Jia X X.2009. Analysis on polymorphism of GH gene and its relationship with early body weight and carcass traits in pigeon)[D]. Thesis for M. S., Nanjing Agricultural University, Supervisor: Du W X, pp. 1-3.) [7] 贾晓旭, 牛鲜艳, 何宗亮, 等. 2010. 利用羽毛对鸽子进行分子性别鉴定[J]. 农业生物技术学报, 18(5): 1019-1023. (Jia X X, Niu X Y, He Z L, et al.2010. Sex identification of pigeon by extracting DNA from its feather[J]. Journal of Agricultural Biotechnology, 18(5): 1019-1023.) [8] 贾晓旭, 唐修君, 樊艳凤, 等. 2017. 华东地区地方鸡品种mtDNA控制区遗传多样性[J]. 生物多样性, 25(5): 540-548. (Jia X X, Tang X J, Fan Y F, et al.2017. Genetic diversity of local chicken breeds in east China based on mitochondrial DNA D-loop region[J]. Biodiversity Science, 25(5): 540-548.) [9] 武艳平, 霍俊宏, 刘林秀, 等. 2011. 江西地方鸡的系统进化及遗传多样性研究[J]. 江西农业大学学报, 33(6): 1160-1163. (Wu Y P, Huo J H, Liu L X, et al.2011. Diversity and phylogenetic relationships of Jiangxi chicken breeds[J]. Journal of Jiangxi Agricultural University, 33(6): 1160-1163.) [10] Bandelt H J, Forster P, Röhl A.1999. Median-joining networks for inferring intraspecific phylogenies.[J]. Molecular Biology & Evolution, 16(1): 37. [11] Craft K J, Pauls S U, Darrow K, et al.2010. Population genetics of ecological communities with DNA barcodes: An example from New Guinea Lepidoptera[J]. Proceedings of the National Academy of Sciences of the USA, 107(11): 5041-5046. [12] Hebert P D N, Ratnasingham S, Waard J R D.2003. Barcoding animal life: Cytochrome c oxidase subunit 1 divergences among closely related species[J]. Proceedings of the Royal Society B-Biological Sciences, 270 Suppl (Suppl): S96-S99. [13] Hebert P D N, Stoeckle M Y, Zemlak T S, et al.2004. Identification of birds through DNA barcodes[J]. PLoS Biology, 2(10): e312. [14] Murphy R W, Crawford A J, Bauer A M, et al.2013. Cold Code: The global initiative to DNA barcode amphibians and nonavian reptiles[J]. Molecular Ecology Resources, 13(2): 161-167. [15] Rozas J, Sanchezelbarrio J C, Messeguer X, et al.2003.DnaSP, DNA polymorphism analyses by the coalescent and other methods[J]. Bioinformatics, 19(18): 2496-2497. [16] Shen Y Y, Chen X, Murphy R W.2013. Assessing DNA barcoding as a tool for species identification and data quality control[J]. PLOS ONE, 8(2): e57125. [17] Tamura K, Stecher G, Peterson D, et al.2013. MEGA6: Molecular evolutionary genetics analysis, version 6.0. Molecular Biology and Evolution[J]. 30(12): 2725-2729. [18] Thompson J D, Gibson T J, Plewniak F, et al.1997. The ClustalX windows interface: Flexible strategies for multiple sequence alignment aided by quality analysis tools[J]. Nucleic Acids Research, 25(25): 4876-4882. [19] Ward R D, Zemlak T S, Innes B H, et al.2005. DNA barcoding Australia's fish species[J]. Proceedings of the Royal Society B: Biological Sciences, 360(1462): 1847-1857. [20] Xiang H, Gao J Q, Yu B Q, et al.2014. Early Holocene chicken domestication in northern China[J]. Proceedings of the National Academy of Sciences of the USA, 111(49): 17564-17569. |
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