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用于小麦A和B基因组基因分型的EST衍生微卫星标记的分离

Isolation of EST-derived microsatellite markers for genotyping the A and B genomes of wheat.

作者信息

Eujayl I., Sorrells M. E., Baum M., Wolters P., Powell W.

机构信息

ICARDA, Germplasm Program, P.O. Box 5466, Aleppo, Syria.

出版信息

Theor Appl Genet. 2002 Feb;104(2-3):399-407. doi: 10.1007/s001220100738.

Abstract

Genetic variation present in 64 durum wheat accessions was investigated by using three sources of microsatellite (SSR) markers: EST-derived SSRs (EST-SSRs) and two sources of SSRs isolated from total genomic DNA. Out of 245 SSR primer pairs screened, 22 EST-SSRs and 20 genomic-derived SSRs were polymorphic and used for genotyping. The EST-SSR primers produced high quality markers, but had the lowest level of polymorphism (25%) compared to the other two sources of genomic SSR markers (53%). The 42 SSR markers detected 189 polymorphic alleles with an average number of 4.5 alleles per locus. The coefficient of similarity ranged from 0.28 to 0.70 and the estimates of similarity varied when different sources of SSR markers were used to genotype the accessions. This study showed that EST-derived SSR markers developed in bread wheat are polymorphic in durum wheat when assaying loci of the A and B genomes. A minumum of ten EST-SSRs generated a very low probability of identity (0.36x10(-12)) indicating that these SSRs have a very high discriminatory power. EST-SSR markers directly sample variation in transcribed regions of the genome, which may enhance their value in marker-assisted selection, comparative genetic analysis and for exploiting wheat genetic resources by providing a more-direct estimate of functional diversity.

摘要

利用三种微卫星(SSR)标记来源,对64份硬粒小麦材料的遗传变异进行了研究:来源于EST的SSR(EST-SSRs)以及从总基因组DNA中分离出的两种SSR来源。在筛选的245对SSR引物中,22个EST-SSRs和20个基因组来源的SSR具有多态性,并用于基因分型。EST-SSR引物产生了高质量的标记,但与其他两种基因组SSR标记来源相比,其多态性水平最低(25%),而其他两种基因组SSR标记来源的多态性水平为53%。42个SSR标记检测到189个多态性等位基因,每个位点平均有4.5个等位基因。相似系数在0.28至0.70之间,当使用不同来源的SSR标记对材料进行基因分型时,相似性估计值有所不同。本研究表明,在对A和B基因组的位点进行检测时,面包小麦中开发的来源于EST的SSR标记在硬粒小麦中具有多态性。至少十个EST-SSRs产生了极低的一致性概率(0.36×10⁻¹²),表明这些SSR具有非常高的鉴别力。EST-SSR标记直接对基因组转录区域的变异进行采样,通过提供更直接的功能多样性估计,这可能会提高它们在标记辅助选择、比较遗传分析以及开发小麦遗传资源方面的价值。

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