[1] 中国畜禽遗传资源委员会.中国畜禽遗传资源志——马驴驼志[M].北京:中国农业出版社,2011.CHINA NATIONAL COMISSION OF ANIMAL GENETICS RESOURCES.Animal Genetics Resource in China——Horses,Donkeys and Camels[M].Beijing:China Agriculture Press,2011.(in Chinese)
[2] 韩国才.传统马业与现代马业[J].中国畜牧杂志,2004,40(12):33-35.HAN G C.Traditional horse industry and modern horse industry[J].Chinese Journal of Animal Science,2004,40(12):33-35.(in Chinese)
[3] 魏珣,贾敬敦,孙康泰,等.基于文献计量的世界家畜种业科技创新研究态势分析[J].中国农业科学,2015,48(13):2622-2634.WEI X,GUO J D,SUN K T,et al.A bibliometric analysis on technology innovation of livestock breeding[J].Scientia Agricultura Sinica,2015,48(13):2622-2634.(in Chinese)
[4] WADE C M,GIULOTTO E,SIGURDSSON S,et al.Genome sequence,comparative analysis,and population genetics of the domestic horse[J].Science,2009,326(5954):865.
[5] JÍNSSON H,SCHUBERT M,SEGUIN-ORLANDO A,et al.Speciation with gene flow in equids despite extensive chromosomal plasticity[J].Proceedings of the National Academy of Sciences,2014,111(52):18655.
[6] HUANG J L,ZHAO Y P,BAI D Y,et al.Donkey genome and insight into the imprinting of fast karyotype evolution[J].Scientific Reports,2015,5:14106.
[7] RENAUD G,PETERSEN B,SEGUIN-ORLANDO A,et al.Improved de novo genomic assembly for the domestic donkey[J].Science Advances,2018,4(4):eaaq0392.
[8] SCHUELKE M,WAGNER K R,STOLZ L E,et al.Myostatin mutation associated with gross muscle hypertrophy in a child[J].New England Journal of Medicine,2004,350(26):2682-2688.
[9] MCPHERRON A C,LAWLER A M,LEE S J.Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member[J].Nature,1997,387(6628):83.
[10] MCPHERRON A C,LEE S J.Double muscling in cattle due to mutations in the myostatin gene[J].Proceedings of the National Academy of Sciences,1997,94(23):12457-12461.
[11] MARCQ F,ELSEN J M,EL BARKOUKI S,et al.Investigating the role of myostatin in the determinism of double muscling characterizing Belgian Texel sheep[J].Animal Genetics,1998,29(Suppl 1):52.
[12] MCGIVNEY B A,BROWNE J A,FONSECA R G,et al.MSTN genotypes in Thoroughbred horses influence skeletal muscle gene expression and racetrack performance[J].Animal Genetics,2012,43(6):810-812.
[13] BROOKS S A,BAILEY E.Exon skipping in the KIT gene causes a Sabino spotting pattern in horses[J].Mammalian Genome,2005,16(11):893-902.
[14] COSENZA G,PAUCIULLO A,ANNUNZIATA A L,et al.Identification and characterization of the donkey CSN1S2Ⅰ and Ⅱ cDNAs[J].Italian Journal of Animal Science,2010,9(2):206-211.
[15] ZHANG J L,ZAN L S,FANG P,et al.Genetic variation of PRLR gene and association with milk performance traits in dairy cattle[J].Canadian Journal of Animal Science,2008,88(1):33-39.
[16] MAKVANDI-NEJAD S,HOFFMAN G E,ALLEN J J,et al.Four loci explain 83% of size variation in the horse[J].PLoS One,2012,7(7):e39929.
[17] SIGNER-HASLER H,FLURY C,HAASE B,et al.A genome-wide association study reveals loci influencing height and other conformation traits in horses[J].PLoS One,2012,7(5):e37282.
[18] TETENS J,WIDMANN P,KVHN C,et al.A genome-wide association study indicates LCORL/NCAPG as a candidate locus for withers height in German Warmblood horses[J].Animal Genetics,2013,44(4):467-471.
[19] METZGER J,SCHRIMPF R,PHILIPP U,et al.Expression levels of LCORL are associated with body size in horses[J].PLoS One,2013,8(2):e56497.
[20] HE S,ZHANG L,LI W,et al.BIEC2-808543 SNP in the LCORL gene is associated with body conformation in the Yili horse[J].Animal Biotechnology,2015,26(4):289-291.
