ALDH7A1和EDNRB2基因分型及其与乌骨鸡皮肤乌色度关联分析OA北大核心CSTPCD
Genotyping of ALDH7A1 and EDNRB2 Genes and Their Association with Skin Blackness in Black-bone Chickens
[目的]为进一步验证醛脱氢酶7家族成员A1(ALDH7A1)和内皮素受体B2(EDNRB2)在乌骨鸡黑色素沉积中的作用,本研究对ALDH7A1和EDNRB2基因单核苷酸多态性(SNPs)位点进行基因分型,分析其多态位点与皮肤乌色度的关联性,找出对皮肤乌色度有显著效应的SNP标记,为培育乌色度高的屠宰型乌骨鸡肉鸡的分子标记辅助育种提供参考.[方法]采用基于飞行时间质谱对丝羽乌骨鸡192个个体的ALDH7A1和EDNRB2基因SNPs位点进行基因分型,采用HaploView 4.1软件分析这些SNPs位点的连锁不平衡(LD)程度,并分析不同基因型和单倍型与皮肤亮度(L*)值的相关性.[结果]ALDH7A1基因的2个SNPs位点(rs317018616 C>A和rs15992676 T>C,分别为 SNP1 和 SNP2)和 EDNRB2 基因 2 个 SNPs 位点(rs739725493 G>A 和 rs316614064 C>T,分别为SNP3和SNP4)质谱检出率为100%,ALDH7A1基因2个SNPs位点只有2种纯合子基因型,EDNRB2基因2个SNPs位点都有3种基因型.卡方检验表明,ALDH7A1基因2个SNPs位点偏离Hardy-Weinberg 平衡(P<0.05),EDNRB2 基因 2 个 SNPs 位点均处于 Hardy-Weinberg 平衡状态(P>0.05).SNP1 位点遗传多样性较低(PIC<0.25),其他3个SNPs位点为中度多态(0.25<PIC<0.5).关联分析结果表明,4个SNPs位点不同基因型间乌骨鸡背部皮肤和胸部皮肤L*值均差异不显著(P>0.05);SNP2位点TT基因型乌骨鸡大腿部皮肤L*值显著低于CC基因型(P<0.05),SNP4位点CC和CT基因型乌骨鸡大腿部皮肤L*值显著低于TT基因型(P<0.05),SNP1和SNP3位点不同基因型间乌骨鸡大腿部皮肤L*值无显著差异(P>0.05).连锁不平衡分析表明,ALDH7A1基因SNP1和SNP2位点处于强连锁不平衡状态,SNP1-SNP2连锁后产生3种单倍型,其中AATT和CCTT单倍型乌骨鸡大腿部皮肤L*值显著低于CCCC(P<0.05),但3种单倍型个体间背部皮肤和胸部皮肤L*值均差异不显著(P>0.05).[结论]ALDH7A1和EDNRB2基因与丝羽乌骨鸡大腿部皮肤乌色度密切相关,ALDH7A1基因的AATT、CCTT单倍型和EDNRB2基因的TT基因型可作为研究丝羽乌骨鸡大腿部皮肤乌色度的候选分子标记,本研究为下一步利用分子标记辅助育种加快培育乌色度高的丝羽乌骨鸡新品种提供参考.
[Objective]In order to further verify the role of ALDH7A1 and EDNRB2 in melanin deposition in Black-bone chickens,single nucleotide polymorphisms(SNPs)of ALDH7A1 and EDNRB2 genes were genotyped,and the association between polymorphic loci and skin blackness was analyzed,to find out SNP markers that had significant effects on skin blackness.It would provide reference for marker assisted selection breeding of slaughtered Black-bone chickens with higher blackness.[Method]Genotyping of SNPs of ALDH7A1 and EDNRB2 genes in 192 individuals of Silky fowls using time-of-flight mass spectrometry analysis technology.the degree of linkage disequilibrium(LD)of these SNPs were analyzed by HaploView 4.1 software,and the association between different genotypes and haplotypes with skin brightness(L*)values was analyzed.[Result]The mass spectrometry detection rate of two SNPs in ALDH7A1(rs317018616 C>A(SNP1)and rs15992676 T>C(SNP2))and two SNPs in EDNRB2 genes(rs739725493 G>A(SNP3)and rs316614064 C>T(SNP4))were 100%.There were only two homozygous genotypes at the two SNPs of ALDH7A1 gene,while there were three genotypes at both SNPs of EDNRB2 gene.Chi-square test showed that the two SNPs of ALDH7A1 gene deviated from Hardy-Weinberg equilibrium(P<0.05),while the two SNPs of EDNRB2 gene were in Hardy-Weinberg equilibrium(P>0.05).The genetic diversity of SNP1 was low(PIC<0.25),and the other three SNPs were moderately polymorphic(0.25<PIC<0.5).Association analysis showed that there was no significant difference in L*values of the back skin and breast skin among different genotypes of the four SNPs(P>0.05).The thigh skin L*value of TT genotype at SNP2 was significantly lower than that of CC genotype(P<0.05).The thigh skin L*values of CC and CT genotypes at SNP4 were significantly lower than that of TT genotype(P<0.05).There was no significant difference in thigh skin L*values between different genotypes at SNP1 and SNP3(P>0.05).The analysis of linkage disequilibrium indicated that SNP1 and SNP2 of ALDH7A1 gene were in a strong linkage imbalance state,three haplotypes were generated after SNP1-SNP2 linkage.The thigh skin L*values of AATT and CCTT haplotypes of Black-bone chickens were significantly lower than that of CCCC haplotype(P<0.05),but there was no significant difference in L* values of the back skin and breast skin among the three haplotypes(P>0.05).[Conclusion]The ALDH7A1 and EDNRB2 gene were closely related to the thigh skin blackness.The AATT and CCTT haplotypes of ALDH7A1 gene and TT genotype of EDNRB2 gene could be used as a candidate molecular marker for studying the thigh skin blackness in Silky fowls.It would provide a theoretical reference for using molecular marker assisted breeding to accelerate the cultivation of new Silky fowls with higher blackness.
屠云洁;赵伟东;郑国庆;栾德琴;章明;巨晓军;刘一帆;单艳菊;姬改革;邹剑敏;束婧婷
江苏省家禽科学研究所,江苏省家禽遗传育种重点实验室,农业农村部畜禽资源(家禽)评价利用重点实验室,扬州 225125泰和凤升农牧科技有限公司,吉安 343700国家知识产权局专利局专利审查协作江苏中心,苏州 215163
畜牧业
乌骨鸡ALDH7A1基因EDNRB2基因乌色度SNP
Black-bone chickensALDH7A1 geneEDNRB2 geneblacknessSNP
《中国畜牧兽医》 2024 (007)
2923-2932 / 10
江苏省自然科学基金青年基金项目(BK20230729);江苏省自然科学基金(BK20211121);江苏省种业振兴揭榜挂帅项目(JBGS[2021]107);现代农业产业技术体系建设专项资金(CARS-41);江苏省农业自主创新基金项目(CX(21)2011-1);扬州市现代农业项目(YZ2021029)
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