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Genetic polymorphisms of growth hormone (GH) gene in Kacang goat population based on polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) identification

机译:基于聚合酶链反应-限制性片段长度多态性(PCR-RFLP)鉴定的加康山羊种群生长激素(GH)基因遗传多态性

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KacanggoatisasmallruminantnativefromIndonesiaandspreadwidelyinseveralSoutheastAsiancountries,andhasbecomepartoftheworld#8217;sbiodiversity.GrowthHormone(GH)ingoatisaproteinsecretedfromanteriorhipophysebysomatrotopcellsanditsformationprocessunderthecontrolofGHgene.Itsmainfunctionistostimulatethegrowthofbone,muscleandfatmetabolism.ThepurposeofthisstudyistoidentifytheGHgenepolymorphisminKacanggoatwithPolymeraseChainReaction-RestrictionFragmentLengthPolymorphism(PCR-RFLP)methods.Atotalof168bloodsamplesfromKacanggoatintworegionsofIndonesia(GorontaloandSouthSulawesiprovince)wereextractedbyusingDNAextractionkittocollectwholeDNAgenome.AmplificationandgenotypingofGHgenewasperformedusingPCR-RFLPusingtheHaeIIIrestrictionenzyme.Theresultsobtainedtwokindsofgenotypes,withtheAAgenotypefrequencies(0.095)andAB(0.904).ThefrequencyofalleleA(0.547)andB(0.452)indicateapolymorphismintheGHA781GlocusinKacanggoat.Theobserved(Ho)andexpected(He)heterozygosityvaluewererespectively0.0904and0.496.GHallelesdistributioninKacanggoatpopulationswerenotinHardy-Weinbergequilibrium.Basedonstatisticalanalysis,thereisnodifferencebetweenbodysizeofgenotypeAAandAB.TheresultsofthisstudycanbeusedasinitialinformationinformulatingastrategyforKacanggoatbreedingbyutilizingMarkerAssistedSelection(MAS).
机译:KacanggoatisasmallruminantnativefromIndonesiaandspreadwidelyinseveralSoutheastAsiancountries,andhasbecomepartoftheworld#8217; sbiodiversity.GrowthHormone(GH)ingoatisaproteinsecretedfromanteriorhipophysebysomatrotopcellsanditsformationprocessunderthecontrolofGHgene.Itsmainfunctionistostimulatethegrowthofbone,muscleandfatmetabolism.ThepurposeofthisstudyistoidentifytheGHgenepolymorphisminKacanggoatwithPolymeraseChainReaction-RestrictionFragmentLengthPolymorphism(PCR-RFLP)methods.Atotalof168bloodsamplesfromKacanggoatintworegionsofIndonesia(GorontaloandSouthSulawesiprovince)wereextractedbyusingDNAextractionkittocollectwholeDNAgenome.AmplificationandgenotypingofGHgenewasperformedusingPCR-RFLPusingtheHaeIIIrestrictionenzyme.Theresultsobtainedtwokindsofgenotypes,withtheAAgenotypefrequencies(0.095)andAB(0.904).ThefrequencyofalleleA (0.547)和B(0.452)在加蓬山羊GHA781群中的印度茶多态性。分别观察到(Ho)和预期(He)杂合度值分别为0.0904和0.496.Galleles分布离子交换蛋白在加康果族种群中的维雷德平衡哈迪-温伯格平衡。基于统计学的分析,基因型AA和AB的体型之间没有区别。因此,可以利用原始的信息通过使用标记辅助选择(MAS)来对加香果育种策略进行初步的研究。

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