[21] TOZAKI T,SATO F,ISHIMARU M,et al.Sequence variants of BIEC2-808543 near LCORL are associated with body composition in Thoroughbreds under training[J].Journal of Equine Science,2016,27(3):107-114.
[22] STAIGER E A,AL ABRI M A,PFLUG K M,et al.Skeletal variation in Tennessee walking horses maps to the LCORL/NCAPG gene region[J].Physiological Genomics,2016,48(5):325-335.
[23] TOZAKI T,KIKUCHI M,KAKOI H,et al.A genome-wide association study for body weight in Japanese Thoroughbred racehorses clarifies candidate regions on chromosomes 3,9,15,and 18[J].Journal of Equine Science,2017,28(4):127-134.
[24] TOZAKI T,SATO F,HILL E W,et al.Sequence variants at the myostatin gene locus influence the body composition of Thoroughbred horses[J].Journal of Veterinary Medical Science,2011,73(12):1617-1624.
[25] KADER A,LI Y,DONG K,et al.Population variation reveals independent selection toward small body size in Chinese Debao pony[J].Genome Biology & Evolution,2015,8(1):42-50.
[26] LIU X X,PAN J F,ZHAO Q J,et al.Detecting selection signatures on the X chromosome of the Chinese Debao pony[J].Journal of Animal Breeding & Genetics,2018,135(1):84-92.
[27] FRISCHKNECHT M,JAGANNATHAN V,PLATTET P,et al.A non-synonymous HMGA2 variant decreases height in Shetland ponies and other small horses[J].PLoS One,2015,10(10):e0140749.
[28] METZGER J,GAST A C,SCHRIMPF R,et al.Whole-genome sequencing reveals a potential causal mutation for dwarfism in the Miniature Shetland pony[J].Mammalian Genome,2017,28(3-4):143-151.
[29] HILL E W,GU J,EIVERS S S,et al.A sequence polymorphism in MSTN predicts sprinting ability and racing stamina in thoroughbred horses[J].PLoS One,2010,5(1):e8645.
[30] HILL E W,MCGIVNEY B A,GU J,et al.A genome-wide SNP-association study confirms a sequence variant (g.66493737C>T) in the equine myostatin (MSTN) gene as the most powerful predictor of optimum racing distance for Thoroughbred racehorses[J].BMC Genomics,2010,11:552.
[31] HILL E W,FONSECA R G,MCGIVNEY B A,et al.MSTN genotype (g.66493737 C/T) association with speed indices in Thoroughbred racehorses[J].Journal of Applied Physiology,2012,112(1):86-90.
[32] PETERSEN J L,MICKELSON J R,RENDAHL A K,et al.Genome-wide analysis reveals selection for important traits in domestic horse breeds[J].PLoS Genetics,2013,9(1):e1003211.
[33] GU J,MACHUGH D E,MCGIVNEY B A,et al.Association of sequence variants in CKM (creatine kinase,muscle) and COX4I2(cytochrome c oxidase,subunit 4,isoform 2) genes with racing performance in Thoroughbred horses[J].Equine Veterinary Journal,2010,42(38):569-575.
[34] HILL E W,GU J,MCGIVNEY B A,et al.Targets of selection in the Thoroughbred genome contain exercise-relevant gene SNPs associated with elite racecourse performance[J].Animal Genetics,2010,41(Suppl 2):56-63.
[35] 曹行,何美升,于茜,等.伊犁马PDK4基因多态性与耐力性能的相关性研究[J].新疆农业大学学报,2016,39(4):302-306.CAO H,HE M S,YU X,et al.Polymorphism of PDK4 gene in Yili horse and endurance performance[J].Journal of Xinjiang Agricultural University,2016,39(4):302-306.(in Chinese)
[36] PEREIRA G L,MATTEIS R D,MEIRA C T,et al.Comparison of sequence variants in the PDK4,and COX4I2,genes between racing and cutting lines of Quarter horses and associations with the speed index[J].Journal of Equine Veterinary Science,2015,39:1-6.
[37] RICARD A,ROBERT C,BLOUIN C,et al.Endurance exercise ability in the horse:A trait with complex polygenic determinism[J].Frontiers in Genetics,2017,8:89.
[38] ANDERSSON L S,LARHAMMAR M,MEMIC F,et al.Mutations in DMRT3 affect locomotion in horses and spinal circuit function in mice[J].Nature,2012,488(7413):642-646.
[39] PROMEROVÁ M,ANDERSSON L S,JURAS R,et al.Worldwide frequency distribution of the ‘Gait keeper’ mutation in the DMRT3 gene[J].Animal Genetics,2014,45(2):274-282.
