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Gene Silencing of Mink (Neovison vison) Agouti Induced by 601 bp SINE Insertion Mutation |
LI Lan-Hui1,3*, DU Xiao-Long1*, WANG Qi1, ZHANG Le-Chao1, GE Lin-Han1, ZHOU Rong-Yan1, LI Xue-Mei1, LI Xiang-Long2** |
1 College of Animal Science and Technology, Hebei Agricultural University, Baoding 071001, China; 2 Hebei Normal University of Science & Technology, Qinhuangdao 066600, China; 3 Research Center of Cattle and Sheep Embryo Engineering Technique of Hebei, Baoding 071001, China |
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Abstract Agouti-signaling protein (ASIP), encoded by Agouti and acted as an antagonist of Melanocortin 1-receptor (MC1R), plays a key role in inhibiting deposition of eumelanin and forming the coat color of tan striped character. Mink (Neovison vison) has a colorful coat and is an important economic animal for fur. However, the role of Agouti in mink coat color is unclear. To get the Agouti gene sequence of mink and its structure character, the distribution of 601 bp insertion mutation and the relationship between transcription of fragment with insertion and Agouti gene was explored. The genome of black mink, white mink and coffee mink and the RNA from skin of black mink and coffee mink were used to amplify Agouti gene sequence and transcriptome sequencing, respectively. PCR cloning and sequencing, and bioinformatics analysis were used to get Agouti gene sequence and mutations, respectively. And the spliceosome types were predicted. Population analysis was done for the 601 bp insertion in the three-color-type mink, and the luciferase promoter activity was detected for fragments in both directions with and without the 601 bp insertion. The transcripts of Agouti gene were analyzed based on the transcriptome of mink skin. The mink Agouti gene sequence for 25 478 bp was submitted to NCBI (GenBank No. KP981640.1) and 7 spliceosomes were predicted. 60 SNPs and Short interspersed nuclear element (SINE), a 601 bp insertion mutation were found in Agouti gene. The wild genotype frequency in black mink was significantly higher than white mink and coffee mink (P<0.05). The promoter activity of the 1 605 bp fragment in forward direction, which included the SINE and the up and down stream sequence of the insertion locus, was significantly higher than that of the fragments in inverse direction and the deletion fragments in both directions (P<0.01). A 973 bp transcript contained the 601 bp SINE was 100% covered and similar with the intron 3 sequence of Agouti gene. However, none of the Agouti transcripts was detected. It was concluded that the Agouti transcription was silenced by the 601 bp SINE insertion in the intron 3 of Agouti gene, and the insertion fragments had promoter activity and the transcript. The research discovered that Agouti gene might not take part in the coat color formation of mink, which provides some data for further studying relationship between expression regulation of transposable elements and gene function.
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Received: 06 July 2018
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Corresponding Authors:
**, lixianglongcn@yahoo.com
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About author:: *Authors who contribute equally |
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[1] 李英杰, 刘铮铸, 巩元芳等. 2015. 狐狸Agouti基因SNPs筛查及其与毛色关联性分析[J]. 畜牧兽医学报, 46(9): 1692-1696. (Li Y J, Liu Z Z, Gong Y F, et al.2015. SNPs detection of Agouti gene and its association with coat color in fox[J]. Acta Veterinaria et Zootechnica Sinica, 46(9): 1692-1696.) [2] 宋兴超, 徐超, 刘宗岳, 等. 2016. 美洲水貂刺鼠信号蛋白基因SNPs检测及其与毛色表型的关联分析[J]. 畜牧兽医学报, 47(4): 723-732. (Song X C, Xu C, Liu Z Y, et al.2016. Single nucleotide polymorphisms detetion of Agouti gene and its association with coat color phenotype in American mink (Neovison vison)[J]. Acta Veterinaria et Zootechnica Sinica, 47(4): 723-732.) [3] Anistoroaei R, ten Hallers B, Nefedov M, et al.2011. Construction of an American mink bacterial artificial chromosome (BAC) library and sequencing candidate genes important for the fur industry[J]. BMC Genomics, 12(9): 354. [4] Anistoroaei R, Markakis M N, Vissenberg K, et al.2012. Exclusion of candidate genes for coat colour phenotypes of the American mink (Neovison vison)[J]. Animal Genetics, 43(6): 813-816. [5] Bultman S J, Michaud E J, Woychik R P.1992. Molecular characterization of the mouse agouti locus[J]. Cell, 71(7): 1195-1204. [6] Campana M G, Parker L D, Hawkins M T, et al.2016. Genome sequence, population history, and pelage genetics of the endangered African wild dog (Lycaon pictus)[J]. BMC Genomics, 17(1): 1013-1022. [7] Casacuberta E, González J.2013. The impact of transposable elements in environmental adaptation[J]. Molecular Ecology, 22(6): 1503-1517. [8] Cerdá-Reverter J M, Haitina T, Schiöth H B, et al.2005. Gene structure of the goldfish agouti-signaling protein: A putative role in the dorsal-ventral pigment pattern of fish[J]. Endocrinology, 146(3): 1597-1610. [9] Chuong E B, Elde N C, Feschotte C.2017. Regulatory activities of transposable elements: From conflicts to benefits[J]. Nature Reviews Genetics, 18(2): 71-86. [10] Ciampolini R, Cecchi F, Spaterna A, et al.2013. Characterization of different 5'-untranslated exons of the ASIP gene in black-and-tan Doberman Pinscher and brindle Boxer dogs[J]. Animal Genetics, 44(1): 114-117. [11] Cordaux R, Batzer M A.2009. The impact of retrotransposons on human genome evolution[J]. Genetics, 10(10): 691-713. [12] Dreger D L, Parker H G, Ostrander E A, et al.2013. Identification of a mutation that is associated with the saddle tan and black-and-tan phenotypes in Basset Hounds and Pembroke Welsh Corgis[J]. Journal of Heredity, 104(3): 399-406. [13] Girardot M, Guibert S, Laforet M P, et al.2006. The insertion of a full-length Bos taurus LINE element is responsible for a transcriptional deregulation of the Normande Agouti gene[J]. Pigment Cell Research, 19(4): 346-355. [14] Kohany O, Gentles A J, Hankus L, et al.2006. Annotation, submission and screening of repetitive elements in Repbase: RepbaseSubmitter and Censor[J]. BMC Bioinformatics, 7(10): 474. [15] Li M H, Tiirikka T, Kantanen J.2014. A genome-wide scan study identifies a single nucleotide substitution in ASIP associated with white versus non-white coat-colour variation in sheep (Ovis aries)[J]. Heredity, 112(2): 122-131. [16] Stoltzfus A, Norris R W.2016. On the causes of evolutionary transition: Transversion bias[J]. Molecular Biology and Evolution, 33(3): 595-602. [17] Tanaka Y, Chung L, Park I H.2012. Impact of retrotransposons in pluripotent stem cells[J]. Molecules and Cells, 34(6): 509-516. [18] Wang J, Xie G, Singh M, et al.2014. Primate-specific endogenous retrovirus-driven transcription defines naive-like stem cells[J]. Nature, 516(7531): 405-409. [19] Weikard R, Hadlich F, Kuehn C.2013. Identification of novel transcripts and noncoding RNAs in bovine skin by deep next generation sequencing[J]. BMC Genomics, 14(9): 789. |
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