[40] HAN H,ZENG L,DANG R,et al.The DMRT3 gene mutation in Chinese horse breeds[J].Animal Genetics,2015,46(3):341-342.
[41] FEGRAEUS K J,JOHANSSON L,MÄENPÄÄ M,et al.Different DMRT3 genotypes are best adapted for harness racing and riding in finnhorses[J].Journal of Heredity,2015,106(6):734-740.
[42] JÄDERKVIST K,ANDERSSON L S,JOHANSSON A M,et al.The DMRT3 ‘Gait keeper’ mutation affects performance of Nordic and Standardbred trotters[J].Journal of Animal Science,2014,92(10):4279-4286.
[43] SCHRÖDER W,KLOSTERMANN A,STOCK K F,et al.A genome-wide association study for quantitative trait loci of show-jumping in Hanoverian warmblood horses[J].Animal Genetics,2012,43(4):392-400.
[44] BRARD S,RICARD A.Genome-wide association study for jumping performances in French sport horses[J].Animal Genetics,2015,46(1):78-81.
[45] 赵若阳,赵一萍,李蓓,等.马毛色遗传机理研究进展[J].遗传,2018,40(5):357-368.ZHAO R Y,ZHAO Y P,LI B,et al.Overview of the genetic control of horse coat color patterns[J].Hereditas,2018,40(5):357-368.(in Chinese)
[46] 李蓓,何小龙,赵一萍,等.马毛色遗传的分子基础与应用[J].遗传,2010,32(11):1133-1140.LI B,HE X L,ZHAO Y P,et al.Molecular basis and applicability in equine color genetics[J].Hereditas,2010,32(11):1133-1140.(in Chinese)
[47] MARKLUND L,MOLLER M J,SANDBERG K,et al.A missense mutation in the gene for melanocyte-stimulating hormone receptor (MC1R) is associated with the chestnut coat color in horses[J].Mammalian Genome,1996,7(12):895-899.
[48] RIEDER S,TAOURIT S,MARIAT D,et al.Mutations in the agouti (ASIP),the extension (MC1R),and the brown (TYRP1) loci and their association to coat color phenotypes in horses (Equus caballus)[J].Mammalian Genome,2001,12(6):450-455.
[49] TERRY R B,ARCHER S,BROOKS S,et al.Assignment of the appaloosa coat colour gene (LP) to equine chromosome 1[J].Animal Genetics,2004,35(2):134-137.
[50] BELLONE R R,BROOKS S A,SANDMEYER L,et al.Differential gene expression of TRPM1,the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus)[J].Genetics,2008,179(4):1861-1870.
[51] BELLONE R R,FORSYTH G,LEEB T,et al.Fine-mapping and mutation analysis of TRPM1:A candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses[J].Briefings in Functional Genomics,2010,9(3):193-207.
[52] SANDMEYER L S,BELLONE R R,ARCHER S,et al.Congenital stationary night blindness is associated with the leopard complex in the miniature horse[J].Veterinary Ophthalmology,2012,15(1):18-22.
[53] BELLONE R R,ARCHER S,WADE C M,et al.Association analysis of candidate SNPs in TRPM1 with leopard complex spotting (LP) and congenital stationary night blindness (CSNB) in horses[J].Animal Genetics,2010,41(s2):207.
[54] BELLONE R R,HOLL H,SETALURI V,et al.Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse[J].PLoS One,2013,8(10):e78280.
[55] MARKLUND S,MOLLER M,SANDBERG K,et al.Close association between sequence polymorphism in the KIT gene and the roan coat color in horses[J].Mammalian Genome,1999,10(3):283-288.
[56] BROOKS S A,TERRY R B,BAILEY E.A PCR-RFLP for KIT associated with tobiano spotting pattern in horses[J].Animal Genetics,2002,33(4):301-303.
[57] BROOKS S A,LEAR T L,ADERSON D L,et al.A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horses[J].Cytogenetic and Genome Research,2007,119(3-4):225-230.
[58] HAASE B,JUDE R,BROOKS S A,et al.An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds[J].Animal Genetics,2008,39(3):306-309.
[59] HAASE B,BROOKS S A,TOZAKI T,et al.Seven novel KIT mutations in horses with white coat colour phenotypes[J].Animal Genetics,2009,40(5):623-629.
[60] RIEDER S,HAGGER C,OBEXERRUFF G,et al.Genetic analysis of white facial and leg markings in the Swiss Franches-Montagnes horse breed[J].Journal of Heredity,2008,99(2):130-136.
[61] HAASE B,SIGNER-HASLER H,BINNS M M,et al.Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses[J].PLoS One,2013,8(9):e75071.
[62] HAUSWIRTH R,HAASE B,BLATTER M,et al.Mutations in MITF and PAX3 cause "Splashed white" and other white spotting phenotypes in horses[J].PLoS Genetics,2012,8(4):e1002653.
[63] NEGRO S,IMSLAND F,VALERA M,et al.Association analysis of KIT,MITF,and PAX3 variants with white markings in Spanish horses[J].Animal Genetics,2017,48(3):349-352.
[64] ROSENGREN-PIELBERG G,GOLOVKO A,SUNDSTRÖM E,et al.A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse[J].Nature Genetics,2008,40(8):1004-1009.
[65] SUNDSTRÖM E,IMSLAND F,MIKKO S,et al.Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses[J].BMC Genomics,2012,13:365.
[66] 李蓓,何小龙,芒来.蒙古马突触融合蛋白17(STX17)基因多态性及在不同毛色皮肤组织中的表达分析[J].畜牧兽医学报,2011,42(11):1632-1637.LI B,HE X L,MANG L.Analysis on polymorphism and expression in different coat color skin of syntaxin-17(STX17) gene in Mongolian horse[J].Acta Veterinaria et Zootechnica Sinica,2011,42(11):1632-1637.(in Chinese)
[67] BRUNBERG E,ANDERSSON L,COTHRAN G,et al.A missense mutation in PMEL17 is associated with the Silver coat color in the horse[J].BMC Genetics,2006,7:46.
[68] IMSLAND F,MCGOWAN K,RUBIN C J,et al.Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses[J].Nature Genetics,2016,48(2):152-158.
[69] STEFANIUK-SZMUKIER M,ROPKA-MOLIK M,PIÍRKOWSKA K,et al.Variation in TBX3 gene region in Dun coat color Polish Konik horses[J].Journal of Equine Veterinary Science,2017,49:60-62.
[70] DEEG C A,MARTI E,GAILLARD C,et al.Equine recurrent uveitis is strongly associated with the MHC class Ⅰ haplotype ELA-A9[J].Equine Veterinary Journal,2004,36(1):73-75.
[71] KULBROCK M,LEHNER S,METZGER J,et al.A genome-wide association study identifies risk loci to equine recurrent uveitis in German warmblood horses[J].PLoS One,2013,8(8):e71619.
[72] METALLINOS D L,BOWLING A T,RINE J.A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome:An equine version of Hirschsprung disease[J].Mammalian Genome,1998,9(6):426-431.
[73] WIJNBERG I D,OWCZAREK-LIPSKA M,SACCHETTO R,et al.A missense mutation in the skeletal muscle chloride channel 1(CLCN1) as candidate causal mutation for congenital myotonia in a New Forest pony[J].Neuromuscular Disorders,2012,22(4):361-367.
[74] METZGER J,OHNESORGE B,DISTL O.Genome-wide linkage and association analysis identifies major gene loci for guttural pouch tympany in Arabian and German warmblood horses[J].PLoS One,2012,7(7):e41640.
[75] ZEITZ A,SPÖTTER A,BLAZYCZEK I,et al.Whole-genome scan for guttural pouch tympany in Arabian and German warmblood horses[J].Animal Genetics,2009,40(6):917-924.
[76] LEWIS S L,HOLL H M,STREETER C,et al.Genomewide association study reveals a risk locus for equine metabolic syndrome in the Arabian horse[J].Journal of Animal Science,2017,95(3):1071-1079.
[77] XU S,LUOSANG J,HUA S,et al.High altitude adaptation and phylogenetic analysis of Tibetan horse based on the mitochondrial genome[J].Journal of Genetics and Genomics,2007,34(8):720-729.
[78] NING T,XIAO H,LI J,et al.Adaptive evolution of the mitochondrial ND6 gene in the domestic horse[J].Genetics & Molecular Research,2010,9(1):144-150.
[79] HENDRICKSON S L.A genome wide study of genetic adaptation to high altitude in feral Andean horses of the Páramo[J].BMC Evolutionary Biology,2013,13:273.
[80] LIBRADO P,DER SARKISSIAN C,ERMINI L,et al.Tracking the origins of Yakutian horses and the genetic basis for their fast adaptation to subarctic environments[J].Proceedings of the National Academy of Sciences,2015,112(50):E6889-E6897.
[81] LIU D H,HAN H Y,ZHANG X,et al.The genetic diversity analysis in the donkey myostatin gene[J].Journal of Integrative Agriculture,2017,16(3):656-663.
[82] CHEN J X,SONG Z H,RONG M J,et al.The association analysis between Cytb polymorphism and growth traits in three Chinese donkey breeds[J].Livestock Science,2009,126(1-3):306-309.
[83] 朱文进,陈娟,关学敏,等.驴生长激素基因的克隆与分析[J].中国农业科学,2011,44(3):579-586.ZHU W J,CHEN J,GUAN X M,et al.Cloning and sequence analysis of growth hormone gene from donkey[J].Scientia Agricultura Sinica,2011,44(3):579-586.(in Chinese)
[84] 关学敏,朱文进,苏咏梅.中国家驴生长激素基因内含子2的遗传多样性分析[J].畜牧兽医学报,2011,42(6):880-884.GUAN X M,ZHU W J,SU Y M.Genetic polymorphisms of the intron 2 of GH gene in Chinese domestic donkeys[J].Acta Veterinaria et Zootechnica Sinica,2011,42(6):880-884.(in Chinese)
[85] 王颜颜,托乎提·阿及德,肖海霞,等.新疆良种驴DGAT2基因第3内含子PCR-SSCP多态性与体尺性状的相关性分析[J].石河子大学学报(自科版),2011,29(1):40-44.WANG Y Y,TUOHU T,XIAO H X,et al.PCR-SSCP polymorphism of intron 3 of DGAT2 gene of fine-breed Xinjiang donkey[J].Journal of Shihezi University(Nature Science),2011,29(1):40-44.(in Chinese)
[86] HAASE B,RIEDER S,LEEB T.Two variants in the KIT gene as candidate causative mutations for a dominant white and a white spotting phenotype in the donkey[J].Animal Genetics,2015,46(3):321-324.
[87] ABITBOL M,LEGRAND R,TIRET L.A missense mutation in melanocortin 1 receptor is associated with the red coat colour in donkeys[J].Animal Genetics,2014,45(6):878-880.
[88] LEGRAND R,TIRET L,ABITBOL M.Two recessive mutations in FGF5 are associated with the long-hair phenotype in donkeys[J].Genetics Selection Evolution,2014,46:65.
[89] ABITBOL M,LEGRAND R,TIRET L.A missense mutation in the agouti signaling protein gene (ASIP) is associated with the no light points coat phenotype in donkeys[J].Genetics Selection Evolution,2015,47:28.
[90] SUN T,LI S,XIA X,et al.ASIP gene variation in Chinese donkeys[J].Animal Genetics,2017,48(3):372-373.
[91] UTZERI V J,BERTOLINI F,RIBANI A,et al.The albinism of the feral Asinara White donkeys (Equus asinus) is determined by a missense mutation in a highly conserved position of the tyrosinase (TYR) gene deduced protein[J].Animal Genetics,2016,47(1):120-124.
[92] SELVAGGI M,DARIO C.Analysis of two single-nucleotide polymorphisms (SNPs) located in exon 1 of kappa-casein gene (CSN3) in Martina Franca donkey breed[J].African Journal of Biotechnology,2013,10(26):5118-5120.
[93] VⅡTALA S,SZYDA J,BLOTT S,et al.The role of the bovine growth hormone receptor and prolactin receptor genes in milk,fat and protein production in Finnish Ayrshire dairy cattle[J].Genetics,2006,173(4):2151-2164.
[94] 毕兰舒,肖海霞,臧长江,等.疆岳驴催乳素受体基因多态性及其与泌乳性状间的相关性分析[J].中国畜牧兽医,2017,44(1):180-185.BI L S,XIAO H X,ZANG C J,et al.Study on the relationship between the polymorphisms of PRLR gene and lactation traits in Jiangyue donkeys[J].China Animal Husbandry & Veterinary Medicine,2017,44(1):180-185.(in Chinese)
[95] 王艳萍,高帅,刘迥,等.年龄、部位对新疆驴皮中Ⅰ型胶原蛋白表达影响的研究[J].中国畜牧杂志,2017,12(53):41-44.WANG Y P,GAO S,LIU J,et al.Effect of age and site on the expression of type Ⅰ collagen in Xinjiang donkey skin[J].Chinese Journal of Animal Science,2017,12(53):41-44.(in Chinese) |